Team:Freiburg Bioware/testpage

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1 76.Labortag 01.08.2010
- 1.1 Picking clones of pSB1C3_CMV
2 77.Labortag 02.08.2010
3 78.Labortag 03.08.2010
4 79.Labortag 04.08.2010
5 80.Labortag 05.08.2010
6 81.Labortag 06.08.2010
7 82.Labortag 07.08.2010
8 83. Labortag 08.08.2010
9 84. Labortag 09.08.2010
10 85. labday 10.08.2010
11 86. labday 11.08.2010
12 87. labday 12.08.2010
13 88. labday 13.08.2010
14 89. labday 14.08.2010
15 90. labday 15.08.2010

76.Labortag 01.08.2010

Picking clones of pSB1C3_CMV

Investigator: Bea

Comments: Trafo was performed friday, and trafo plate were incubated over night. Clones need to be picked in order to perform Mini-Prep

Bacterial strain used: XL1-B
Two clones were picked of trafo plate
Inoculating of 10 mL DYT medium containing 10µL chloramphenicol
Put in 37°C room on rotary shaker

77.Labortag 02.08.2010

Sequenzing of pSB1C3_RFC25_longlinker, pSB1C3_RFC25_SEG, pSB1C3_RFC25_GSAT

Investigator: Jessica

Comments: Linkers (we got from Gerrit) we cloned in the RFC25-standard (pSB1C3_RFC25). Result looks good, linkers are in the vector pSb1C3_RFC25

pSB1C3_RFC25_longlinker P105 und P106
pSB1C3_RFC25_SEG P107 und P108
pSB1C3_RFC25_GSAT P109 und P110

Freiburg10 Sequence alignment longlinker.jpg

Sequencing of pGA14_Prefix-leftITR

Investigator: Hanna

Eventually GATC partially managed to sequence pGA14_Prefix-left ITR clone 1 and 2.
The sequencing results were better than before but in the ITR region still not evaluable due to the strong secondary structures.

It seemed that, despite of successful insertion of the RFC10-Prefix, something went wrong because there were 2 bases missing in the NotI restriction site. But by having a closer look, it became obvious that the Geneious misinterpreted the chromatogram and overlaid the peaks of the missing bases.

For the first time sequencing of parts of the 3' end worked: The remaining NotI restriction site, which was already eliminated this week and also the "backbone-PstI" can be seen:

Sequencing of very GC-rich regions :) :) :)

Sequencing of clone 4 delivered that the ITR and the RFC10-Prefix were not inserted in the vector. The RFC25 standard of the multiple cloning site is still in the plasmid:

Therefore clone 4 was dicarded from the plasmid- and glycerol stock.

Repetition of test digestion pSB1C3_CFP SDM SspI and PvuII

Investigator: Jessica

buffer used: 2; Restriction-enzymes used: Enzyme 1: SspI ; Enzyme 2: PvuII

Plasmids (all: ~ 700 ng/µL):

pSB1C3_CFP P51.1
pSB1C3_SDM_SspI P125
pSB1C3_SDM_PvuII P129
pSB1C3_SDM_PvuII P131

Components	Mastermix	P125/µL	P51.1.1/µL	P129/µL	P131/µL	P51.1.2/µL
DNA	-	2,4	2,3	1,6	5,3	5,3
BSA (10x)	6	1	1	1	1	1
Buffer 2 (10x)	6	1	1	1	12	1
Enzyme 1 SspI (68)	-	1	1	-	-	-
Enzyme 2 PvuII (50)	-	-	-	1	1	1
H₂O	-	4,6	4,7	5,4	1,7	1,7
Total volume	12	10	10	10	10	10

Incubation: 65 minutes

Agarosegel
0.45 g Agarose, 50 ml TEB (0,5 %), 3 µL GELRED, at 115 Volt, running time: 45 minutes

Marker: GeneRuler ladder mix (6x)

	Marker	P125	P51.1 SspI	-	P129	P131	P51.1 PvuII
Lane	7 µL	10 µL	10 µL	-	10 µL	10 µL	10 µL

P125 isn't cut, therefore you see the bands for supercoiled, nicked and relaxed
P51.1 is cut once, therefore you can see a faster running band
P129 and P131 should be cut once because of the PvuII in the CFP but there is another band we can't identify
P51.1 should be cut two times but there is also another unidentified band

perhaps there is another PvuII in the vector we can't find (???)

Comments: SDM of SspI is ready! SDM of PvuII looks confusing because of the lower band. P 129 will be sequenced but this doesn't solve this problem. there has to be one more rs we don't know, perhaps. we will check it...anywise

Mini-Prep and Test digestion of pSB1C3_CMV

Investigator: Kerstin
Nanodrop

pSB1C3_CMV clone1: 157,6 ng/µl P145
pSB1C3_CMV clone2: 155,6 ng/µl P146

Test digestion 900ng DNA

components	P145 /µl	P146 /µl
DNA	5,7	5,8
BSA (10x)	1,5	1,5
Buffer 4 (10x)	0,5	0,5
Enzyme 1: XbaI	0,5	1,5
Enzyme 2: PstI	0,5	0,5
H₂O	5,3	5,2
Total volume (e.g. 15,20,25,30 µl)	15	15

agarose gel: 1,5%, digestion: 90 minutes, 37°C

P145 is sent for sequencing with Reverse Primer (VR2)

Comments:Results look good. CMV has the expected size (~ 662bp)

</p>

Sent for sequencing

Investigator: Jessica
Hanna

P145 left ITR

Primer: GATC_std_pQE-FP and GATC_std_m13-FP

P150 right ITR

Primer: GATC_std_pQE-FP and GATC_std_m13-FP

Anissa

P136 pSB1C3_hgh

Primer: O51_Reverse Primer (VR2)

P139 pAAV_BamHI

Primer: O36_Rep_1250_rev

P143 pAAV_RC_SalI

Primer: O53_Rep_1250_for

P141 pGL3_QTERT

Primer: GATC_std_pTal-FP

P133 pSB1C3_betaGlobin

Primer: O51_ReversePrimer (VR2)

P145 pSB1C3_CMV

Primer: O51_ReversePrimer (VR2)

Jessica

P129 pSB1C3_SDM_PvuII

Primer: GATC_std_pTeSp-2

Preparation of competent E.coli

Investigator: Jessica

15ml DYT was prepared with 15µl tetracycline and inoculate with XL1B
10ml DYT w/o antibiotics was prepared and inoculate with BL21 (just for glycerol stock, no competent cells)

both were incubate over night in 37°C room

Last Mini-Prep and test digestion of ITRs

Investigator: Hanna

Plasmid Mini-Prep

new vector name: pGA14_RFC10_leftITR and pGA14_RFC10_rightITR

Glycerol Stocks
pGA14_RFC10_leftITR

	Clone 1	Clone 2	Clone 3
Bacteria strain	XL1blue	XL1blue	XL1blue
Plasmidname	pGA14_RFC10_leftITR	pGA14_RFC10_leftITR	pGA14_RFC10_leftITR
Date	2.8.10	2.8.10	2.8.10
given glycerol-stock no.	B115	B116	B117
given plasmid no.	P147	P148	P149

pGA14_RFC10_rightITR

	Clone 1	Clone 2	Clone 3
Bacteria strain	XL1blue	XL1blue	XL1blue
Plasmidname	pGA14_RFC10_rightITR	pGA14_RFC10_rightITR	pGA14_RFC10_rightITR
Date	2.8.10	2.8.10	2.8.10
given glycerol-stock no.	B112	B113	B114
given plasmid no.	P150	P151	P152

Test digestion

buffer used: 4 ; Restriction-enzymes used: Enzyme 1 XbaI ; Enzyme 2 SpeI
Plasmid: pGA14_RFC10_leftITR:
- Given Plasmid-Number: P147; DNA concentration: 240.22 ng/µL ;
- Given Plasmid-Number: P148; DNA concentration: 268.97 ng/µL ;
- Given Plasmid-Number: P149; DNA concentration: 234.16 ng/µL ;

Plasmid: pGA14_RFC10_rightITR:
- Given Plasmid-Number: P150; DNA concentration: 221.71 ng/µL ;
- Given Plasmid-Number: P151; DNA concentration: 191.13 ng/µL ;
- Given Plasmid-Number: P152; DNA concentration: 215.14 ng/µL ;

Components	P147 Volume/µL	P150 Volume/µL
DNA	4.2	4.5
BSA (10x)	1	1
Buffer no. 4 (10x)	1	1
Enzyme 1 XbaI	0.5	0.5
Enzyme 2 SpeI	0.5	0.5
H₂O	2.8	2.5
Total volume	P147	P150

Incubation: 1 h

Agarose-Gel:

0.83 g Agarose, 53 mL TBE (1.57%), 3 µL GELRED, at 115 Volt, running time: 45 minutes

Sample	Sample/µl]	Loading dye (5x)/µl	Expected size 1 (Geneious)	Expected size 2 (Geneious)
P147	10 µl	2 µl	157 bp	2902 bp
P150	10 µl	2 µl	156 bp	2903 bp

Marker: GeneRuler ladder mix

	Marker /µL	Sample P147 /µL	Sample P150 /µL
Lane	6.5	12	12

Test digestion delivered positive results for both ITRs: The expected fragment sizes (156 resp. 157 bp) could be detected in the referring range between the 100 and 200 bp marker nucleotides:

Comment: In order to verify the results, P147 and P150 were sent for sequencing. Because sequencing never worked before, they will be sequenced under special conditions this time.

BioBrick production: mGMK in pSB1C3

Investigator: Stefan
Backbone taken from:

pSB1C3_CFP (P51.2): 151,1 ng/µl

Insert taken from:

pAAV_RFC25_mGMK (P100): 411,3 ng/µl

components	pSB1C3_CFP(P51.2) /µl	pAAV_RFC25_mGMK (P100) /µl
DNA	8	5
BSA (10x)	2	2
Buffer 4 (10x)	2	2
XbaI	1	1
AgeI	1	1
H₂O	6	9
Total volume	20	20

1% Agarose gel
3 µl Gelred
7 µl DNA-Ladder-Mix
115 Volt, running time: 50 minutes

Afer 50 minutes a picture (see below) was taken. Because there was no clear pattern (two bands) for the pSB1C3 backbone, the band of the insert mGMK was cut out and the gel ran another 20 minutes. After that, there were still two bands. Both were cut out and it was continued with two possible backbones. They were labeled vector (lower) and vector (upper).

Sample/µl	Expected size/bp
Vector pSB1C3	2082
Insert mGMK	603

weight of insert mGMK gel extract: 0,17 g
weight of vector (lower) pSB1C3 gel extract: 0,08 g
weight of vector (upper) pSB1C3 gel extract: 0,09 g

Nanodrop

insert mGMK : 4,13 ng/µl
vector (lower) pSB1C: 5,47 ng/µl
vector (upper) pSB1C: 0,60 ng/µl => for calculation of ligation approach calculated with 1 ng/µl

Ligation

vector (lower) : insert - 4,16 µl : 4,84 µl
vector (upper) : insert - 7,43 µl : 1,57 µl

Transformation Two approaches were prepared, one for each vector and put in 37 °C room overnight.

Sequencing results of SDM Rep 68 & 78

Investigator: Hanna and Volker
The sequencing results delivered that the PstI restriction sites of Rep 68 and Rep 78 were successfully deleted via side-directed mutageneis:

Sequencing results of SDM Rep 68 & 78
Rep 68	Rep 78

78.Labortag 03.08.2010

Results of sequencing pSB1C3_CFP_SDM_PvuII

Investigator: Jessica
SDM of PvuII:

PvuII is succesfully deleted in the vector pSB1C3_RFC25_CFP

Repetition of the quickchange site-directed mutagenesis of pAAV_RC_1.1_SalI

Investigator: Kerstin,Anissa

Comments: Sequenzing revealed no mutagenesis of SalI in pAAV_RC_1.1_SalI, so SDM now will be repeated.

PCR-reaction:

Volume / µl	ingredients	recommended /µl
2,5	10X Pfu Ultra II buffer	2,5
4,18	template (~10 ng)	4,18 of 1:100 dilution
0,58	forward primer: O68	62,5 ng
0,58	reverse primer: O69	62,5 ng
0,5	dNTP	250 µM each dNTP
16,16	H₂O
0,5	PfuUltra II fusion (1.25)

PCR program:

Rounds	temperature/ °C	Time
1	95	2 minutes
20	95	30 seconds
20	80,4	1 minute
20	68	7,5 minutes

Plasmid was transformed into BL21 cells. Clones have to be picked tomorrow.

Comments:NO CLONES, trafo didn't work, because annealing temperature was totally to high! (80,4 °C instead of 55°C) annealing temperature should always be 55°C (in case of troubleshooting temperature can be increased up to MAX. 68°C !)

PCR for Biobrickproduction of Rep 40, 52, 68, 78 and APP

Investigators: Volker, Anna

Aim of the experiment: We wanted to produce biobricks from the expression plasmids Rep40ex, Rep52 ex, the Rep 68 and 78 in which the PstI at position 310 was silenced and the AAP. This was performed by a PCR with primes that annealed to the ends of the later biobrick but also contained restriction sites that can be cut afterwards and cloned into pSB1C3.

Plasmids used as template:

Rep_68_ex (p119): c = 470,6 ng/µl
Rep_78_(p122): c = 201,08 ng/µl
Rep_40_(p22.2): c = 673,1 ng/µl
Rep_52_(p23.2): c = 532,22 ng/µl
pAAV-RC containing AAP ORF (p50): c = 378,5 ng/µl

Primer used:

For Rep_40_ex: Praefix_40_52_ex & Suffix_40_68_ex
For Rep_52_ex: Praefix_40_52_ex & Suffix_52_78_ex
For Rep_68_ex: Praefix_68_78_ex & Suffix_40_68_ex
For Rep_78_ex: Praefix_68_78_ex & Suffix_52_78_ex
For AAP_ex: Praefix_AAP_ex & Suffix_AAP_ex

PCR:

(was performed following the standard protocol)

Ingredients	Volume / µl	Rep68	Rep78	Rep40	Rep52	AAP
5X Phusion HF buffer	10
10 mM dNTP mix	1
forward primer:	2,5
reverse primer:	2,5
DNA Template	***	4,2 µl	1 µl	2,9 µl	3,8 µl	5,3 µl
Phusion Polymerase	0,5
H₂O	***	28,3 µl	31,5 µl	29,6 µl	28,7 µl	27,2 µl
Total volume	50

PCR program:

PCR Program	temperature/ °C	Time	Rep40	Rep50	Rep68	Rep78	AAP
1	98	1min
2	98	15s
8x	***	25s	63°C	62°C	63°C	62°C	64°C
3	72	***	15s	18s	24s	27s	10s
4	98	15s
17x	***	25s	68°C	66°C	68°C	64°C	68°C
5	72	***	15s	18s	24s	27s	10s
6x	72	5min
Hold	4

Five µl of PCR-product were used for an analytical gel to see if the PCR worked.

BioBrick production for Rep and AAP
Alalytical gel	Praeparative gel

Comment: The result is that the PCR worked for the longer Rep proteins (68&78) with which a Quick-change was performed to remove the PstI(310) but not with the constructs for the smaller Rep variants (40&52) that were recieved from PD Kleinschmidt. As the longer Rep variants the AAP PCR Reaction also resulted in a PCR-product of the expected size. Unfortunately there were a secondary band of ~90bp for Rep_68_ex. For this reason we performed a praeparative gel and decided to cut the bands of all PCR products.

The bands marked in the gel picture were cut and a gel extraction was performed.

Gel extraction

Gel measurement:

Sample	Weight	Volume	Concentration
Rep_68_ex	0,1 g	20 µl	17,6 ng/µl
Rep_78_ex	0,15g	20 µl	80,6 ng/µl
AAP_ex	0,19 g	20µl	77,78 ng/µl

Continuation of preparation of competent E.coli

Investigator: Jessica
preparation of competent XL1blue was finished according to the standard protocol

aliquots of 60µl (to use for 1 trafo) are stored in -80°C freezer

Sequencing of pSB1C3

Investigator: Jessica

Comments: We sent for sequencing pSB1C3_RFC25_longlinker (P105) to check the strange result of the test digestion of pSB1C3_SDM_PvuII(01.08.10.
pSB1C3_SDM_PvuII is too long for sequencing wherefore we sent pSB1C3_RFC25_longlinker because the longlinker just have 54kb (bp, nicht kb (Volker) (necessary is just the backbone we don't have.

Primer:

RESgen-241698
Reverse primer (VR2)
o_F1-fw (from Gerrit)

Design of Primer for p5 Promoter WT and TATA-less BioBrick production

Investigator: Hanna

79.Labortag 04.08.2010

Cloning of right ITR and left ITR into pSB1C3_RFC25_CFP

Intention: Get biobricks ready.
Investigator: Patrick
pGA14_lITR_RFC10 (P147), pGA14_rightITR (P150) and pSB1C3_RFC25_CFP (P51.1) were digested with EcoRI and PstI (Buffer 4) according to the standard protocol. Digestion Time: 80 minutes.
GelRun: 1% Agarose Gel. Expected results (from left to right):

pSB1C3_RFC25_CFP: about 2100 bp and 800 bp.
pGA14_leftITR_RFC10: the size of the insert should be 135 bp.
pGA14_rightITR_RFC10: the size of the insert should be 138bp.

The mutual vector (now without CFP) and inserts (left ITR and right ITR) were cut out. The gelextraction was performed according to the standard protocol. DNA concentration of the extracts:

pSB1C3_RFC25_CFP: 2,9 ng/µl
left ITR: 1,4 ng/µl
right ITR: 2,0 ng/µl

The Quick Ligation was not performed according to the standard protocol:

left ITR + pSB1C3: 5µl Buffer, 1 µl Quick-Ligase, 2,5 µl left ITR, 1,5 µl pSB1C3_RFC25.
right ITR + pSB1C3: 5µl Buffer, 1 µl Quick-Ligase, 2,5 µl right ITR, 1,5 µl pSB1C3_RFC25.

Transformation: performed according to the standard protocol (BL21). The cells were plated on a agar plate with chloramphenicol. The clones will be picked tomorrow.

Cloning of SDM SspI and SDM PvuII

Investigator: Jessica

Vector: name: pSB1C3_SDM_SspI P125
Insert: name: pSB1C3_SDM_PvuII P129
new vector name: pSB1c3_SDM_SspI/PvuII P157
buffer used: 4 ; Restriction-enzymes used: Enzyme 1 (no. Lab: 141) BstI ; Enzyme 2 (no.Lab: 144) BpmI
DNA concentration (vector): 321,9 ng/µl ; DNA concentration (insert): 308,4 µg/µl

components	volume of pSB1C3_SDM_SspI /µl	volume of pSB1C3_SDm_PvuII /µl
DNA	4,66	4,87
BSA (10x)	2	2
Buffer 4 (10x)	2	2
Enzyme BstI (no.Lab:141)	1	1
Enzyme BpmI (no.Lab:144)	1	1
H2O	9,34	9,13
Total volume (e.g. 15,20,25,30 µl)	20	20

0,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 130 Volt, running time:45

Loading plan for agarose gel:
Marker used: GeneRuler ladder mix (Fermentas)

	Marker	Sample 125, 20µl	Sample 129, 20µl
Lane	1	3	5

Results: digesttemperature of BstI is 55°C, plasmid was just digested at 37°C... :( (

2nd Repetition of Quickchange site-directed mutagenesis of pAAV_RC_1.1_SalI

Investigator: Kerstin, Anissa

Comments: Last trafo didn't work. Annealing temperature was to high (80,4°C instead of 55°C)

Two approaches were made (short and long PCR:

PCR-reaction:

Volume / µl	ingredients	recommended /µl
2,5	10X Pfu Ultra II buffer	2,5
1,83	template (~10 ng): p139 (c: 546,97 ng/µl)	1,83µl of 1:100 dilution
0,58	forward primer: O68	62,5 ng
0,58	reverse primer: O69	62,5 ng
0,5	dNTP	250 µM each dNTP
18,51	H₂O
0,5	PfuUltra II fusion (1.25)

PCR program (long):

Cycles	temperature/ °C	Time
1	95	2 minutes
20	95	30 seconds
20	55	1 minute
20	68	7,5 minutes

PCR program (short):

Cycles	temperature/ °C	Time
1	95	2 minutes
20	95	30 seconds
20	55	1 minute
20	68	4 minutes

Plasmids were transformed into BL21 cells. Clones have to be picked tomorrow.

Mini-Prep of pSB1C3_mGMK

Investigator: Chris W., Bea

Vector name: pSB1C3_mGMK upper band 1.1 and pSB1C3_mGMK upper band 1.2 and pSB1C3_mGMK lower band 2.1 and pSB1C3_mGMK lower band 2.2

Mini-Prep following the standart Protokoll

P153 = pSB1C3_mGMK upper band 1.1 = 248,3 ng/µl

P154 = pSB1C3_mGMK upper band 1.2 = 251,6 ng/µl

P155 = pSB1C3_mGMK lower band 1.1 = 263 ng/µl

P156 = pSB1C3_mGMK lower band 1.2 = 235,2 ng/µl

Test digestion:

Perfomed with 15 µL of total volume with all four clones

	Mastermix/µL	P153/µL	P154/µL	P155/µL	P156/µL
DNA	-	3,5	3,5	3,5	3,5
BSA (10x)	7,5	4	4	4	4
Buffer 4 (10x)	7,5
Enzyme XbaI	2,5
Enzyme AgeI	2,5
H2O	-	7,5	7,5	7,5	7,5
Total volume	15	15	15	15	15

All four samples were loaded on a 1% agarose gel
P153 = pSB1C3_mGMK upper band 1.1
P154 = pSB1C3_mGMK upper band 1.2
P155 = pSB1C3_mGMK lower band 1.1
P156 = pSB1C3_mGMK lower band 1.2

Sequencing:

Plasmid used: P156: pSB1C3_mGMK lower band 1.2
Primer used: VR-2
Tube name: Bea_1

cell culture

Investigator: Adrian
Plan for the next virus production procedures
The Motivation: investigation of the influence of different GOI amounts.
The Plan: keep rep/cap and pHelper amount stable (3,3 µg each => 6,6 µg), differ the GOI (YFP) amount in each stock.
Viral Stocks:

3,3 µg YFP + 3,3 µg pHelper + 3,3 rep/cap
10 µg YFP + 3,3 µg pHelper + 3,3 rep/cap
20 µg YFP + 3,3 µg pHelper + 3,3 rep/cap

3,3 µg pHelper + 3,3 rep/cap (without GOI !!!)

one GMK_TK clone (with the confirmed sequence) + 3,3 µg pHelper + 3,3 rep/cap

Transduction plan

five 6-well-plates wille be transduced

A	150µl AAV stock 1	300µl AAV stock 1	control no Virus
B	150µl AAV stock 2	300µl AAV stock 2	150µl AAV without GOI

Repetition of cloning of SDM SspI and SDM PvuII

Investigator: Jessica

Vector: name: pSB1C3_SDM_SspI P125
Insert: name: pSB1C3_SDM_PvuII P129
new vector name: pSB1C3_RFC25_SDM_SspI/PvuII P157
buffer used: 4 ; Restriction-enzymes used: Enzyme 1 (no. Lab: 141) BtsI ; Enzyme 2 (no.Lab: 144) BpmI
DNA concentration (vector): 321,9 ng/µl ; DNA concentration (insert): 308,4 µg/µl

components	volume of pSB1C3_SDM_SspI /µl	volume of pSB1C3_SDm_PvuII /µl
DNA	4,66	4,87
BSA (10x)	2	2
Buffer 4 (10x)	2	2
Enzyme ClaI (no.Lab:152)	1	1
Enzyme BpmI (no.Lab:144)	1	1
H2O	9,34	9,13
Total volume (e.g. 15,20,25,30 µl)	20	20

incubation time: 1,5h
0,5 g Agarose,50 ml TBE (1%), 3 µl GELRED (gel was shared with Anna) , at Volt, running time:

Loading plan for agarose gel:
Marker used: GeneRuler ladder mix (Fermentas)

	Marker	Sample 125, 20µl	Sample 129, 20µl
Lane	1	3	5

This appproach also didn't work, same result. the guess is that BpmI doesn't work anymore. will be repeated by Chris W. on 05.08.10. the result will show that the guess is right and BpmI from labstock is changed out with a new one.

Test transformation of XL1 competent cells

Investigator: Kira

Test transformation was performed in order to test the efficiency of produced chemical competent XL1 blue cells.

2 plates were prepared: one with 50 pg and the second with 100 pg pUC 18 plasmid (50 pg/㎕) 50 pg plate: 1 ㎕ pUC + 50 ㎕ XL1B cells 100 pg plate: 2 ㎕ pUC + 50 ㎕ XL1B cells

Transformation was performed according to the standard protocol and the plates were incubated at 37 C.

Sequencing results of ITRs

Investigator: Hanna
8 sequencing files were analyzed "per hand" base by base. Alignments (will be inserted soon) delivered that the right ITR is 100% OK and was successfully converted into the RFC10 BioBrick standard.

The sequencing and alignments of the left ITR delivered that a 15 bp fragment in the middle of the sequence is lacking. Therefore further test digestions have to be performed. Nevertheless also this ITR was successfully converted into the RFC10 BioBrick standard. Secondary structure analysis showed that the stemloop-structure will be nevertheless forming. We will try to test whether the referring fragment is also missing in the pAAV_MCS. If it's also lacking there we will continue with this ITR and test whether it functions.

Cloning of Rep68, Rep78 and AAP into pSB1C3

Investigator: Anna

Comments: The PCR of Rep 40/52 didn't work (see 03.08), whereas the PCR of Rep 68/78 and AAP was succesful. Ligation was done with two different samples of pSB1C3 (see agarose gel). Samples from digestion and from ligation are stored in the 4°C freezer.

Digestion of PCR products and vector:

components	PCR product /µl	vector /µl
DNA	19	10
BSA (10x)	3	3
Buffer 4 (10x)	3	3
Enzyme XbaI	1	1
Enzyme SpeI	1	1
H2O	3	12
Total volume (e.g. 15,20,25,30 µl)	30	30

Comments: Digestion was done with XbaI and SpeI, it has to be checked if the inserts are cloned into the vector in the right orientation.

Purification of Rep68, 78 and AAP:

For the purification 95 µl of buffer PBI was used.

c(Rep68)= 17,6 ng/µl
c(Rep78)= 80,60 ng/µl
c(AAP)= 77,78 ng/µl

Gelextraction of pSB1C3_RFC25_CFP:

0,5 g Agarose,50 ml TBE (1%), 3 µl GELRED , at 115 Volt, running time:55
5µl loading dye (6x) for the sample, Marker: GeneRuler ladder mix (Fermentas)

c(pSB1C3)= 2,87 ng/µl
c(pSB1C3_2)= 9,46 ng/µl

Quickligation of PCR products and vector:

For the Ligation 10µl buffer (2x) and 1µl Quickligase were used.

	Sample-no.	vector /µl	insert /µl
pSB1C3 + Rep68	1.1	6,51	2,4
pSB1C3_2 + Rep68	1.2	3,9	5,02
pSB1C32 + Rep78	2.1	8,2	0,8
pSB1C3_2 + Rep78	2.2	6,82	2,18
pSB1C3 + AAP	3.1	8,71	0,92
pSB1C3_2 + AAP	3.2	8,1	0,9
Total volume (e.g. 15,20,25,30 µl)	9

Transformation:

The transformation was done following the standard protocol using B21 cells.

80.Labortag 05.08.2010

New LB Agar was prepared.

Investigator: Patrick

Sequenc analysis of BioBricks: CMV, hGH and beta globin

Investigator: Bea

Comments: Sequence analysis of three BioBricks which were cloned into the iGEM standard plasmid pSB1C3. Cloning of this three plasmids were performed at:

Sequencing results of pSB1C3_CMV:

Plasmid sent for sequencing:
Primer used: VR-2
Results: Sequence read looks good. The incorporation of the PCR product can be confirmed. It can be seen that the insert is in the RFC10 standard and prefix and suffix have the right sequence. Therefore, this BioBrick can be send to the registry and used for BioBrick assembly.But: there is a mutation in the termintor (sequence picture do not show this mutation)

Sequencing results of pSB1C3_hGH:

Plasmid sent for sequencing:
Primer used: VR-2
Results: Sequence read looks good. The incorporation of the PCR product can be confirmed. It can be seen that the insert is in the RFC10 standard and prefix and suffix have the right sequence. Therefore, this BioBrick can be send to the registry and used for BioBrick assembly.

http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/images/e/e1/Freiburg10_Sequence_analysis_of_PSB1C3_betaglobin.jpg

Sequencing results of pSB1C3_hGH:

Plasmid sent for sequencing:
Primer used: VR-2
Results: Sequence read looks good. The incorporation of the PCR product can be confirmed. It can be seen that the insert is in the RFC10 standard and prefix and suffix have the right sequence. Therefore, this BioBrick can be send to the registry and used for BioBrick assembly.

http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/images/4/44/Freiburg10_Sequence_analysis_of_PSB1C3_hGH.jpg

Cellculture

Investigator: Adrian

The Motivation: Transfection
The Action: HEK cells were split into four T75 flasks
The Plan: The cells should be ready at saturday for seeding and monday for transfection

We recived new HT1080 cells, they'll be split tomorrow (thx to Sven)

We recived new tumor cells which overexpress EGFR (thx to barbara)

Picking clones of pSB1C3_AAP_2, pSB1C3_AAP, pSB1C3_Rep78_2, pSB1C3_Rep78, pSB1C3_Rep68_2 and pSB1C3_Rep68

Investigator: Anissa
Of each construct two clones were picked. plates are still stored in the cold-room, tomorrow mini-prep will be done.

PCR and ligation for biobrick-production of pSB1C3_hTERT

Investigator: Anissa,Kerstin

Comments: PCR was performed one time without DMSO and one time with DMSO. Only the approach with DMSO showed bands in the analytic gel after PCR. That's why only this approach will be noted.

PCR:

(was performed following the standard protocol)

Ingredients	Volume / µl
5X Phusion HF buffer	10
10 mM dNTP mix	1
forward primer: O111 (phTERT_prefix_for_RFC10)	2,5
reverse primer: O112 (phTERT_suffix_rev_RFC10)	2,5
DNA Template	0,35 µl
DMSO (2%)	1
Phusion Polymerase	0,5
H₂O	32,15
Total volume	50

PCR program:

PCR Program	temperature/ °C
1	98
2	98
8x	58
3	72
4	98
17x	70
5	72
6x	72
Hold	4

BioBrick production of pSB1C3_hTERT
Preparative gel	analytic gel

Gel extraction

Gel measurement:

Sample	Weight	Volume	Concentration
hTERT	0,15g	20 µl	37,49 ng/µl
pSB1C3_cut	0,08g	20 µl	4,56 ng/µl

Digestion of PCR product and vector:

components	PCR product /µl	vector /µl
DNA	18	7,58
BSA (10x)	0,3 (100X used)	2
Buffer 4 (10x)	2,5	2
Enzyme XbaI	1	1
Enzyme PstI	1	1
H2O	2,2	6,42
Total volume (e.g. 15,20,25,30 µl)	25	20

Ligation with T4-Ligase and transformation with BL 21 was made. Clones have to be picked tomorrow.

Transformation evaluation of XL1B cells and repetition of transformation

Investigator: Kira
Against our expectations both agar plates contain very few colonies. In order to figure out if the lack of colonies is due to the XL1 blue cells or loss of pUC activity, test transformation will be repeated this evening with recently prepared XL1 blue cells as well as with Lab-XL1B cells. 50 pg pUC-plate contains 8 colonies 100 pg pUC-plate contains 18 colonies Transformation will be performed again with 100 pg pUC (= 2 ㎕ pUC).

Cloning of SDM SspI and SDM PvuII

Investigator: Chris W.

Vector: name: pSB1C3_SDM_SspI P125
Insert: name: pSB1C3_SDM_PvuII P129
new vector name: pSB1c3_SDM_SspI/PvuII P157
buffer used: 4 ; Restriction-enzymes used: Enzyme 1 (no. Lab: 144) BpmI ; Enzyme 2 (no.Lab: 152) ClaI
DNA concentration (vector): 321,9 ng/µl ; DNA concentration (insert): 308,4 µg/µl

components	volume of pSB1C3_SDM_SspI /µl	volume of pSB1C3_SDm_PvuII /µl
DNA	4,66	4,87
BSA (10x)	2	2
Buffer 4 (10x)	2	2
Enzyme BpmI (no.Lab:144)	1	1
Enzyme ClaI (no.Lab:152)	1	1
H2O	9,34	9,13
Total volume (e.g. 15,20,25,30 µl)	20	20

Comment: I guess enzyme 144 was BpmI and enzyme 152 was ClaI ? (Jessica)

Comment: u r right, changed (Chris)

0,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 130 Volt, running time:45

Loading plan for agarose gel:
Marker used: GeneRuler ladder mix (Fermentas)

	Marker	Sample 125, 20µl	Sample 129, 20µl
Lane	1	5	7

The mutual vector (now without SspI) and insert (now without PvuII) were cut out. The gelextraction was performed according to the standard protocol. DNA concentration of the extracts:

P125 Sspl: 12,8 ng/µl
P129 PvuII: 11,6 ng/µl

The Ligation was performed as following:

Vector Volume: 2,81 µl
Insert Volume: 5,19 µl

1µl T4-Ligase buffer (10x)
8µl (Vector + Insert) mix
1µl T4-Ligase

Incubate for 30min

Transformation: performed according to the standard protocol (BL21). The cells were plated on a agar plate with chloramphenicol

Miniprep of p158 and p159

Plasmid Mini-Prep

Investigator: Bea & Volker
For the tripple mutant of pAAV-RC a Quick-change reaction was carried out to remove the last restriction site (SalI) that is required for the Viral Brick standard. For this construct glycerol stocks and minipreps were carried out for two clones.

Glycerol Stocks

	Clone 1	Clone 2
Bacteria strain	BL-21	BL-21
Plasmidname	pAAV_RC_1.2 SDM SalI	align="left"\| pAAV_RC_1.2 SDM SalI
Date	05.08.2010	05.08.2010
given glycerol-stock no.	B126	B127
given plasmid no.	p158	p159

TO do: Test digestion and sequencing!!!

81.Labortag 06.08.2010

Cloning Rep40 & Rep52 into pSB1C3

Intention: get biobrick ready
Investigator: Patrick
PCR of pKEX-2XL.Rep 40 (P22) and pKEX-2XL.Rep 52 (P23) following gelrun (1%) and gelextraction.
Used Primers:

Praefix Rep40_52ex (O94)
Suffix Rep 40_68ex (O96)
Suffix Rep 52_78ex (O97)

PCR programm of Rep40:

98°C 1 min

98°C 15 sec
63°C 25 sec
72°C 15 sec Repeat this cycle 8 times.

98°C 15 sec
68°C 25 sec
72°C 15 sec Repeat this cycle 17 times.

72°C 5 min
Hold 4°C

PCR programm of Rep52:

98°C 1 min

98°C 15 sec
62°C 25 sec
72°C 20 sec Repeat this cycle 8 times.

98°C 15 sec
66°C 25 sec
72°C 20 sec Repeat this cycle 17 times.

72°C 5 min
Hold 4°C

ingredients	Rep 40	Rep40 + DMSO	Rep52	Rep52 + DMSO
5x Phusion HF buffer	10 µl	10 µl	10 µl	10 µl
10 mM dNTP mix	1 µl	1 µl	1 µl	1 µl
for Primer O94 (1:10 dilution, 05 µM)	2,5 µl	2,5 µl	2,5 µl	2,5 µl
rev Primer (1:10 dilution, 0,5 µM)	2,5 µl O96	2,5 µl O96	2,5 µl O97	2,5 µl O97
DNA template	1 µl, 112,7 ng/µl	1 µl, 112,7 ng/µl	0,9 µl, 142,3 ng/µl	0,9 µl, 142,3 ng/µl
DMSO	0 µl	0,5 µl	0 µl	0,5 µl
Phusion Polymerase	0,5 µl	0,5 µl	0,5 µl	0,5 µl
H2O	32,5 µl	32 µl	32,6 µl	32,1 µl
Total volume	50 µl	50 µl	50 µl	50 µl

Ecpected size of Rep40: 940 bp, expected size of Rep52:1198 bp. There are two samples of Rep40 and Rep52 and the PCR of one of each was run with 1% DMSO because the Rep40 Praefix has a strong secondary structure and was used as a primer for Rep 40 and Rep 52

Digestion of pSB1C3 (P51.1) with EcoRI-HF and SpeI following gelrun (0.8%) and gelextraction.
Expected size of the fragments: about 2000 bp and 800bp

All marked fragments were extracted. The Gelextraction was performed according to the standard protocol following a digestion of the PCR products with EcoRI HF and SpeI and a purification of the PCR product. The Ligation was not performed according to the standard protocol: 1 µl T4 DNA Ligase, 1 µl (10x) Buffer, 3 µl vector pSB1C3 (60 ng/µl) and 5 µl insert (all concentrations about 100 ng/µl). The Transformation (with BL21) was performed according to the standard protocol. Tomorrow there will hopefully be some clones on the agar plates.

BioBrick Assembly of pSB1C3_beta globin_mVenus

Investigator: Bea

Comments: BioBricks are ready to use. The sequenced pSB1C3_beta globin (P133) and pGA14_mVenus (P60) will be digested with different enzymes and will be assembled in order to produce the first step in assembling the whole vector together.

First the plasmids P133 and P60 were digested:

	pSB1C3_betaglobin/µL	pGA14_mVenus/µL
DNA	7	9
BSA (100x)	0,2	0,2
Buffer 4 (10x)	2	2
Enzyme XbaI	1	1
Enzyme AgeI	1	1
H2O	8,8	6,8
Total volume	20	20

Incubation of plasmids at 37°C for 2 hours
Load samples on preparative 1% agarose gel and run at 110 V, 45 minutes

Results: As it can be seen in the picture below, digestion of the vector pSB1C3_betaglobin (left lane) revealed a band at around 2500 - 3000 bp. The expected size after digetsing with SpeI and PstI was: 2555 bp. The band ran a little bit higher than expected, anyhow the band was cut out of the gel. The right lane belongs to the pGA14_mVenus which was digested with XbaI and PstI which resulted in two fragments. mVENUS was digested. Expected sizes were: mVenus = 756bp and pGA14 = 2900bp. The expected sizes correspond to the bands seen in the picture below. The smaller fragment belonging to mVenus was cut out of the gel as well.

After gel extraction has been performed, the concentrations of the two fragments were measured and we obtained following concentrations:

c(pSB1C3_betaglobin) = 15,62 ng/µL
c(mVenus) = 6,83 ng/µL

For ligation the T4-Ligase were used.

v(pSB1C3_betaglobin) = 2,64 µL
v(mVenus) =5,36 µL
v(10xT4 Ligase buffer) = 1 µL
v(T4-Ligase) = 1 µL
Total volume = 10 µL

Additionally a control ligation was performed.

v(pSB1C3_betaglobin) = 2,64 µL
v(H₂0) =5,36 µL
v(10xT4 Ligase buffer) = 1 µL
v(T4-Ligase) = 1 µL
Total volume = 10 µL
Ligation duration was 45 minutes on room temperature.

After ligation a transformation was performed.

Used bacterial strain: XL1-B
LB-agar plates containing chloramphenicol were plated and put in the 37°C room over night

To do: Mini-Prep and test digestion in order to verify assembly of beta globin and YFP. After verification of the fusion of the two fragments this construct is ready for the next BioBrick assembly step.

Test digestion of SalI SDM

Investigator: Hanna

Test digestion

buffer used: 3 ; Restriction-enzymes used: Enzyme 1 (no. Lab: 53): SalI ; Enzyme 2: XbaI
Plasmid
- Given Plasmid-Number: P158; DNA concentration: 398.8 ng/µL ;
- Given Plasmid-Number: P159; DNA concentration: 437.4 ng/µL ;

Components	P158 Volume/µL	P159 Volume/µL
DNA	2.5	2.3
BSA (10x)	1	1
Buffer 3 (10x)	1	1
SalI (no. Lab: 53)	0.5	0.5
XbaI	0.75	0.75
H₂O	4.25	4.45
Total volume	10	10

Incubation: 1 h

Agarose-Gel:

0.5 g Agarose, 50 mL TBE (1 %),3 µL GELRED, at 115 Volt, running time: 45 minutes

Sample	Sample/µl]	Loading dye (5x)/µl	Expected size 1 (if SDM didn't work)	Expected size 2 (if SDM didn't work)	Expected size 3 (if SDM didn't work)
P158	10 µl	2 µl	6129 bp	1143 bp	61 bp
P159	10 µl	2 µl	6129 bp	1143 bp	61 bp

Marker: GeneRuler ladder mix

	Marker /µL	Sample P158 /µl	Sample P159 /µl	Marker /µL
Lane	6.5	10	10	7

Comments: Test digestion looked good: No 1143 bp fragment was detectable in neither test digestion.
P158 was sent for sequencing to GATC.

ITR test digestion of pAAV_MCS

Investigator: Hanna

Comment: Because sequencing of the right ITR delivered that perhaps a 15 bp fragment is missing in the sequence, we wanted to check, whether this fragment is also not present in the original pAAV_MCS plasmid or whether the loss of these 15 bp happened during cloning.

Test digestion

buffer used: 4 ; Restriction-enzymes used: Enzyme 1: NotI; Enzyme 2: PstI
Plasmid
- Plasmid-Number: from Sven; DNA concentration: 259 ng/µL ;

Components	Volume/µL
DNA	3.8
BSA (10x)	1.5
Buffer 4 (10x)	1.5
NotI-HF	0.75
PstI-HF	0.75
H₂O	3.2
Total volume	15

Incubation: 1 h

Agarose-Gel:

0.5 g Agarose, 50 mL TBE (1 %),3 µL GELRED, at 115 Volt, running time: 45 minutes

Sample	Sample/µl]	Loading dye (5x)/µl	Expected size ITRs	Expected size 2	Expected size 3	Expected size 4
pAAV_MCS	15 µl	2 µl	145 bp	1216 bp	555 bp	2608 bp

Marker: GeneRuler ladder mix

	Marker /µL	Sample /µl	Marker /µL
Lane	6.5	12	6.5

Comments: The test digestion showed that there're two bands between the 100 and 200 bp marker nucleotides! By comparing the gel picture with the last mini-prep digestion of the fancy method we found out that the space between the two bands are similar. Because of that we assumed that the 15 pb are already missing in the original Stratagene plasmid!!!

Conclusion: Because we already tested the Stratagene Kit via YFP expression, we can conclude that the usage of the "wrong" rigth ITR works. Therefore we decided to continue working with this "mutated" = ENGINEERED :) right ITR as BioBrick.

Miniprep of pSBC13_Rep78, pSB1C3_Rep68, pSB1C3_AAP, pSB1C3_rightITR and psB1C3_leftITR

Plasmid Mini-Prep

Investigator: Kerstin

Glycerol Stocks
pSB1C3_Rep78

	Clone 1	Clone 2
Bacteria strain	BL-21	BL-21
given glycerol-stock no.	B128	B129
given plasmid no.	P160	p161
DNA-concentration ng/µl	139,1	71,0

pSB1C3_2_Rep78

	Clone 1	Clone 2
Bacteria strain	BL-21	BL-21
given glycerol-stock no.	B130	B131
given plasmid no.	P162	p163
DNA-concentration ng/µl	112,1	79,7

pSB1C3_Rep68

	Clone 1	Clone 2
Bacteria strain	BL-21	BL-21
given glycerol-stock no.	B132	B133
given plasmid no.	P164	p165
DNA-concentration ng/µl	80,2	72,8

pSB1C3_2_Rep68

	Clone 1	Clone 2
Bacteria strain	BL-21	BL-21
given glycerol-stock no.	B134	B135
given plasmid no.	P166	p167
DNA-concentration ng/µl	85,6	69,1

pSB1C3_AAP

	Clone 1	Clone 2
Bacteria strain	BL-21	BL-21
given glycerol-stock no.	B136	B137
given plasmid no.	P168	p169
DNA-concentration ng/µl	63,6	56,3

pSB1C3_2_AAP

	Clone 1	Clone 2
Bacteria strain	BL-21	BL-21
given glycerol-stock no.	B138	B139
given plasmid no.	P170	p171
DNA-concentration ng/µl	135,1	114,2

pSB1C3_rightITR

	Clone 1	Clone 2
Bacteria strain	BL-21	BL-21
given glycerol-stock no.	B140	B141
given plasmid no.	P172	p173
DNA-concentration ng/µl	73,7	66,4

pSB1C3_leftITR

	Clone 1	Clone 2
Bacteria strain	BL-21	BL-21
given glycerol-stock no.	B142	B143
given plasmid no.	P174	p175
DNA-concentration ng/µl	74,9	80,3

Test digestion:
pSB1C3_Rep78, pSB1C3_Rep68 and pSB1C3_AAP were digested with XbaI and SpeI
pSB1C3_rightITR and pSB1C3_leftITR were digested with EcoRI and PstI.

components	volume of P160/µl	volume of P161/µl	volume of P162/µl	volume of P163/µl	volume of P164/µl	volume of P165/µl	volume of P166µl	volume of P167/µl	volume of P168µl	volume of P169/µl	volume of P170/µl	volume of P171/µl	volume of P172/µl	volume of P173µl	volume of P174/µl	volume of P175/µl
DNA	5,8	11,3	7,1	10	9,9	10,9	9,3	11,6	12,5	14,2	5,9	7,0	10,9	12,0	10,7	9,7
BSA (10x)	2	2	2	2	2	2	2	2	2	2	2	2	2	2	2	2
Buffer 4 (10x)	2	2	2	2	2	2	2	2	2	2	2	2	2	2	2	2
Enzyme 1	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5
Enzyme 2	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5
H2O	9,2	3,7	7,9	5,0	5,1	4,1	5,7	3,4	2,5	0,8	9,1	8	4,1	3	4,3	5,3
Total volume /µl	20	20	20	20	20	20	20	20	20	20	20	20	20	20	20	20

Expected sizes:

Rep78: 1,8 kb
Rep68: 1,6kb
AAP: 650bp

left ITR: 150bp
right ITR: 150bp

Results of samples loaded 1,5% agarose gel and ran ~50 minutes at 115 V:

Results of samples loaded 0,8% agarose gel and ran ~50 minutes at 115 V:

Sequencing

P160, P165 and P170 were send for sequencing.

82.Labortag 07.08.2010

Cellculture

HEK 293 cells were split and seeded according to the standard protocol: 2x T75 flask and 10x10cm cellculture dishes. Investigator: Patrick

Continuation: Cloning Rep40 & Rep52 into pSB1C3

Investigator: Patrick
Results: no clones could be picked because there were no clones. Maybe the PCR purification or one of the following steps did not work (the PCR purifications were quite bad) so i purified the PCR products again yielding very low DNA concentrations (0-13,28 ng/µl) and still very obvious pollution of the sample. Nonetheless a ligation with the insert Rep40+DMSO, Rep52, Rep52+DMSO and the vector pSB1C3 was carried out following a transformation and according to the standard protocols. Hopefully there will be some clones tomorrow.

Mini-Prep and test digestion of pSB1C3_SDM_SspI/PvuII

Investigator: Jessica

Plasmid Mini-Prep

new vector name: pSB1C3_SDM_SspI/PvuII

Glycerol Stocks
pSB1C3_SDM_SspI/PvuII

	Clone 1	Clone 2	Clone 3
Bacteria strain	BL21	BL21	BL21
Plasmidname	pSb1C3_SDM_SspI/PvuII	pSb1C3_SDM_SspI/PvuII	pSb1C3_SDM_SspI/PvuII
Date	7.8.10	7.8.10	7.8.10
given glycerol-stock no.	B144	B145	B146
given plasmid no.	P157.1	P157.2	P157.3

Test digestion

buffer used: 2 ; Restriction-enzymes used: Enzyme 1 SspI ; Enzyme 2 PvuII
Plasmid: pSB1C3_SDM_SspI/PvuII:
- Given Plasmid-Number: P157.1; DNA concentration: 246,3 ng/µL ;
- Given Plasmid-Number: P157.2; DNA concentration: 231,7 ng/µL ;
- Given Plasmid-Number: P157.3; DNA concentration: 219,6 ng/µL ;

Components	P157.1 Volume/µL	P157.2 Volume/µL	P157.3 Volume/µL
DNA	2,8	3,0	3,19
BSA (10x)	-	-	-
Buffer no. 2 (10x)	1	1	1
Enzyme 1 SspI	0.5	0.5	0.5
Enzyme 2 PvuII	0.5	0.5	0.5
H₂O	5,2	5	4,81
Total volume	10	10	10

Incubation: 45 min

Agarose-Gel:

0.45 g Agarose, 50 mL TAE, 3 µL GELRED, at 115 Volt, running time: 45 minutes

Sample	Sample/µl]	Loading dye (6x)/µl
P157.1	10 µl	1,6 µl
P157.2	10 µl	1,6 µl
P157.3	10 µl	1,6 µl

Marker: GeneRuler ladder mix

	Marker /µL	Sample P157.1 /µL	Sample P157.2 /µL	Sample P157.3 /µL
Lane	7	10	10	10

I expect one cut from the PvuII RS in the CFP --> linearized

Comment:

Comments:Oh f... it makes no sense... if the cloning didn't work, there can just be 3 bands (one time SspI and twice PvuII). The results of the test digestion from aug 1th showed that there can be one RS PvuII more. but then you have a maximum of 4 bands. P157.2 show 5 bands. i can't interpret this result at the moment. interpretation will follow

Evaluation of test transformation with XL1 blue cells and pUCI

Investigator: Kira

Transformation was performed with lab XL1B and iGEM XL1B cells. iGEM plate contained just 25 colonies, while lab plate contained around 50 colonies. Conclusion: the production of competent cells has to be repeated.

Biobrick production of p5 promoter from pTAV2 and pAAV_RC

Investigator: Kira

PCR:

DNA samples were diluted 1:100

Ingredients	p 32	p 50
5X Phusion HF buffer	10 µl	10 µl
10 mM dNTP mix	1µl	1 µl
forward primer: O114	2,5µl	2,5 µl
reverse primer: O115	2,5 µl	2,5 µl
DNA Template	0,3 µl	0,4 µl
DMSO	0 µl	0 µl
Phusion Polymerase	0,5 µl	0,5 µl
H₂O	33,2 µl	28,6 µl
Total volume	50 µl	50 µl

PCR program:

Cycles	Temperature	Time
	98°C	1
8x	98°C	30"
	60°C	25"
	72°C	6"
17x	98°C	30"
	70°C	25"
	72°C	6"
1x	72°C	5'
Hold 4°C

Digestion of plasmid backbone:

c (pSB1C3) = 151, 1 ng/ µl

Components	vector Volume/µL
DNA 1 µg	6,0 µl
BSA (100x)	0,2 µl
Buffer no. 4 (10x)	2,0 µl
Enzyme 1 XbaI	1 µl
Enzyme 2 PstI HF	1 µl
H₂O	9,8 µl
Total volume	20

incubation @ 37 C for approx. 2 h

1% agarose gel with PCR products:

Concentrations after gel extraction:

c(p32) = 67,95 ng/µl
c(p50) = 32,45 ng/µl
c(vector) = 7,54 ng/µl

Digestion of PCR products:

Components	PCR product Volume/µL
DNA 1 µg	23,0 µl
BSA (100x)	0,3 µl
Buffer no. 4 (10x)	3,0 µl
Enzyme 1 XbaI	1,5 µl
Enzyme 2 PstI HF	1,5 µl
H₂O	0,7 µl
Total volume	30

Concentrations after PCR purification:

c(p32) = 21, 63 ng/µl
c(p50) = 19,48 ng/µl

Ligation:

Quickligase was used for ligation.

p32 DNA-Mix: 8 µl vector + 1 µl insert
p50 DNA-Mix: 7,9 µl vector + 1,1 µl insert

Transformation:

Transformation was performed according to the standard protocol with DYT and BL21 cells. The cells were spread on the agar plates containing chloramphenicol.

Sequencing results of SalI SDM

Investigator: Hanna

Comment: The test digestion already showed that the SDM of the SalI restriction site in pAAV_RC worked. This could be validated by sequencing the plasmid with the Rep-1250_for primer:

P58 can be used for further RepCap-experiments.

83. Labortag 08.08.2010

HT 1080 cells were split and seeded: 3x10^6 cells per into each well of a 6-well plate.

A431 cells were washed and received new medium.

There were no clones on the agar plates so they were put back into the 37°C room. Maybe there will be some clones tomorrow.

84. Labortag 09.08.2010

Midi-Prep Inoculation

pAAV_RC
pAAV_RC_1.2 SDM SalI (P158)
pAAV_RC_mGMK_TK30 clone 1 (P81)
pAAV_RC_mGMK_TK30 clone 2 (P82)

Investigators: Chris W., Patrick

Continuation: Cloning Rep40 & Rep52 into pSB1C3

Investigator: Patrick
Two Rep52+DMSO clones grew. They were picked and tomorrow there will be a midi prep and a test digestion. Simultaneously a new approach for cloning Rep40 and Rep52 into pSB1C3 was performed. (see next header)

Repetition: BioBrick production of Rep40 & Rep52

Investigator: Anna

Comments: Another approach was done because there were no clones for Rep 40 and only two for Rep 52 (Cloning see 06.08.2010). PCR was performed again with DMSO. Samples from gel extraction are stored in 4°C freezer.

PCR

Ingredients	Rep 40	Rep52
5X Phusion HF buffer	10 µl	10 µl
10 mM dNTP mix	1µl	1 µl
forward primer: O094	2,5µl	2,5 µl
reverse primer: O0096/ O097	2,5 µl	2,5 µl
DNA Template (1ng)	1 µl	1 µl
DMSO	1 µl	1 µl
Phusion Polymerase	0,5 µl	0,5 µl
H₂O	31,5 µl	31,5 µl
Total volume	50 µl	50 µl

PCR programm

PCR Program	temperature/ °C	Time	PCR products
1	98	1min
2	98	15s
8x	***	15s	63°C
3	72	***	15s
4	98	15s
19x	***	15s	68°C
5	72	***	15s
6x	72	5min
Hold	4

Agarose gel

0.5 g Agarose, 50 mL TAE (1 %),3 µL GELRED, at 120 Volt, running time: 45 minutes

Sample	Sample / µl]	Loading dye (6x) / µl	Expected size
p22 (Rep40)	44 µl	7 µl	940 bp
p23 (Rep52)	44 µl	7 µl	~1200 bp

Marker: GeneRuler ladder mix

	Marker /µL	Sample Rep40 /µl	Sample Rep52 /µl
Lane	7	51	51

Gel extraction
PCR products were eluted with 20 µl BE puffer following the standard protocol.
c(Rep40)= 28,03 ng/µl
c(Rep52)= 121,16 ng/µl

Comments: Digestion was done with the wrong enzymes (EcoRI HF and SpeI), it will be repeated on 11.08. with XbaI and SpeI

Sequence analysis of pSB1C3_mGMK

Investigator: Bea

Comments: mGMK was cloned into the pSB1C3 backbone in order to send it to the parts registry!. The sequence analysis revealed that the mGMK was successfully cloned into pSB1C3 plasmid. This polasmid is in the RFC25 standard.

Results sequencing: Sequence read ok!

Mini-Prep of pSB1C3_hTERT, pSB1C3_beta-globin_mVenus, pSB1C3_pTAV2(P5), pSB1C3_pAAV_RC(P5TATAles)

Investigator: Jessica

Bold text Mini-Prep following the standart Protokoll

P177 = pSB1C3_hTERT clone1 = 163,6 ng/µl

P178 = pSB1C3_hTERT clone2 = 312,0 ng/µl

P179 = pSB1C3_betaglobin_mVenus clone1 = 237,2 ng/µl

P180 = pSB1C3_betaglobin_mVenus clone2 = 228,2 ng/µl

P181 = pSB1C3_pTAV2(P5) clone1 = 108,8ng/µl

P181 = pSB1C3_pTAV2(P5) clone2 = 140,9 ng/µl

P181 = pSB1C3_pAAV_RC(P5TATAless) clone1 = 165,0 ng/µl

P181 = pSB1C3_pAAV_RC(P5TATAless) clone2 = 176,6 ng/µl

P181 = pSB1C3_pAAV_RC(P5TATAless) clone3 = 176,9 ng/µl

Test digestion:

Perfomed with 10 µL of total volume with all 9 clones

	Mastermix/µL	P176/µL	P177/µL	P178/µL	P179/µL	P180/µL	P181/µL	P182/µL	P183/µL	P184/µL
DNA	-	4,3	2,3	3,0	2,4	6,4	5,0	4,2	4,0	4,0
BSA (10x)	10	3	3	3	3	3	3	3	3	3
Buffer 4 (10x)	10
Enzyme XbaI	5
Enzyme AgeI	5
H2O	-	2,7	4,7	4,0	4,6	0,6	2,0	2,8	3,0	3,0
Total volume	30	10	10	10	10	10	10	10	10	10

All 9 samples were loaded on a 1% agarose gel
P176 = pSB1C3_hTERT clone1
P177 = pSB1C3_hTERT clone2
P178 = pSB1C3_betaglobin clone1
P179 = pSB1C3_betaglobin clone2
P180 = pSB1C3_pTAV2(P5) clone1
P181 = pSB1C3_pTAV2(P5) clone2
P182 = pSB1C3_pAAV_RC(P5TATAless) clone1
P183 = pSB1C3_pAAV_RC(P5TATAless) clone2
P184 = pSB1C3_pAAV_RC(P5TATAless) clone3

Sample	Sample/µl]	Loading dye (6x)/µl	Expected size 1 (Geneious)
P176	10 µl	1,6 µl	474 bp
P177	10 µl	1,6 µl	474 bp
P178	10 µl	1,6 µl	509 bp
P179	10 µl	1,6 µl	509 bp
P1780	10 µl	1,6 µl	164 bp
P181	10 µl	1,6 µl	164 bp
P182	10 µl	1,6 µl	164 bp
P183	10 µl	1,6 µl	164 bp
P184	10 µl	1,6 µl	164 bp

Comments: hTERT and betaglobin_mVenus is inserted in pSB1C3, pTAV(P5) and pAAV_RC (P5TATAless) will be sequenced

Primer: Reverse Primer VR2

Cell culture

Investigators: Adrian, Kerstin, Patrick

Transfection on HEK293

The motivation: first we want to create new stock of AAV without GOI, the next viral stock is with correct TK/GMK, the last stocks are with different YFP-amounts to check if the amount of GOI is a critical step for transduction effency (transgene expression).

Plate	pAAV_RC/µg	pHelper/µg	GOI/µg
1	3,3	3,3	no GOI
2	6,6	3,3	no GOI
3	3,3	3,3	3,3 TK_GMK clone1
4	3,3	3,3	3,3 TK_GMK clone1
5	3,3	3,3	3,3 TK_GMK clone2
6	3,3	3,3	3,3 YFP
7	3,3	3,3	10 YFP
8	3,3	3,3	20 YFP
9	3,3	3,3	40 YFP
10	3,3	3,3	60 YFP

Transduction of HT1080

Motivation The Motivation: checking survivalrate of Cells, with either no Virus, virus without GOI and virus with YFP (10µg stock)
The Plan:
Plate I

control, no cells	no GOI 150µl	10µg 500µl\|
control, no virus	no GOI 300µl	10µg 750µl\|

Plate II

control, no cells	no GOI 150µl	10µg 500µl\|
control, no virus	no GOI 300µl	10µg 750µl\|

Plate III

control, no cells	no GOI 150µl	10µg 500µl\|
control, no virus	no virus	10µg 750µl\|

Passaging and seeding of A431

one 6er dish was prepared for making pictures and one T75 Flask.

BioBrick Assembly of pSB1C3_leftITR_CMV and pSB1C3_hGH_rightITR

Investigator: Bea, Achim, Jo

Comments: In order to proceed with the BioBrick assembly the pasmids pSB1C3_left ITR and pSB1C3_CMV were used and pSB1C3_rigthITR and pSB1C3_hGH were used in order to obatin plasmids with both sequences.

BioBrick assembly of pSB1C3_hGH_rightITR and pSB1C3_leftITR_CMV
Cloning strategy of pSB1C3_leftITR CMV	pSB1C3_hGH_rightITR

Digestion:

components	pSB1C3_left ITR	pSB1C3_CMV	pSB1C3_right ITR	pSB1C3_hGH
DNA	13,4	9,5	13,6	6,6
BSA (10x)	2	2	2	2
Buffer 4 (10x)	2	2	2	2
Enzyme1	1 (SpeI)	1 (Xba1)	1 (EcoRI)	1 (EcoRI)
Enzyme2	1 (PstI)	1 (PstI)	1 (XbaI)	1 (SpeI)
H2O	0,6	4,5	0,4	7,4
Total volume	20	20	20	20

Preparation of gel:
0,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 115 Volt, running time: 45 minutes

Oh, nice picture.. I can recognize many details :)*g* (Hanna)

Expected sizes of constructs:

pSB1C3_CMV: 650 bp
pSB1C3_lITR: 2200 bp
pSB1C3_hGH: 500 bp
pSB1C3_rITR: 2200 bp

The correspnding bands were cut out and Gel-Extraction was performed according to protocol.

concentrations measured via NanoDrop:

pSB1C3_CMV: 13,51 ng/µl
pSB1C3_lITR: 18,49 ng/µl
pSB1C3_hGH: 7,22 ng/µl
pSB1C3_rITR: 20,24 ng/µl

Ligation:
For ligation, T4 ligase was used.

1µl T4-Ligase buffer (10x)
8µl (Vector + Insert) mix
1µl T4-Ligase

Ligation was carried out as following:

Ligation 1:
- pSB1C3_CMV: 4,4 ng/µl
- pSB1C3_lITR: 3,6 ng/µl
Ligation 2:
- pSB1C3_hGH: 5,25 µl
- pSB1C3_rITR: 2,75 µl

Incubation for 40 minutes.

Transformation:
Transformation carried out according to standard protocol (BL21). Cells were plated on an agar plate with chloramphenicol.

Repetition: Cloning of SDM SspI and SDM PvuII

Investigator: Stefan

Comments: Last week's cloning of SDM_SspI and SDM_PvuII didn't work out, so this is the repetition. In this approach the same restriction enzymes and amounts of DNA were used.

Vector: name: pSB1C3_SDM_SspI P125
Insert: name: pSB1C3_SDM_PvuII P129

buffer used: 4
Restriction-enzymes used:
- BpmI (no. Lab: 144)
- ClaI (no.Lab: 152)
DNA concentration (P125): 321,9 ng/µl
DNA concentration (P129): 308,4 ng/µl

Digestion:

components	volume of pSB1C3_SDM_SspI /µl	volume of pSB1C3_SDm_PvuII /µl
DNA	4,66	4,87
BSA (10x)	2	2
Buffer 4 (10x)	2	2
BpmI (no.Lab:144)	1	1
ClaI (no.Lab:152)	1	1
H2O	9,34	9,13
Total volume	20	20

Gel extraction:
Preparation of gel:
0,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 115 Volt, running time: 45 minutes

Expected sizes of constructs:

pSB1C3_SDM_SspI: 1819 bp
pSB1C3_SDM_PvuII: 981 bp

The correspnding bands were cut out and Gel-Extraction was performed according to protocol.

Freiburg10 pSB1C3 SDM SspI and PvuII 090810.png

concentrations measured via NanoDrop:

Sspl: 19,85 ng/µl
PvuII: 10,57 ng/µl

Ligation:
For ligation, T4 ligase was used.

1µl T4-Ligase buffer (10x)
8µl (Vector + Insert) mix
1µl T4-Ligase

The Ligation was performed as following:

SDM_SspI Volume: 4,03 µl
SDM_PvuII Volume: 3,97 µl

1µl T4-Ligase buffer (10x)
8µl (Vector + Insert) mix
1µl T4-Ligase

Incubating for 45 minutes.

Transformation:
Transformation performed according to the standard protocol (BL21). The cells were plated on a agar plate with chloramphenicol.

Design and ordering of primer for P40 Promoter BioBrick production

Investigator: Hanna

In order to generate a P40 promoter BioBrick = "Cap-Promoter", oligos were designed and ordered at Sigma Aldrich:

85. labday 10.08.2010

Retrafo with RepCap gene (Mr.Gene)

Investigator: Bea

Comments: We received the rep_cap insert ordered from Mr. Gene today. In order to used and clone the insert into the desired sequences a retrafo has to be performed.

Re-transformation:

Construct used: pMA_REP_CAP
We reveived 5 µg (lyophilzied). These were resuspended in 100 µL H₂O and vortexted.
c = 50 ng/µL
c = Plasmid need to be diluted in order to obatain the final 500pg
Dilution: 1:100
100 µL aliquot of XL1-B were thawed on ice. The proper amount of 1µL was added to the cells.
Transformed cells were plated on LB plates containing ampicillin

Continuation: Cloning Rep40 & Rep52 into pSB1C3

A midi prep of the two Rep52+DMSO clones was performed yielding concentrations of 261,35 ng/µl (clone 1) and 240,47 ng/µl (clone 2). Unfortunately we noticed today that we should not use EcoRI to clone Rep52 into pSB1C3 because EcoRI cuts two times within the sequence of Rep52.

Midi-Prep of pAAV_RC, pAAV_RC_1.2 SDM SalI (P158), pAAV_RFC25_mGMK_TK30 clone 1 (P81) and 2 (P82)

Investigators: Patrick, Chris

The Midi-Preps were performed according to the standard protocol yielding the following concentrations:

pAAV_RC	P81a	P81b	P82a	P82b	P158a	P158b
1348,49 ng/µl	1783,86 ng/µl	2096,25 ng/µl	1915 ng/µl	1469,35 ng/µl	1834,25 ng/µl	1771,27 ng/µl

The annotations a and b were added because two midi-preps of P81, P82 and P158 were carried out.

Results of sequencing pSB1C3_pTAV2(P5) and Psb1C3_pAAV_RC(P5TATAless)

Investigator: Jessica

@Jessi: Which clones are ok, which not?? text does not correspond to pictures! (Bea)

Freiburg10 Sequence alignment P5 mit TATA clone1neu.jpg

sequencing of P180 was successful, P5 with TATAbox is in pSB1C3

Freiburg10 Sequence alignment P5TATAless clone2neu.jpg

sequencing of P183 was successful but there is a G missing --> plamid is thrown away

Freiburg10 Sequence alignment P5TATAless clone3.jpg

sequencing of P184 was successful, P5 is in without TATAbox. this plasmid can be used.

P181 and P180 are thrown away because of the result of the test digestion.

Repetition: BioBrick production of Rep40 and Rep 52

Investigator: Anna

Comments: PCR was repeated once again (that was bad!), because digestion was done with the wrong enzymes (EcoRI HF and SpeI). There are some differences in the PCR programm in comparison to the last (see 09.10.)

PCR

Ingredients	Rep 40	Rep52
5X Phusion HF buffer	10 µl	10 µl
10 mM dNTP mix	1µl	1 µl
forward primer: O094	2,5µl	2,5 µl
reverse primer: O0096/ O097	2,5 µl	2,5 µl
DNA Template 1:100 (1ng)	1 µl	1 µl
DMSO	1 µl	1 µl
Phusion Polymerase	0,5 µl	0,5 µl
H₂O	31,5 µl	31,5 µl
Total volume	50 µl	50 µl

PCR programm

PCR Program	temperature/ °C	Time	PCR products
1	98	1min
2	98	15s
8x	***	15s	62,5°C
3	72	***	25s
4	98	15s
19x	***	15s	67°C
5	72	***	25s
6x	72	5min
Hold	4

Agarose gel

0.5 g Agarose, 50 mL TAE (1 %),3 µL GELRED, at 120 Volt, running time: 45 minutes

Sample	Sample / µl]	Loading dye (6x) / µl	Expected size
p22 (Rep40)	50 µl	8 µl	940 bp
p23 (Rep52)	50 µl	8 µl	~1200 bp

Marker: GeneRuler ladder mix

	Marker /µL	Sample Rep40 /µl	Sample Rep52 /µl
Lane	7	58	58

Comments: Digestion of the samples will be done tomorrow with XbaI and SpeI.

Gelextraction

Elution was done with 20 µl Pe buffer following the standard protocol.

c(Rep40)= 23,1 ng/µl
c(Rep52)= 78,0 ng/µl

Preparation of competent XL1blue and testtrafo

Investigator: Jessica
preparation of competent E.coli XL1blue was made according to the standardprotocol (91 eppis with 60µl) they are in the green boxes in -80°C
testtrafo was made

one plate with 50pg/µl
one plate with 100pg/µl

...trafo is failed because amp was missing on the plates (resistence in pUC). trafo will be repeated on aug 11th by Tobi...

Repetition: Mini-Prep and test digestion of pSB1C3_SDM_SspI/PvuII

Investigator: Adrian, Stefan

Plasmid Mini-Prep

vector name: pSB1C3_SDM_SspI/PvuII

Glycerol Stocks
pSB1C3_SDM_SspI/PvuII Only clone 1 grew, therefore there is just one stock = B159

Test digestion

buffer used: 2
Restriction-enzymes used:
- Enzyme 1 SspI
- Enzyme 2 PvuII
Plasmid: pSB1C3_SDM_SspI/PvuII:
- Plasmid-Number: P185; DNA concentration: 47,9 ng/µL

comment: DNA was eluted into previously used tube, therefore contamination is possible.

Components	P185 Volume/µL	P51.1 Volume/µL
DNA	18,1	6,8
BSA (10x)	2,5	2,5
Buffer no. 2 (10x)	2,5	2,5
Enzyme 1 SspI	0.5	0.5
Enzyme 2 PvuII	0.5	0.5
H₂O	0,9	12,2
Total volume	10	10 \|

Incubation: 45 min

Agarose-Gel:

0.4 g Agarose, 50 mL TAE, 3 µL GELRED, at 115 Volt, running time: 45 minutes

Marker: GeneRuler ladder mix

	Marker /µL	Sample P185 /µL	Sample P51.1 /µL
Lane	7	17	17

One cut is expected (PvuII in CFP).

Comment: There are 6 bands now. This test digestion again looks very different from that of P157.2 done by Jessica (lab day 82). Results should be discussed tomorrow.

Picking clones of pSB1C3_SDM_SspI/PvuII

Investigator: Stefan

Comments: Test digestion didn't work out, three additional clones were picked from the plate we get from yesterday's Trafo to retry tomorrow.

Bacterial strain used: BL21
Inoculating of 10 mL DYT medium containing 10µL chloramphenicol
Put in 37°C room on shaker at 20.45hours.

86. labday 11.08.2010

Biobrick Assembly:Picking Clones, Miniprep, Testdigestion of CMV&lITR/ hGH & rITR

Investigator: Chris L., Achim Test Digestion showed that the cloning was succesful.

NanoDrop concentrations:

hGH_rITR1:105,15 ng/µl
hGH_rITR2:96.97 ng/µl
CMV_lITR1:231.61 ng/µl
CMV_lITR2:129.19 ng/µl

Biobrick Assembly: bSB1C3_lITR_CMV & pSB1C3_betaglobin_mVenus

Investigator: Chris L., Achim

Comments: In order to proceed with the BioBrick assembly the plasmids pSB1C3_leftITR_CMV was cut with SpeI and PstI, pSB1C3_betaglobin_mVenus was cut with XbaI and PstI. The insert fragment containing betaglobin_mVenus was ligated to the vector fragment containing the leftITR_CMV promotor.

Digestion:

components	pSB1C3_leftITR_CMV	pSB1C3_betaglobin_mVenus
DNA	5,2	8,4
BSA (10x)	2	2
Buffer 4 (10x)	2	2
Enzyme1	1 (SpeI)	1 (Xba1)
Enzyme2	1 (PstI)	1 (PstI)
H2O	8,8	5,6
Total volume	20	20

Preparation of gel:
0,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 115 Volt, running time: 45 minutes

Expected sizes of constructs:

pSB1C3_leftITR_CMV: 2800 bp
pSB1C3_betaglobin_mVenus: 1200 bp, 2000 bp

The corresponding bands were cut out and Gel-Extraction was performed according to protocol.

concentrations measured via NanoDrop:

pSB1C3_leftITR_CMV: 55,5 ng/µl
pSB1C3_betaglobin_mVenus:: 10,4 ng/µl

Continuation of Cloning of Rep40/52

Investigator: Anna

Digestion of PCR products and vector:

components	PCR product /µl	vector /µl
DNA	19	10
BSA (10x)	3	3
Buffer 4 (10x)	3	3
Enzyme XbaI	1	1
Enzyme SpeI	1	1
H2O	3	12
Total volume (e.g. 15,20,25,30 µl)	30	30

Comments: This time digestion was done with XbaI and SpeI (means it has to be checked if the inserts are cloned into the vector in the right orientation).

Purification of Rep40 and Rep52:

For the purification 95 µl of buffer PBI was used.

c(Rep40)= 12,5 ng/µl
c(Rep52)= 51,8 ng/µl

Gelextraction of pSB1C3_RFC25_CFP:

0,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 120 Volt, running time:55
5µl loading dye (6x) for the sample, Marker: GeneRuler ladder mix (Fermentas)

c(pSB1C3)= 10,59 ng/µl
c(pSB1C3_2)= 4,25 ng/µl

Ligation of PCR products and vector:

For the Ligation 1µl T4 buffer (2x) and 1µl T4 ligase were used.

	Sample-no.	vector /µl	insert /µl
pSB1C3 + Rep40	1	3,65	4,35
pSB1C3 + Rep52	2	5,87	2,13
Total volume (e.g. 15,20,25,30 µl)	8

Transformation:

The transformation was done following the standard protocol using B21 cells.

PCR of bla_14FM and ligation into pSB1C3_SDM_SspI and pSB1C3_SDM_PvuII for virobrick-production T

Investigator: Anissa,Kerstin

Comments: Because it still is unclear if SDM of pSB1C3_SspI_PvuII has worked, we decided to use the one time mutagenisised vector pSB1C3_SDM_SspI, to clone bla into it and to make the second mutation of PvuII after bla is inserted. .

PCR:

(was performed following the standard protocol)

Ingredients	v(pTB106_bla14FM) - DMSO / µl	v(pTB106_bla14FM) + DMSO / µl
5X Phusion HF buffer	10	10
10 mM dNTP mix	1	1
forward primer: O116(P extreme f)	2,5	2,5
reverse primer: O117 (P extreme r)	2,5	2,5
DNA Template 1ng	5,3 µl	5,3 µl
DMSO (1%)	0,5	0,5
Phusion Polymerase	0,5	0,5
H₂O	28,2	27,7
Total volume	50	50

PCR program:

PCR Program	temperature/ °C \|time
1	98	1'
2	98	15
8x	61	25
3	72	15
4	98	15
5	72	15
1x	72	5'
Hold	4

Digestion PCR product:

DNA-Concentration: 4,2 ng/µl

components	volume / µl
DNA	28,5
BSA 100x	0,4
Buffer: 4 10x	4
Enzyme 1 (XbaI)	1
Enzyme 2 (PstI)	1
H₂O	5,1
Total volume	40

Purification of PCR product: (QlAquick Gel Extraction Kit)

preparation of purification was made according to the standardprotocol

Comments: The wrong enzymes were used. Experiment has to be done tomorrow.

Test digestion pSB1C3_CFP_SDM SspI and PvuII

Investigator: Stefan

buffer used: 2; Restriction-enzymes used: Enzyme 1: ClaI ; Enzyme 2: BpmI ; Enzyme 3: SspI ; Enzyme 4: PvuII

Plasmids:

pSB1C3_SDM_SspI/PvuII P185 (first tree lanes, cut with different enzymes)
pSB1C3_RFC25_longlinker P105
pSB1C3_CFP P51.1

Components	P185/µL	P185/µL	P185/µL	P105/µL	P51.1/µL
DNA	18	18	18	4,8	6,8
BSA (10x)	2,5	2,5	2,5	2,5	2,5
Buffer 2 (10x)	-	-	-	2,5	2,5
Buffer 4 (10x)	2,5	2,5	2,5	-	-
Enzyme 1 ClaI (152)	0,5	0,5	0,5	-	-
Enzyme 2 BpmI (144)	0,5	0,5	0,5	-	-
Enzyme 3 SspI (68)	-	0,5	-	0,5	0,5
Enzyme 4 PvuII (50)	-	-	1	0,5	0,5
H₂O	1	-	0,5	14,2	12,2
Total volume	25	25	25	25	25

Incubation: 75 minutes

Agarosegel
0.5 g Agarose, 50 ml TAE, 3 µL GELRED, at 115 Volt, running time: 60 minutes

Freiburg10 SspI PvuII ClaI BpmI later.png

comments: Test digestion of pSB1C3_SDM_SspI/PvuII with ClaI, BpmI and SspI looks the same as with ClaI and BpmI. Therefore we can assume that there is no additional restriction site within the vector. But still the bands above 3000 bp cannotz be explained. A new test digestion will be performed tomorrow to check the size of the vector.
The approach cut with ClaI, BpmI and PvuII looks strange. Propably, PvuII does not work correctly. New PvuII-HF was ordered and delivered so this can be verified tomorrow.
pSB1C3_RFC25_longlinker digested with SspI and PvuII seems to be not completely digested This could correspond to non-working PvuII. pSB1C3_CFP looks like expected.

pSB1C3_SDM_Ssp1 (P125) sent for sequenzing

Investigator: Stefan

comment: To verify the correct deletion of the SspI restriction site it was sent for sequenzing.

Primer used: GATC_std_pTeSp-2

Picking clones of pSB1C3_SDM_SspI/PvuII (P185)

Investigator: Adrian

comment: pSB1C3_SDM_SspI/PvuII (P185) is empty. For plasmid production DYT + Cm was inoculated from the glycerol stock (B159).

87. labday 12.08.2010

XL1blue are ready to use

Investigator: Jessica
there are 60µl aliquots to use for one trafo

Mini-Prep of pSB1C3_SDM_SspI/PvuII and pMA_RC_insert

Investigator: Stefan

Gycerol stock was prepared for pMA_RC_insert and labeled B167. No glyerol stock for pSB1C3_SDM_SspI/PvuII because cells from earlier stock werer used for Mini-Prep.

Miniprep was performed according to protocol.

Samples were labeled:

pSB1C3_SDM_SspI/PvuII = P185.1
pMA_RC_insert = P190

Concentrations:

pSB1C3_SDM_SspI/PvuII (P185.1): 257,2 ng/µl
pMA_RC_insert (P190): 339,5 ng/µl

No test digestion was performed.

Biobrick Assembly: pSB1C3_lITR_CMV & pSB1C3_betaglobin_mVenus

Investigator: Chris L., Achim

Comments: In order to proceed with the BioBrick assembly the plasmids pSB1C3_leftITR_CMV was cut with SpeI and PstI, pSB1C3_betaglobin_mVenus was cut with XbaI and PstI. The insert fragment containing betaglobin_mVenus was ligated to the vector fragment containing the leftITR_CMV promotor.

Ligation:
For ligation, T4 ligase was used.

1µl T4-Ligase buffer (10x)
8µl (Vector + Insert) mix
1µl T4-Ligase

Ligation was carried out as following:

pSB1C3_leftITR_CMV: 6,98 µl
pSB1C3_betaglobin_mVenus: 1,02 µl

Incubation for 40 minutes.

Transformation:

The transformation was done following the standard protocol using XL1B cells.

Repetition of cloning of bla14FM_viralbrick_MCS into pSB1C3_SDM_SspI

Investigator: Anissa

Comments:Yesterday the pcr-product of bla14FM was cut with the wrong enzymes, so no overhangs could result. Today it will be repeated with the rihgt ones (SpeI and NgomIV) .

Digestion of the PCR product bla14FM for 2 h :

DNA-Concentration: 10,2 ng/µl

components	volume / µl
DNA	18
BSA 100x	3
Buffer: 4 10x	3
Enzyme 1 (NgomIV)	1
Enzyme 2 (SpeI)	1
H₂O	4
Total volume	30

Purification of PCR product: (QlAquick Gel Extraction Kit)

preparation of purification was made according to the standardprotocol

Digestion of vector backbone pSB1C3_SDM_SspI for 2 h:

1 µg vector has been used

components	volume / µl
DNA	3,12
BSA 100x	1,5
Buffer: 4 10x	1,5
Enzyme 1 (NgomIV)	1
Enzyme 2 (SpeI)	1
H₂O	6,88
Total volume	15

the cut vector was loaded on a preperative 1% agarose gel and the gel was running for 45 minutes

gel was cut and gelextraction was performed according the qiagen standard protocol.

Ligation of pSB1C3_SDM_SspI and bla14FM:

components	volume / µl
t4 buffer (10X)	1
t4 Ligase	1
vector DNA	2,72
Insert	5,28

Transformation: pSB1C3_SDM_SspI_bla14FM was transformed into BL21 following the stanard protocol

Quickchange of the EaglII restriction site in the PMA_RepCap vector

Investigator: Chris L., Achim

Comments: We performed a QuikChange mutagenesis on the synthesized PMA_RepCap vector (P190). The EaglII restriction enzyme also cuts NotI (IGEM standard) therefore EaglII has to be changed into a different recognition site. Primers were designed to change it into PvuII. The new QuikChange Lighting Site-Directed Mutagenesis Kit from Stratagene was used, therefore the mutagenesis was carried out as described in the QuikChange Manual. The PCR product was transformed into XL10-Gold cells, we used the IGEM standard protocol, except for the addition of ß-ME to the XL10-Gold cells. :

PCR-reaction:

Volume / µl	ingredients	recommended /µl
2,5	10X reaction buffer	2,5
2,9	P190 template (~10 ng)	2,9 of 1:100 dilution
0,51	forward primer: O122	62,5 ng
0,51	reverse primer: O123	62,5 ng
0,5	dNTP	250 µM each dNTP
17,6	H₂O
0,5	QuikChange Lightning ennzyme(1.25)

PCR program:

Rounds	temperature/ °C	Time
1	95	2 minutes
18	95	20 seconds
18	60	10 seconds
18	68	2 minutes (4 kb * 30 sec)
1	68	5 minutes

The PCR product was digestet with Dpn I for 10 minutes at 37°C

Plasmid was transformed into XL10-Gold cells.

Sequencing results of Rep68, Rep78 and AAP BioBricks

Investigator: Hanna
Comment: pSB1C3_Rep78 (P160), pSB1C3_Rep68 (P165) and pSB1C3_AAP (P170) were sent for sequencing twice. No sequencing made sense. Paradoxically the Rep78 sequencing result fit to the p5 promoter BioBrick...
By having a closer look to the BioBrick PCR we found out that the fragment sizes didn't fit to the expected sequences. In addition to that the test digestion also showed some discrepancies.
Because we weren't able to find out in which steps of the BioBrick production things went wrong, we decided to discard all referring glycerol stocks and plasmids and to perform the Rep68, Rep78 and AAP BioBrick PCR again!!!

Comment 13.08.2010 (Hanna): We wondered how the whole Rep stuff could be sequenced reverse AND forward without any forward sequencing primer... By checking the "sequencing book" we found out that always the wrong primers were used: the GOI primers can be used in order to sequence the Gene of interest = GOI (!) in pAAV_MCS and NOT the pSB1C3!!!!!!!!!

Order oligos for CD-biobrick

Investigator: Jessica and Kira
ordered on aug 12th

BioBrick assembly of pSB1C3_leftITR_CMV_mVenus

Investigator: Stefan

comment: In order to assemble our complete constructs mVenus has to be included into the pSB1C3_leftITR_CMV vector.
Digestion:

components:	pSB1C3_leftITR_CMV P188(Vector)	pGA14_mVenus P60 (Insert)
DNA	6	8
BSA (10x)	2	2
Buffer 4 (10x)	2	2
Enzyme1	1 (SpeI)	1 (Xba1)
Enzyme2	1 (PstI)	1 (PstI)
H2O	8	6
Total volume	20	20

Preparation of gel:
0,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 110 Volt, running time: 45 minutes

Expected sizes of constructs:

pSB1C3_leftITR_CMV: 2869 bp
pGA14_mVenus: 2896 bp, 756 bp

The corresponding bands were cut out and Gel-Extraction was performed according to protocol.

concentrations measured via NanoDrop:

pSB1C3_leftITR_CMV: 39,2 ng/µl
pGA14_mVenus: 8,2 ng/µl

Ligation:

T4 ligation was performed according to protocol.

Volumes used:

vector: 1,67 ng/µl
insert: 6,33 ng/µl

Transformation:

bacterial strain used: XL1bB

antibiotic used for plate: chlorampenicol

Transformation was performed according to protocol.
Plate was prepared and put in 37°C room.

Opened a BioBrick box

Investigator: Bea
In order to "save" the plasmids/BioBricks which has been prepared and confirmed for submitting it to the parts registry a new box have been prepared. The box should contain 30 µL of the desired construct cloned into the pSB1C3 vector and the BBa number given from the headquarter.

Freiburg10 BioBrick highlighting in Nomenclature list.JPG

The first BioBricks which are in this box are:

pSB1C3_hGH (P136): Bba_K404002
pSB1C3_betaglobin (P133: Bba_K404001
pSB1C3_CMV (P145): Bba_K404003
pSB1C3_leftITR (P175): Bba_K404006
pSB1C3_rightITR (P172): Bba_K404005
pSB1C3_mGMK (P156): Bba_K404004

In our nomenclature plasmid excel list the constructs which we aliquoted should be highlighted in blue and commented with the given Bba number. Additionally it should be taken in consideration that enough DNA should be in the "working" plasmid box. Therefore, if necessary, inoculate DYT medium for Mini-Preps.

In this case ALL the glycerol stocks were used for incoluating 10 mL DYT medium containing 10 µL chloramphenicol respectively.

To do: Mini-Preps of the over night cultures.

88. labday 13.08.2010

Continuation:pSB1C3_SDM_SspI_bla14FM

Investigator: Patrick
Intention: receive enough plasmid for a sequencing and maybe futher working steps.
Three clones were picked in the morning to inoculate DYT and perform a mini-prep in the evening and to send them for sequencing. The three clones were picked and prepped according to the standard protocol yielding the following DNA concentrations:

pSB1C3_SDM_SspI_bla14FM clone 1: 65,15 ng/µl , Sequencing labeled: PS3.1
pSB1C3_SDM_SspI_bla14FM clone 2: 22,3 ng/µl , Sequencing labeled: PS3.2
pSB1C3_SDM_SspI_bla14FM clone 3: 62,3 ng/µl , Sequencing labeled: PS3.3

Used primer: seq_pSB1C3_VR2_rev (O51)
Results: see http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/index.php/Laborjournal#Sequence_analysis_of_pSB1C3_SDM_SspI_BLA

Mini-preps of pSB1C3_hgh,pSB1C3_beta globin,pSB1C3_left ITR,pSB1C3_right ITR,pSB1C3_mGMK,pSB1C3_CMV

Comments:new mini-preps of the glycerol-stocks ofpSB1C3_hgh(=B103),pSB1C3_beta globin(=B100),pSB1C3_left ITR (=B143),pSB1C3_right ITR (=B140),pSB1C3_mGMK (=B125),pSB1C3_CMV :

components	concentration in ng/µl
P191 (pSB1C3_right ITR)	100,74
P192 (pSB1C3_beta-globin)	240,08
P193 (pSB1C3_CMV)	333,89
P194 (pSB1C3_hgh)	328,42
P195 (pSB1C3_mGMK)	258,63
P196 (pSB1C3_left ITR)	173,98

Design and ordering of oligos for VP fusion targeting approaches

Investigator: Hanna

Comment: In order to target the EGFR receptor of our A431 cells different approaches have been figured out: Besides loop insertions, N-terminal fusion to the VP2 protein will be performed. In addition to that a VP1 insertion approach (after Grieger et al., 2007) was planned.
Fusion and insertion molecules will be e.g. His-tag, Affibody, Darpin, GFP. These approaches can be combinated with the loop insertions.
For this purpose the following oligos were ordered today:

Mini-Prep and Test digestion of Rep40 and Rep52 of the cloning experiment ("Cloning of Rep40/52" 11.08.2010 Investigator: Anna)

Investigator: Chris L., Achim

Comments: There are small and big colonies on the plate. Maybe problems with the agar plate. Picked colonies of pSB1C3_Rep40 sample 1 and pSB1C3_Rep52 sample 1 are small colonies. Picked colonies of pSB1C3_Rep40 sample 2 + 3 and pSB1C3_Rep52 sample 2 + 3 are standard size colonies.

Nanodrop

Rep 40 Sample 1: 156,26 ng/µl P197
Rep 40 Sample 2: 200,05 ng/µl P198
Rep 40 Sample 3: 144,06 ng/µl P199
Rep 52 Sample 1: 173,36 ng/µl P200
Rep 52 Sample 2: 160,75 ng/µl P201
Rep 52 Sample 3: 295,77 ng/µl P202

Test digestion 800ng DNA

components	P145 /µl	P146 /µl	P145 /µl	P146 /µl	P145 /µl	P146 /µl
DNA	5,1	4	5,6	4,6	5	2,7
BSA (10x)	2	2	2	2	2	2
Buffer 4 (10x)	2	2	2	2	2	2
Enzyme 1: XbaI	0,5	0,5	0,5	0,5	0,5	0,5
Enzyme 2: SpeI	0,5	0,5	0,5	0,5	0,5	0,5
H₂O	9,9	11	9,4	10,4	10	12,3
Total volume (e.g. 15,20,25,30 µl)	20	20	20	20	20	20

Incubation time: 45 minutes, Incubation temperature: 37°

0,5 g Agarose, 50ml x TAE, 3µl GELRED, at 115 Volt, running time: 45 minutes

Sample	Sample/µl]	Loading dye (6x)/µl	Expected size 1 (Geneious)	Expected size 2 (Geneious)
Rep 40 1	20 µl	4 µl	____ bp	940 bp
Rep 40 2	20 µl	4 µl	____ bp	940 bp
Rep 40 3	20 µl	4 µl	____ bp	940 bp
Rep 52 1	20 µl	4 µl	____ bp	1198 bp
Rep 52 2	20 µl	4 µl	____ bp	1198 bp
Rep 52 3	20 µl	4 µl	____ bp	1198 bp

	Marker	Sample Rep40 1 /20µl	Sample Rep40 2 /20µl	Sample Rep40 3 /20µl	Sample Rep52 1 /20µl	Sample Rep52 2 /20µl	Sample Rep52 3 /20µl
Lane	1	2	3	4	5	6	7

agarose gel: 1%, digestion: 45 minutes, 37°C

Comments:Results look bad. Rep52 clone 3 looks good, send for sequencing.

</p>

Repetition of Rep 40 and Rep 52 ligation and transformation with the vector pSB1C3_CFP

Investigator: Chris L.

Ligation of PCR products and vector:

For the Ligation 1µl T4 buffer (10x) and 1µl T4 ligase were used.

	Sample-no.	vector /µl	insert /µl
pSB1C3 + Rep40	1	4,92	3,08
pSB1C3 + Rep52	2	6,47	1,53
Total volume (e.g. 15,20,25,30 µl)		10	10

Transformation:

The transformation was done following the standard protocol using XL1B cells.

Strategy for VP2 N-terminal fusion and VP1 insertion of targeting moelcules

Investigator: Hanna

Comment: In order to target the EGFR receptor of tumor cells via Affibody or Darpin (antibody fragment is also possible!!!), or in order to expose e.g. His-Tags on the virus surface, two approaches have been figured out.

File:Freiburg10 N-terminalFusion Strategy3.JPG

pSB1C3_Rep52 (P202) sent for sequencing

Investigator: Chris L.

Primer used: Reverse Primer VR2

<p style="font-size:15px; background-color:#66bbff;">Repetition: Biobrick production of Rep 68, 78 and AAP

Investigator: Stefan

Aim of the experiment: We want to produce biobricks from Rep 68, Rep 78 and the AAP.

Plasmids used as template:

Rep_68_ex (p119): c = 470,6 ng/µl
Rep_78_(p122): c = 566,8 ng/µl
pAAV-RC containing AAP ORF (p50): c = 378,5 ng/µl

Primer used:

For Rep_68_ex: Praefix_68_78_ex & Suffix_40_68_ex
For Rep_78_ex: Praefix_68_78_ex & Suffix_52_78_ex
For AAP_ex: Praefix_AAP_ex & Suffix_AAP_ex

PCR:

(was performed following the standard protocol)

Ingredients	Volume / µl	Rep68	Rep78	AAP
5X Phusion HF buffer	10
10 mM dNTP mix	1
forward primer:	2,5
reverse primer:	2,5
DNA Template	***	2,5 µl	2 µl	3 µl
DMSO (2%)		-	-	1 µl
Phusion Polymerase	0,5
H₂O	***	31 µl	31,5 µl	29,5 µl
Total volume	50

PCR program:

PCR Program	temperature/ °C	Time	Rep68	Rep78	AAP
1	98	1min
2	98	15s
3	***	25s	63°C	62°C	64°C
4 (step 2-4 8x)	72	***	24s	27s	10s
5	98	15s
6	***	25s	68°C	64°C	68°C
7	72	***	24s	27s	10s
8 (step 6-8 17x)	72	5min
Hold	4

Used agarose gel: 0,5 g Agarose,50 ml TBE (1%), 3 µl GELRED , at 115 Volt, running time:45 minutes

Gel extraction

Gel extraction was perfomed according to protocol.

Digestion of PCR products and vector:

components	PCR products /µl	vector /µl
DNA	29	11
BSA (10x)	4	2
Buffer 4 (10x)	4	2
Enzyme XbaI	1	1
Enzyme SpeI	1	1
H2O	1	3
Total volume (e.g. 15,20,25,30 µl)	40	20

Comments: Digestion was done with XbaI and SpeI, it has to be checked if the inserts are cloned into the vector in the right orientation.

Purification of Rep68, 78 and AAP:

For the purification 200 µl of buffer PBI was used.

c(Rep68)= 14,3 ng/µl
c(Rep78)= 12,0 ng/µl
c(AAP)= 25,1 ng/µl

Gelextraction of pSB1C3_RFC25_CFP:

0,5 g Agarose,50 ml TBE (1%), 3 µl GELRED , at 115 Volt, running time:50 minutes
4µl loading dye (6x) for the sample, Marker: GeneRuler ladder mix (Fermentas)

c(pSB1C3)= 6,9 ng/µl

T4 ligation of PCR products and vector:

For the Ligation 1µl buffer (10x) and 1µl T4 ligase were used.

	vector /µl	insert /µl
pSB1C3 + Rep68	3,78	4,24
pSB1C32 + Rep78	3,13	4,87
pSB1C3 + AAP	6,42	1,58

Transformation:

The transformation was done following the standard protocol using XL1b cells.

89. labday 14.08.2010

Sequence analysis of pSB1C3_SDM_SspI_BLA

Investigator: Patrick, Bea

Comments: Sequence analysis of three clones revealed that all sequences contain some mutations in the regions where the primer annealed. This was due to the extreme primer lentgh. Primers that long should be ordered as HPLC purified in order to avoid mutations in the primer sequence.

Clone 1: Mutation in the SalI site of the loop insertion site in the Viral Brick MCS lead to the removal of the recognition site. CANNOT be used for the loop insertions!!!!
Clone 2: Mutation in the region of the primer upstream of the loop insertion sites SalI and PvuII.
Clone 3: Mutation in the region of the primer downstream of the loop insertion sites SalI and PvuII.

Sequencing results of pSB1C3_SDM of SspI_BLA clone 2 and pSB1C3_SDM of SspI_BLA clone 3
Clone 2	Clone 3

Next steps: Two additional clones will be picked and sent for sequencing (clones 4 and 5). In order to obtain a construct without any mutations, clone 2 and clone 3 couldbe cloned together. Each clone will be digested with SalI and BamHI. Clone 2 will be the "insert", clone 3 is going to be the "vector". Therefore the fragments will (hopefully) not contain anymore mutations in the relevant sequence.

Mini Preps of PMA_RepCap vector and pSB1C3_left ITR_CMV_betaglobin_mVenus

Investigator: Chris L., Bea

Comments:new mini-preps of the glycerol-stocks of pSB1C3_leftITR_CMV_betaglobin_mVenus clone 1 (=B179), pSB1C3_leftITR_CMV_betaglobin_mVenus clone 2 (=B180), pSB1C3_leftITR_CMV_betaglobin_mVenus clone 3 (=B181), pMA_RepCap Vector_SDM_InsPvuII clone 1, (=B182), pMA_RepCap Vector_SDM_InsPvuII clone 2 (=B183) and pMA_RepCap Vector_SDM_InsPvuII clone 3 (=B184)

Comment: The plamsid numbers in the picture (P179-P184) correspond to the glycerol stocks B179-B184. The corresponding plasmid numbers are: P208-P213.
Nanodrop

pSB1C3_leftITR_CMV_betaglobin_mVenus clone 1: 256,64 ng/µl B179
pSB1C3_leftITR_CMV_betaglobin_mVenus clone 2: 274,86 ng/µl B180
pSB1C3_leftITR_CMV_betaglobin_mVenus clone 3: 217,20 ng/µl B181
pMA_RepCap Vector_SDM_InsPvuII clone 1: 253,71 ng/µl B182
pMA_RepCap Vector_SDM_InsPvuII clone 2: 195,64 ng/µl B183
pMA_RepCap Vector_SDM_InsPvuII clone 3: 144,61 ng/µl B184

Test digestion 800ng DNA

components	B179 /µl	B180 /µl	B181 /µl	B182 /µl	B183 /µl	B184 /µl	pMA_RepCap Vector /µl
DNA	3,1	2,9	3,7	3,1	4	5,5	2,4
BSA (10x)	2	2	2	2	2	2	2
Buffer 4 (10x)	2	2	2	2	2	2	2
Enzyme 1: NgoMIV	0,5	0,5	0,5	0	0	0	0
Enzyme 2: EcoRI	0,5	0,5	0,5	0	0	0	0
Enzyme 2: PvuII	0	0	0	0,5	0,5	0,5	0,5
H₂O	11,9	12,1	11,3	12,4	11,5	10	13,1
Total volume (e.g. 15,20,25,30 µl)	20	20	20	20	20	20	20

Incubation time: 45 minutes, Incubation temperature: 37°

0,5 g Agarose, 50ml x TAE, 3µl GELRED, at 115 Volt, running time: 45 minutes

Results of test digestion

Results: Two (three) different approaches can be seen on the agarose gel.

P178-P181 (blue): The plasmid pSB1C3_leftITR_CMV_betaglobin_mVenus was digested with NgoMIV and EcoRI. Expected bands were: 2873bp and 1343 . As it can be seen in the picture, the two fragments ran too high (~300bp). As it is almost normal for the pSB1C3 plasmid, we should figure out why this is always the problem for this vector.
P182-P183 (red): The plasmid pMA_RepCap_SDM_insPvuII was digested with PvuII as well as the control vetor pMA_RepCap where no site-directed mutagenesis was performed in order to see the difference. As it can be seen in the picture above, the expected band sizes of 263bp,1384bp and 2133bp correspond to the bands detected in the gel. The control vector instead reveals only two bands detectable. Therefore site-directed mutagenesis was successfully performed.
P177 (green): pSB1C3_hTERT. For further details see extra part below (Test digestion of pSB1C3_hTERT.

Mini-Prep of pSB1C3_leftITR_CMV_mVenus

Investigator: Stefan

Glycerol stocks were prepared:

B177 = pSB1C3_leftITR_CMV_mVenus clone 1

B178 = pSB1C3_leftITR_CMV_mVenus clone 2 Mini-Prep following the standard protokol

P206 = pSB1C3_leftITR_CMV_mVenus clone 1 = 277,9 ng/µl

P207 = pSB1C3_leftITR_CMV_mVenus clone 2 = 260,3 ng/µl

Test digestion: or test digestion, pSB1C3_leftITR_CMV (P188) was digested as well.

Ingredients	clone 1/µl	clone 2/µl	P188/µl
DNA:	3,5	3,5	4
BSA (10x):	2	2	2
Buffer 4:	2	2	2
Enzyme 1 EcoRI:	0,5	0,5	0,5
Enzyme 2 AgeI	0,5	0,5	0,5
H₂O	6,5	6,5	6

GeneRuler Ladder Mix (7µl)
P206 = pSB1C3_leftITR_CMV_mVenus clone 1
P207 = pSB1C3_leftITR_CMV_mVenus clone 2
P188 = pSB1C3_leftITR_CMV

comment: Through digestion, fragments would have similar sizes. Therefore, a new digestion will be performed tomorrow.

Test digestion of pSB1C3_pHTERT

Investigator: Bea

Comments: pSB1C3_hTERT was sent for sequencing and revealed that the PCR and the inserting of the PCR product : promoter for hTERT was sucessfully performed. But the sequencing results showed a new AgeI restriciton site in the plasmid backbone. We could not see if the new recognition site was due to the bad sequence read or that there is really a new AgeI site. Therefore, a test digestion will be perfomed with PstI and AgeI in order to figure our wheter AgeI is present in the backbone or not.

Sequence analysis of pSB1C3_hTERT:

Sequencing results of pSB1C3_hTERT

First the sequenced plasmid P177 was digested:

	P177/µL
DNA	3
BSA (10x)	1,5
Buffer 4 (10x)	1,5
Enzyme PstI	0,5
Enzyme AgeI	0,5
H2O	8
Total volume	15

Incubation time: 45minutes
Incubation tempereature: 37°C

After the incubation,the samples were loaded on the 1% agarose gel, and run at 110 V for 45 minutes.

Result of the test digestion:

Test digestion of pSB1C3_hTERT

Results: As it can be seen in the sequencing results of pSB1C3_hTERT there could have been an additional AgeI site in the vector. If AgeI would have been in the vector, two fragments have been expected by digetsing the plasmid with AgeI and PstI. As it can be seen in the agarose gel, lane 11 (labeled with the green P177) only reveals one lane instead of two. Therefore it can be assumed that NO AgeI site is in the pSB1C3 backbone.

Picking clones ...

Investigator: Patrick 15 Clones were picked saturday night so that a mini-prep could be performed on sunday.

90. labday 15.08.2010

Sequence analysis of pSB1C3_Rep52

Investigator: Bea

Comments: Clone 3 was sent for sequencing because this clone revealed the right band sizes of the test digestion performed friday. For more details see: [http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/index.php/Laborjournal#Mini-Prep_and_Test_digestion_of_Rep40_and_Rep52_of_the_cloning_experiment_.28.22Cloning_of_Rep40.2F52.22_11.08.2010_Investigator:_Anna.29 Test digestion]

Sequencing results of pSB1C3_Rep52 clone 3

Results:

Sequence assembly showed that the suffix of the Rep protein 52 is ok and that PCR worked well.

There can be seen that a silent mutation from AGG to AGA was inserted, but it will have no effect on the protein because codon usage in H. sapiens is nearly the same for both codons.

The prefix could not be analysed because of bad sequence read quality. For further verification, another sequencing with the forward primer has to be performed.
Next steps: Send plasmid for another sequencing round with forward primer in order to analyse the prefix.

[http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/index.php/Laborjournal top of page]

Mini-Prep of pSB1C3_Rep68, pSB1C3_Rep78, pSB1C3_RepAAP, pSB1C3_Rep40, pSB1C3_Rep52

Investigator: Stefan

Glycerol stocks were prepared:

B185 = pSB1C3_Rep68 clone 1
B186 = pSB1C3_Rep68 clone 2
B187 = pSB1C3_Rep68 clone 3
B188 = pSB1C3_Rep78 clone 1
B189 = pSB1C3_Rep78 clone 2
B190 = pSB1C3_Rep78 clone 3
B191 = pSB1C3_AAP clone 1
B192 = pSB1C3_AAP clone 2
B193 = pSB1C3_AAP clone 3
B194 = pSB1C3_Rep40 clone 1
B195 = pSB1C3_Rep40 clone 2
B196 = pSB1C3_Rep52 clone 1
B197 = pSB1C3_Rep52 clone 2
B198 = pSB1C3_SDM_SspI_Bla14FM clone 4
B199 = pSB1C3_SDM_SspI_Bla14FM clone 5

Mini-Prep following the standard protokol
P208 = pSB1C3_Rep68 clone 1 c=230,0
P209 = pSB1C3_Rep68 clone 2 c=160,5
P210 = pSB1C3_Rep68 clone 3 c=128,6
P211 = pSB1C3_Rep78 clone 1 c=150,8
P212 = pSB1C3_Rep78 clone 2 c=108,6
P213 = pSB1C3_Rep78 clone 3 c=131,3
P214 = pSB1C3_AAP clone 1 c=142,1
P215 = pSB1C3_AAP clone 2 c=148,3
P216 = pSB1C3_AAP clone 3 c=163,0
P217 = pSB1C3_Rep40 clone 1 c=164,5
P218 = pSB1C3_Rep40 clone 2 c=<145,1br />
P219 = pSB1C3_Rep52 clone 1 c=156,0
P220 = pSB1C3_Rep52 clone 2 c=164,0
P221 = pSB1C3_SDM_SspI_Bla14FM clone 4 c=220,4
P222 = pSB1C3_SDM_SspI_Bla14FM clone 5 c=252,2

Test digestion:
No test digestion for pSB1C3_SDM_SspI_Bla14FM clone 4 and 5.
For test digestion, pSB1C3_leftITR_CMV_mVenus (P206-207) and pSB1C3_leftITR_CMV (P188) was digested as well.
Samples P208-220 were digested with XbaI and SpeI.
Samples P207, P207 and P188 were digested with XbaI and NgoMIV.

Gel used:
100 ml TAE (1x), 1 g agarose, 6 µl GELRED
115 V, 50 minutes

Ingredients	P208/µl	P209/µl	P210/µl	P211/µl	P212/µl	P213/µl	P214/µl	P215/µl	P216/µl	P217/µl	P218/µl	P219/µl	P220/µl	P206/µl	P207/µl	P188/µl
DNA:	4	6	7	6	9	7	6	6	6	6	6	6	6	3,5	3,5	4
BSA (10x):	2	2	2	2	2	2	2	2	2	2	2	2	2	2	2	2
Buffer 4:	2	2	2	2	2	2	2	2	2	2	2	2	2	2	2	2
Enzyme 1	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5
Enzyme 2	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5	0,5
H₂O	11	9	8	9	6	8	9	9	9	9	9	9	9	11,5	11,5	11

comment: Rep- and AAP approaches have to be repeated. We did not realize that the vector can religate! Plasmids and glycerol stocks were thrown away.

Inoculation of CD colony

Investigator: Kira

One colony was picked from agar plate and dispersed into 10 ml DYT+ Amp and incubated over night @ 37 C.

@@ Line 122: / Line 122: @@
 <div class="box_right">
 </html>
-==September==
+===76.Labortag 01.08.2010===
-===107. labday 01.09.2010===
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Picking clones of pSB1C3_CMV</b></p>====
-====<p style="font-size:15px; background-color:#66bbff;"><b>Loop insertion BioBricks: Sequencing results</b></p>====
+<p><b>Investigator: Bea</b></p>
-<b>Investigator: Achim, Anna <br /></b>
+<p style="font-size:13px; color:#66bbff;"><b>Comments:</b> Trafo was performed friday, and trafo plate were incubated over night. Clones need to be picked in order to perform Mini-Prep</p>
-<p style="font-size:13px; color:#66bbff;">Comment: Sequencing results of Loop insertion BioBricks from 31.08.10; the following clones were sent for sequencing: </p>
+<ul>
+<li>Bacterial strain used: XL1-B</li>
+<li>Two clones were picked of trafo plate</li>
+<li>Inoculating of 10 mL DYT medium containing 10µL chloramphenicol</li>
+<li> Put in 37°C room on rotary shaker</li>
+</ul><br>
+===77.Labortag 02.08.2010===
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Sequenzing of pSB1C3_RFC25_longlinker, pSB1C3_RFC25_SEG, pSB1C3_RFC25_GSAT </b></p>====
+'''Investigator: Jessica'''<br>
+<p style="font-size:13px; color:#66bbff;"><b>Comments:</b> Linkers (we got from Gerrit) we cloned in the RFC25-standard (pSB1C3_RFC25). Result looks good, linkers are in the vector pSb1C3_RFC25 <br>
+<ul><li>pSB1C3_RFC25_longlinker '''P105 und P106'''</li>
+<li>pSB1C3_RFC25_SEG '''P107 und P108'''</li>
+<li>pSB1C3_RFC25_GSAT '''P109 und P110'''</li>
+</ul>
+</p>
+[[File:Freiburg10_Sequence_alignment_longlinker.jpg|500px|left|thumb|]]
+[[File:Freiburg10_Sequence_alignment_SEG.jpg|500px|left|thumb|]]
+[[File:Freiburg10_Sequence_alignment_GSAT.jpg|500px|left|thumb|]]
+<p style="clear:both;"> </p>
+<br>
+<br>
+====<p style="font-size:15px; background-color:#FF00FF;"><b>Sequencing of pGA14_Prefix-leftITR</b></p>====
+'''Investigator: Hanna'''<br>
+<br>
+Eventually GATC partially managed to sequence pGA14_Prefix-left ITR clone 1 and 2. <br>
+The sequencing results were better than before but in the ITR region still not evaluable due to the strong secondary structures. <br>
+<br>
+It seemed that, despite of successful insertion of the RFC10-Prefix, something went wrong because there were 2 bases missing in the NotI restriction site. But by having a closer look, it became obvious that the Geneious misinterpreted the chromatogram and overlaid the peaks of the missing bases. <br>
+<br>
+[[File:leftITR+Prefix.jpg|800px]]
+<br>
+<br>
+For the first time sequencing of parts of the 3' end worked: The remaining NotI restriction site, which was already eliminated this week and also the "backbone-PstI" can be seen: <br>
+<br>
+[[File:leftITR+Prefix_2.jpg|800px]]
+<br>
+<br>
+Sequencing of very GC-rich regions :) :) :) <br>
+<br>
+[[File:leftITR+Prefix_3.jpg|800px]]
+<br>
+<br>
+Sequencing of clone 4 delivered that the ITR and the RFC10-Prefix were not inserted in the vector. The RFC25 standard of the multiple cloning site is still in the plasmid: <br>
+<br>
+[[File:LeftITR+Prefix clone4.jpg|800px]]
+<br>
+<br>
+Therefore clone 4 was dicarded from the plasmid- and glycerol stock. <br>
+<br>
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Repetition of test digestion pSB1C3_CFP SDM SspI and PvuII </b></p>====
+'''Investigator: Jessica'''<br>
+*buffer used: 2; Restriction-enzymes used: Enzyme 1: SspI ; Enzyme 2: PvuII
+<ul><li>Plasmids (all: ~ 700 ng/µL):</li>
+<ul><li>pSB1C3_CFP '''P51.1'''</li>
+<li>pSB1C3_SDM_SspI '''P125'''</li>
+<li>pSB1C3_SDM_PvuII '''P129'''</li>
+<li>pSB1C3_SDM_PvuII '''P131'''</li></ul>
+</ul>
+<br />
+{| border="1"
+| align="left" | '''Components'''  ||align="left"| '''Mastermix'''  ||align="left"| '''P125/µL''' ||align="left"| '''P51.1.1/µL''' ||align="left"| '''P129/µL''' ||align="left"| '''P131/µL''' ||align="left"| '''P51.1.2/µL'''
+|-
+| align="left" | DNA  ||align="left"| -||align="left"| 2,4||align="left"| 2,3||align="left"| 1,6||align="left"| 5,3||align="left"|5,3
+|-
+| align="left" | BSA (10x) ||align="left"| 6||align="left"| 1||align="left"| 1||align="left"| 1||align="left"| 1||align="left"| 1
+|-
+| align="left" | Buffer 2 (10x)  ||align="left"| 6||align="left"| 1||align="left"| 1||align="left"| 1||align="left"| 12||align="left"| 1
+|-
+| align="left" | Enzyme 1 SspI (68)  ||align="left"|-||align="left"| 1||align="left"| 1||align="left"| -||align="left"| -||align="left"| -
+|-
+| align="left" | Enzyme 2 PvuII (50)  ||align="left"| -||align="left"| -||align="left"| -||align="left"| 1||align="left"| 1||align="left"| 1
+|-
+| align="left" | H<sub>2</sub>O ||align="left"| -||align="left"| 4,6||align="left"| 4,7||align="left"| 5,4||align="left"| 1,7||align="left"| 1,7
+|-
+| align="left" | '''Total volume'''  ||align="left"| 12||align="left"| 10||align="left"| 10||align="left"| 10||align="left"| 10||align="left"| 10
+|}
 <br />
-*2: 453 BAP: No Insert
-[[File:Freiburg10 453 bap.JPG|400px]]
-*3:453 His: Insert okay
-[[File:Freiburg10 453 his.JPG|400px]]
-*5: 453 RGD: Mutation in 453 upstream region
-[[File:Freiburg10 453 rgd.JPG|400px]]
-*7: 587 BAP: Mutation in Bap insert
-[[File:Freiburg10 587 bap.JPG|400px]]
-*9:587 His: Insert okay
-[[File:Freiburg10 587 his.JPG|400px]]
-*11:587 KO BAP : Insert okay
-[[File:Freiburg10 587 KO bap.JPG|400px]]
-*13:587 KO empty : Insert okay
-[[File:Freiburg10 587 KO empty.JPG|400px]]
-*16: 587 KO his: Mutation in 587 KO
-[[File:Freiburg10 587 ko his.JPG|400px]]
-*17: 587 KO rgd: No insert
-[[File:Freiburg10 587 KO rgd.JPG|400px]]
-*19 :587 RGD: Insert okay
-[[File:Freiburg10 587 rgd.JPG|400px]]
-*25: 587 Z34C: Mutation in downstream 587 region
-[[File:Freiburg10 587 z34c.JPG|400px]]
-<b>Mini-Preps:<br /></b>
+*Incubation: 65 minutes<br>
+'''Agarosegel'''
+<br />
+.45 g Agarose, 50 ml TEB (0,5 %), 3 µL GELRED, at 115 Volt, running time: 45 minutes
+<br />
+<br />
-New Mini-Preps of the samples with no/mutated insert were prepared. The following clones were used:
+<ul><li>Marker: GeneRuler ladder mix (6x)</li></ul>
+{| border="1"
+|
+!Marker
+!P125
+!P51.1 SspI
+!-
+!P129
+!P131
+!P51.1 PvuII
+|-
+!Lane
+|7 µL
+|10 µL
+|10 µL
+| -
+|10 µL
+|10 µL
+|10 µL
+|-
+|}
+<br />
+[[File:Freiburg10_Gel test digestion SDM.jpg|500px|left|thumb|]]
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<ul><li>'''P125''' isn't cut, therefore you see the bands for supercoiled, nicked and relaxed</li>
+<li>'''P51.1''' is cut once, therefore you can see a faster running band</li>
+<li>'''P129''' and '''P131''' should be cut once because of the PvuII in the CFP but there is another band we can't identify</li>
+<li> '''P51.1''' should be cut two times but there is also another unidentified band</li>
+<ul><li>perhaps there is another PvuII in the vector we can't find (???)</li></ul>
+</ul>
+<p style="font-size:13px; color:#66bbff;"><b>Comments:</b> SDM of SspI is ready! SDM of PvuII looks confusing because of the lower band. P 129 will be sequenced but this doesn't solve this problem. there has to be one more rs we don't know, perhaps. we will check it...anywise</p><br>
+====<p style="font-size:15px; background-color:#66bbff;">'''Mini-Prep and Test digestion of pSB1C3_CMV  '''</p>====
+'''Investigator: Kerstin''' <br>
+'''Nanodrop'''
+* pSB1C3_CMV clone1: 157,6 ng/µl '''P145'''
+* pSB1C3_CMV clone2: 155,6 ng/µl '''P146'''
+<br>
+<br>
+'''Test digestion''' 900ng DNA
 {| border="1"
+| components   || align="right" |P145 /µl || align="right" |P146 /µl
+|-
+| DNA  ||  align="right" | 5,7||  align="right" |5,8
+|-
+| BSA (10x) ||  align="right" |1,5 ||  align="right" | 1,5
+|-
+| Buffer 4 (10x)||  align="right" | 0,5 ||  align="right" | 0,5
+|-
+| Enzyme 1: XbaI ||  align="right" | 0,5 ||  align="right" | 1,5
+|-
+| Enzyme 2: PstI ||  align="right" | 0,5 ||  align="right" | 0,5
+|-
+|H<sub>2</sub>O||  align="right" | 5,3||  align="right" | 5,2
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | '''15'''||  align="right" | '''15'''
+|}
+<br>
+agarose gel: 1,5%, digestion: 90 minutes, 37°C
+<br>
+[[File:Freiburg 10 pSB1C3 CMV.jpg|400px|thumb|left|]]
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
-|align="left" | '''Components''' ||align="left"| '''453 BAP''' ||align="left"| '''587 BAP''' ||align="left"| '''453 RGD'''||align="left"| '''587 KO RGD'''||align="left"| '''587 KO HIS'''||align="left"| '''453 Z34C'''||align="left"| '''587 Z34C'''||align="left"| '''587 KO Z34C'''||align="left"| '''587 KO Z34C SPACER'''
+'''P145 is sent for sequencing with Reverse Primer (VR2)'''
+<p style="font-size:13px; color:#68bbff;">'''''Comments:'''''Results look good. CMV has the expected size (~ 662bp) </p><br>
+ '''</p>
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Sent for sequencing</b></p>====
+'''Investigator: Jessica'''<br>
+'''Hanna'''<br>
+<ul><li>'''P145''' left ITR</li>
+<ul><li>Primer: GATC_std_pQE-FP and GATC_std_m13-FP</li></ul>
+<li>'''P150''' right ITR</li>
+<ul><li>Primer: GATC_std_pQE-FP and GATC_std_m13-FP</li></ul>
+</ul>
+<br>
+'''Anissa'''<br>
+<ul><li>'''P136''' pSB1C3_hgh</li>
+<ul><li>Primer: O51_Reverse Primer (VR2)</li></ul>
+<li>'''P139''' pAAV_BamHI</li>
+<ul><li>Primer: O36_Rep_1250_rev</li></ul>
+<li>'''P143''' pAAV_RC_SalI</li>
+<ul><li>Primer: O53_Rep_1250_for</li></ul>
+<li>'''P141''' pGL3_QTERT</li>
+<ul><li>Primer: GATC_std_pTal-FP</li></ul>
+<li>'''P133''' pSB1C3_betaGlobin</li>
+<ul><li>Primer: O51_ReversePrimer (VR2)</li></ul>
+<li>'''P145''' pSB1C3_CMV</li>
+<ul><li>Primer: O51_ReversePrimer (VR2)</li></ul>
+</ul>
+<br>
+'''Jessica'''<br>
+<ul>
+<li>'''P129''' pSB1C3_SDM_PvuII</li>
+<ul>
+<li>Primer: GATC_std_pTeSp-2</li>
+</ul>
+</ul>
+<br>
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Preparation of competent E.coli</b></p>====
+'''Investigator: Jessica'''
+<ul><li>15ml DYT was prepared with 15µl tetracycline and inoculate with XL1B</li>
+<li>10ml DYT w/o antibiotics was prepared and inoculate with BL21 (just for glycerol stock, no competent cells)</li></ul><br>
+both were incubate over night in 37°C room
+<br>
+<br>
+====<p style="font-size:15px; background-color:#FF00FF;"><b>Last Mini-Prep and test digestion of ITRs</b></p>====
+'''Investigator: Hanna'''<br>
+<br>
+<p style="font-size:18px; font-weight: bold; color:#FF00FF;"><u>Plasmid Mini-Prep</u></p>
+*new vector name: pGA14_RFC10_leftITR and pGA14_RFC10_rightITR
+<br />
+<u><b>Glycerol Stocks</b></u> <br>
+<b>pGA14_RFC10_leftITR</b>
+{| border="1"
+| align="left" |  ||align="left"| '''Clone 1''' ||align="left"| '''Clone 2''' ||align="left"| '''Clone 3'''
+|-
+| align="left" | '''Bacteria strain''' ||align="left"| XL1blue ||align="left"| XL1blue  ||align="left"| XL1blue
+|-
+| align="left" | '''Plasmidname''' ||align="left"| pGA14_RFC10_leftITR ||align="left"| pGA14_RFC10_leftITR ||align="left"| pGA14_RFC10_leftITR
+|-
+| align="left" | '''Date''' ||align="left"| 2.8.10 ||align="left"| 2.8.10 ||align="left"| 2.8.10
 |-
-| align="left" | Clone||align="left"|1.3 + 1.4 ||align="left"|2.3 + 2.4 ||align="left"|4.3 + 4.4 ||align="left"|6.3 + 6.4 ||align="left"|9.3 + 9.4 ||align="left"|11.3 + 11.4||align="left"|12.2 + 12.4  ||align="left"| 13.2 + 13.4 ||align="left"| 14.3 + 14.4
+| align="left" | '''given glycerol-stock no.''' ||align="left"| B115 ||align="left"| B116 ||align="left"| B117
 |-
+| align="left" | '''given plasmid no.''' ||align="left"| P147 ||align="left"| P148 ||align="left"| P149
 |}
+<br>
+<b>pGA14_RFC10_rightITR</b>
+{| border="1"
+| align="left" |  ||align="left"| '''Clone 1''' ||align="left"| '''Clone 2''' ||align="left"| '''Clone 3'''
+|-
+| align="left" | '''Bacteria strain''' ||align="left"| XL1blue ||align="left"| XL1blue  ||align="left"| XL1blue
+|-
+| align="left" | '''Plasmidname''' ||align="left"| pGA14_RFC10_rightITR ||align="left"| pGA14_RFC10_rightITR ||align="left"| pGA14_RFC10_rightITR
+|-
+| align="left" | '''Date''' ||align="left"| 2.8.10 ||align="left"| 2.8.10 ||align="left"| 2.8.10
+|-
+| align="left" | '''given glycerol-stock no.''' ||align="left"| B112 ||align="left"| B113 ||align="left"| B114
+|-
+| align="left" | '''given plasmid no.''' ||align="left"| P150 ||align="left"| P151 ||align="left"| P152
+|}
+<br />
+<p style="font-size:15px; font-weight: bold; color:#FF00FF;">Test digestion</p>
+*buffer used: 4 ; Restriction-enzymes used: Enzyme 1 XbaI ; Enzyme 2 SpeI
+*Plasmid: pGA14_RFC10_leftITR:
+**Given Plasmid-Number: P147; DNA concentration: 240.22 ng/µL ;
+**Given Plasmid-Number: P148; DNA concentration: 268.97 ng/µL ;
+**Given Plasmid-Number: P149; DNA concentration: 234.16 ng/µL ;
+<br>
+*Plasmid: pGA14_RFC10_rightITR:
+**Given Plasmid-Number: P150; DNA concentration: 221.71 ng/µL ;
+**Given Plasmid-Number: P151; DNA concentration: 191.13 ng/µL ;
+**Given Plasmid-Number: P152; DNA concentration: 215.14 ng/µL ;
 <br />
-<p style="font-size:13px; color:#66bbff;"><b>
-Comment:</b> Samples 1.3, 2.3, 4.3, 6.3, 9.3, 11.3, 12.2, 13.2, 14.3 were sent for sequencing.  For sequencing results go to labday 02.09.10. </p>.
-====<p style="font-size:15px; background-color:#66bbff;"><b>Design of primers for pAAV_RC</b></p>====
+<br />
-<b>Investigator: Bea <br /></b>
+{| border="1"
-<p style="font-size:13px; color:#66bbff;">Primers for different cloning strategies of the synthesized cap gene into pAAV_Rc have been designed.</p>
+| align="left" | '''Components''' ||align="left"| <b>P147</b> Volume/µL ||align="left"| <b>P150</b> Volume/µL
-<ol>
+|-
-<li>The first primers are mutagenesis primers which delete the KpnI recognition site at position 3968. These primers can (or should be used) be used if cloning with BspMI/BfuI (isochizomer) does not cut the pAAV_RC efficiently. Instead of using this enzyme we can use XcmI to subclone the cap gene with performing a site-directed mutagenesis afterwards with designed primers. </li>
+| align="left" | DNA ||align="left"| 4.2 ||align="left"| 4.5
-<li>The second idea is to design oligoduplexes (hybridized oligos) which contain the recognition site for BspMI. In Gormley et al (2002) the idea was to add oligodupexes with the recognition site for BspMI and therefore provide the "second recognition site" in trans. </li>
+|-
-</ol>
+| align="left" | BSA (10x) ||align="left"| 1 ||align="left"| 1
-<b>Next step:</b> Check primers and order them today! Designed primers are stored in my Workingfolder under paav_rc and a word document was created whcih can be found under Oligos --> primers for different strategies...
+|-
-<br/>
+| align="left" | Buffer no. 4 (10x) ||align="left"| 1 ||align="left"| 1
+|-
+| align="left" | Enzyme 1 XbaI ||align="left"| 0.5 ||align="left"| 0.5
+|-
+| align="left" | Enzyme 2 SpeI ||align="left"| 0.5 ||align="left"| 0.5
+|-
+| align="left" | H<sub>2</sub>O ||align="left"| 2.8 ||align="left"| 2.5
+|-
+| align="left" | '''Total volume''' ||align="left"| <b>P147</b> ||align="left"| <b>P150</b>
+|}
+<br />
+*Incubation: 1 h
+<br />
+<p style="font-size:15px; font-weight: bold; color:#FF00FF;">Agarose-Gel:</p>
+<br />
+.83 g Agarose, 53 mL <b>TBE</b> (1.57%), 3 µL GELRED, at 115 Volt, running time: 45 minutes
+<br />
+<br />
+{| border="1" cellspacing="0" cellpadding="2" bordercolor="black"
+!Sample
+!Sample/µl]
+!Loading dye (5x)/µl
+!Expected size 1 (Geneious)
+!Expected size 2 (Geneious)
+|--
+|P147
+|10 µl
+|2 µl
+|157 bp
+|2902 bp
+|--
+|P150
+|10 µl
+|2 µl
+|156 bp
+|2903 bp
+|--
+|}
+{| align=right
+|}
+<br />
+*Marker: GeneRuler ladder mix
+{| border="1"
+|
+!Marker /µL
+!Sample P147 /µL
+!Sample P150 /µL
+|-
+!Lane
+|6.5
+|12
+|12
+|-
+|}
+<br />
+<br>
+<p style="font-size:15px; font-weight: bold; color:#FF00FF;">Test digestion delivered positive results for both ITRs: The expected fragment sizes (156 resp. 157 bp) could be detected in the referring range between the 100 and 200 bp marker nucleotides:</p> <br>
+[[File:LastITRPrep.jpg|400px]] <br>
+<br>
+<b>Comment:</b> In order to verify the results, P147 and P150 were sent for sequencing. Because sequencing never worked before, they will be sequenced under special conditions this time.<br>
+<br>
+====<p style="font-size:15px; background-color:#66bbff;">'''BioBrick production: mGMK in pSB1C3'''</p>====
+Investigator: Stefan<br>
+Backbone taken from: <br>
+*pSB1C3_CFP (P51.2): 151,1 ng/µl<br>
+Insert taken from: <br>
+*pAAV_RFC25_mGMK (P100): 411,3 ng/µl<br>
+{| border="1"
+| components   || align="right" |pSB1C3_CFP(P51.2) /µl|| align="right" |pAAV_RFC25_mGMK (P100) /µl
+|-
+| DNA  ||  align="right" |8 ||  align="right" | 5
+|-
+| BSA (10x) ||  align="right" |2||  align="right" | 2
+|-
+| Buffer 4 (10x)||  align="right" |2 ||  align="right" | 2
+|-
+|XbaI ||  align="right" |1 ||  align="right" | 1
+|-
+|AgeI ||  align="right" |1 ||  align="right" | 1
+|-
+|H<sub>2</sub>O||  align="right" |6 ||  align="right" | 9
+|-
+|'''Total volume '''||  align="right" |20 ||  align="right" | 20
+|}
+<br>
+* 1% Agarose gel
+* 3 µl Gelred
+*7 µl DNA-Ladder-Mix
+* 115 Volt, running time: 50 minutes
+Afer 50 minutes a picture (see below) was taken. Because there was no clear pattern (two bands) for the pSB1C3 backbone, the band of the insert mGMK was cut out and the gel ran another 20 minutes. After that, there were still two bands. Both were cut out and it was continued with two possible backbones. They were labeled vector (lower) and vector (upper).<br>
+[[File:Freiburg10 BioBrick pSB1C3 mGMK.jpg|400px|thumb|left|]]<br>
+<br />
+{| border="1"
+| '''Sample/µl ''' ||''' Expected size/bp
+|-
+| Vector pSB1C3  ||  align="right" |2082
+|-
+| Insert mGMK ||   align="right" |603
+|-
+|}
+<br />
+* weight of insert mGMK gel extract: 0,17 g
+* weight of vector (lower) pSB1C3 gel extract: 0,08 g
+* weight of vector (upper) pSB1C3 gel extract: 0,09 g
+'''Nanodrop'''
+* insert mGMK : 4,13 ng/µl
+* vector (lower) pSB1C: 5,47 ng/µl
+* vector (upper) pSB1C: 0,60 ng/µl => for calculation of ligation approach calculated with 1 ng/µl
+<br>
+'''Ligation'''
+*vector (lower) : insert - 4,16 µl : 4,84 µl
+*vector (upper) : insert - 7,43 µl : 1,57 µl<br>
+'''Transformation'''
+Two approaches were prepared, one for each vector and put in 37 °C room overnight.
+<br>
+<br>
+====<p style="font-size:15px; background-color:#FF00FF;"><b>Sequencing results of SDM Rep 68 & 78</b></p>====
+'''Investigator: Hanna and Volker'''<br>
+The sequencing results delivered that the PstI restriction sites of Rep 68 and Rep 78 were successfully deleted via side-directed mutageneis:
+<br>
+<gallery widths=500px heights=300px perrow=2 caption="Sequencing results of SDM Rep 68 & 78">
+File:Rep68.jpg |Rep 68
+File:Rep78.jpg |Rep 78
+</gallery>
+===78.Labortag 03.08.2010===
+====<p style="font-size:15px; background-color:#66bbff;">'''Results of sequencing pSB1C3_CFP_SDM_PvuII'''</p>====
+'''Investigator: Jessica'''<br>
+<b>SDM of PvuII:</b>
+[[File:PvuII.jpg|600px]]
+<br>
+<br>
+'''PvuII is succesfully deleted in the vector pSB1C3_RFC25_CFP'''
+<br>
+<br>
+====<p style="font-size:15px; background-color:#66bbff;">'''Repetition of the quickchange site-directed mutagenesis of pAAV_RC_1.1_SalI'''</p>====
+'''Investigator: Kerstin,Anissa'''<br>
+<p style="font-size:13px; color:#68bbff;">'''''Comments:''''' Sequenzing revealed no mutagenesis of SalI in pAAV_RC_1.1_SalI, so SDM now will be repeated.</p> <br>
+PCR-reaction:
+{| border="1"
+| '''Volume / µl''' || align="right" |'''ingredients'''|| align="right" |'''recommended /µl'''
+|-
+| 2,5  ||  align="right" |10X Pfu Ultra II buffer ||  align="right" | 2,5
+|-
+| 4,18 ||  align="right" |template (~10 ng)||  align="right" | 4,18 of 1:100 dilution
+|-
+| 0,58||  align="right" |forward primer: O68||  align="right" | 62,5 ng
+|-
+|0,58 ||  align="right" |reverse primer: O69 ||  align="right" | 62,5 ng
+|-
+|- ||  align="right" |DMSO ||  align="right" | -
+|-
+|0,5||  align="right" |dNTP||  align="right" | 250 µM each dNTP
+|-
+|16,16||  align="right" |H<sub>2</sub>O ||  align="right" |
+|-
+|0,5||  align="right" |PfuUltra II fusion (1.25) ||  align="right" |
+|}
+<br>
+PCR program:
+{| border="1"
+|'''Rounds'''|| align="right" |'''temperature/ °C'''|| align="right" |'''Time'''
+|-
+|1 ||  align="right" |95 ||  align="right" | 2 minutes
+|-
+| 20 ||  align="right" |95||  align="right" |30 seconds
+|-
+|20 ||  align="right" |80,4 ||  align="right" | 1 minute
+|-
+|20||  align="right" |68||  align="right" | 7,5 minutes
+|}
+<br>
+Plasmid was transformed into BL21 cells. Clones have to be picked tomorrow.
+<p style="font-size:13px; color:#ff0000;">'''''Comments:'''''NO CLONES, trafo didn't work, because annealing temperature was totally to high! (80,4 °C instead of 55°C) annealing temperature should always be 55°C (in case of troubleshooting temperature can be increased up to MAX. 68°C !)</p> <br>
+====<p style="font-size:15px; background-color:#66bbff;">'''PCR for Biobrickproduction of Rep 40, 52, 68, 78 and APP'''</p>====
+'''Investigators: Volker, Anna'''<br>
+Aim of the experiment:
+We wanted to produce biobricks from  the expression plasmids Rep40ex, Rep52 ex, the Rep 68 and 78 in which the PstI at position 310 was silenced and the AAP. This was performed by a PCR with primes that annealed to the ends of the later biobrick but also contained restriction sites that can be cut afterwards and cloned into pSB1C3.
+*Plasmids used as template:
+Rep_68_ex (p119):   c = 470,6 ng/µl <br>
+Rep_78_(p122):      c = 201,08 ng/µl <br>
+Rep_40_(p22.2):     c = 673,1 ng/µl <br>
+Rep_52_(p23.2):     c = 532,22 ng/µl <br>
+pAAV-RC containing AAP ORF (p50):    c = 378,5 ng/µl <br>
+*Primer used:
+For Rep_40_ex: Praefix_40_52_ex & Suffix_40_68_ex<br>
+For Rep_52_ex: Praefix_40_52_ex & Suffix_52_78_ex<br>
+For Rep_68_ex: Praefix_68_78_ex & Suffix_40_68_ex<br>
+For Rep_78_ex: Praefix_68_78_ex & Suffix_52_78_ex<br>
+For AAP_ex: Praefix_AAP_ex & Suffix_AAP_ex
+<br>
+*'''PCR:
+(was performed following the standard protocol)
+<br>
+{| border="1"
+| '''Ingredients''' || align="right" |'''Volume / µl''' || align="right" |'''Rep68'''|| align="right" |'''Rep78''' || align="right" |'''Rep40'''|| align="right" |'''Rep52'''|| align="right" |'''AAP'''
+|-
+| 5X Phusion HF buffer ||  align="right" |10 ||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" |
+|-
+| 10 mM dNTP mix||  align="right" |1||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" |
+|-
+| forward primer: ||  align="right" |2,5||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" |
+|-
+| reverse primer: ||  align="right" |2,5||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" |
+|-
+| DNA Template||  align="right" |***||  align="right" |4,2 µl ||  align="right" |1 µl ||  align="right" |2,9 µl||  align="right" |3,8 µl||  align="right" |5,3 µl
+|-
+|- DMSO (2%)||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" |
+|-
+| Phusion Polymerase||  align="right" |0,5||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" |
+|-
+|H<sub>2</sub>O||  align="right" |*** ||  align="right" | 28,3 µl||  align="right" | 31,5 µl||  align="right" | 29,6 µl||  align="right" | 28,7 µl||  align="right" |27,2 µl
+|-
+|Total volume||  align="right" |50
+|}
+<br>
+PCR program:
+{| border="1"
+|'''PCR Program'''|| align="right" |'''temperature/ °C'''|| align="right" |'''Time''' || align="right" |'''Rep40'''|| align="right" |'''Rep50'''|| align="right" |'''Rep68'''|| align="right" |'''Rep78'''|| align="right" |'''AAP'''
+|-
+|1||  align="right" |98 ||  align="right" |1min||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" |
+|-
+|2||  align="right" |98 ||  align="right" |15s||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" |
+|-
+|8x||  align="right" |*** ||  align="right" |25s||  align="right" |63°C||  align="right" |62°C||  align="right" |63°C||  align="right" |62°C||  align="right" |64°C
+|-
+|3 ||  align="right" |72||  align="right" |***||  align="right" |15s  ||  align="right" |18s||  align="right" |24s ||  align="right" |27s ||  align="right" | 10s
+|-
+|4 ||  align="right" |98||  align="right" | 15s||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" |
+|-
+|17x||  align="right" |***||  align="right" |25s||  align="right" |68°C||  align="right" |66°C||  align="right" |68°C||  align="right" |64°C||  align="right" |68°C
+|-
+|5||  align="right" |72||  align="right" |***||  align="right" |15s||  align="right" |18s||  align="right" |24s||  align="right" |27s||  align="right" |10s
+|-
+|6x||  align="right" |72||  align="right" |5min||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" |
+|-
+|Hold||  align="right" |4||  align="right" |  ||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" | ||  align="right" |
+|}
+<br>
+Five µl of PCR-product were used for an analytical gel to see if the PCR worked. <br>
+<gallery widths=500px heights=300px perrow=2 caption="BioBrick production for Rep and AAP">
+Image:Freiburg10_Biobrick-production for Rep40-78ex and  AAPex.jpg|Alalytical gel
+Image:Freiburg10_Biobrick-production for Rep40-78ex and  AAPex praeparative gel.jpg|Praeparative gel
+</gallery>
+<p style="color:red;">Comment: The result is that the PCR worked for the longer Rep proteins (68&78) with which a Quick-change was performed to remove the PstI(310) but not with the constructs for the smaller Rep variants (40&52) that were recieved from PD Kleinschmidt. As the longer Rep variants the AAP PCR Reaction also resulted in a PCR-product of the expected size. Unfortunately there were a secondary band of ~90bp for Rep_68_ex. For this reason we performed a praeparative gel and decided to cut the bands of all PCR products.</p> <br>
+The bands marked in the gel picture were cut and a gel extraction was performed.
+<p style="font-size:15px; font-weight: bold; color: blue;">Gel extraction</p>
+<br />
+Gel measurement:
+<br />
+{| border="1"
+| align="left" | '''Sample'''
+| align="left" | '''Weight'''
+| align="left" | '''Volume'''
+| align="left" | '''Concentration'''
+|-
+| align="left" | Rep_68_ex
+| align="left" | 0,1 g
+| align="left" | 20 µl
+| align="left" | 17,6 ng/µl
+|-
+| align="left" | Rep_78_ex
+| align="left" | 0,15g
+| align="left" | 20 µl
+| align="left" | 80,6 ng/µl
+|-
+| align="left" | AAP_ex
+| align="left" | 0,19 g
+| align="left" | 20µl
+| align="left" | 77,78 ng/µl
+|}<br>
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Continuation of preparation of competent E.coli</b></p>====
+'''Investigator: Jessica'''<br>
+preparation of competent XL1blue was finished according to the standard protocol
+<ul><li>aliquots of 60µl (to use for 1 trafo) are stored in -80°C freezer</li></ul>
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Sequencing of pSB1C3</b></p>====
+'''Investigator: Jessica'''<br>
+<p style="font-size:13px; color:#68bbff;">'''''Comments:''''' We sent for sequencing  '''pSB1C3_RFC25_longlinker (P105)''' to check the strange result of the test digestion of pSB1C3_SDM_PvuII(01.08.10. <br>
+pSB1C3_SDM_PvuII is too long for sequencing wherefore we sent pSB1C3_RFC25_longlinker because the longlinker just have 54kb (bp, nicht kb (Volker) (necessary is just the backbone we don't have.</p>
+<ul><li>Primer:</li>
+<ul>
+<li>RESgen-241698</li>
+<li>Reverse primer (VR2)</li>
+<li>o_F1-fw (from Gerrit)</li>
+</ul>
+</ul>
+<br>
+<br>
+====<p style="font-size:15px; background-color:#FF00FF;"><b>Design of Primer for p5 Promoter WT and TATA-less BioBrick production</b></p>====
+'''Investigator: Hanna'''<br>
+<br>
+[[File:Freiburg10 p5 Primer.JPG|500px|thumb|left|]]
+<br>
+[[File:Freiburg10 p5Primer Aim.JPG|500px|thumb|right|]]
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+===79.Labortag 04.08.2010===
+====<p style="font-size:15px; background-color:#66bbff;">'''Cloning of right ITR and left ITR into pSB1C3_RFC25_CFP'''</p>====
+Intention: Get biobricks ready. <br>
+Investigator: Patrick <br>
+pGA14_lITR_RFC10 (P147), pGA14_rightITR (P150) and pSB1C3_RFC25_CFP (P51.1) were digested with EcoRI and PstI (Buffer 4) according to the standard protocol. Digestion Time: 80 minutes.
+<br>
+GelRun: 1% Agarose Gel. Expected results (from left to right):
+*pSB1C3_RFC25_CFP: about 2100 bp and 800 bp.
+*pGA14_leftITR_RFC10: the size of the insert should be 135 bp.
+*pGA14_rightITR_RFC10: the size of the insert should be 138bp.
+[[File:20100704_patrick_bearbeitet.JPG|400px]]<br>
+<br>
+The mutual vector (now without CFP) and inserts (left ITR and right ITR) were cut out. The gelextraction was performed according to the standard protocol. DNA concentration of the extracts:
+* pSB1C3_RFC25_CFP: 2,9 ng/µl
+* left ITR: 1,4 ng/µl
+* right ITR: 2,0 ng/µl
+<br>
+The Quick Ligation was not performed according to the standard protocol:
+* left ITR + pSB1C3: 5µl Buffer, 1 µl Quick-Ligase, 2,5 µl left ITR, 1,5 µl pSB1C3_RFC25.
+* right ITR + pSB1C3: 5µl Buffer, 1 µl Quick-Ligase, 2,5 µl right ITR, 1,5 µl pSB1C3_RFC25.
+<br>
+Transformation: performed according to the standard protocol (BL21). The cells were plated on a agar plate with chloramphenicol. The clones will be picked tomorrow.
+<br>
+====<p style="font-size:15px; background-color:#66bbff;">'''Cloning of SDM SspI and SDM PvuII'''</p>====
+'''Investigator: Jessica'''
+*Vector: name: pSB1C3_SDM_SspI '''P125'''
+*Insert: name: pSB1C3_SDM_PvuII '''P129'''
+*new vector name: pSB1c3_SDM_SspI/PvuII '''P157'''
+*buffer used: 4 ; Restriction-enzymes used: Enzyme 1 (no. Lab: 141) BstI ; Enzyme 2 (no.Lab: 144) BpmI
+*DNA concentration (vector): 321,9 ng/µl ; DNA concentration (insert): 308,4 µg/µl
+<br />
+{| border="1"
+| '''components'''   || align="right" |'''volume of pSB1C3_SDM_SspI /µl''' || align="right" |'''volume of pSB1C3_SDm_PvuII /µl'''
+|-
+| DNA  ||  align="right" |4,66 ||  align="right" |4,87
+|-
+| BSA (10x) ||  align="right" |2 ||  align="right" | 2
+|-
+| Buffer 4 (10x)||  align="right" |2 ||  align="right" |2
+|-
+|Enzyme BstI (no.Lab:141)||  align="right" |1 ||  align="right" |1
+|-
+|Enzyme BpmI (no.Lab:144)||  align="right" |1 ||  align="right" |1
+|-
+|H2O||  align="right" |9,34 ||  align="right" |9,13
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 20||  align="right" |20
+|}
+<br />
+,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 130 Volt, running time:45
+<br />
+<br />
+<br />
+'''Loading plan for agarose gel''': <br>
+Marker used: GeneRuler ladder mix (Fermentas)<br>
+{| border="1"
+|
+!Marker
+!Sample 125, 20µl
+!Sample 129, 20µl
+|-
+!Lane
+|1
+|3
+|5
+|-
+|}
+<br>
+'''Results''': digesttemperature of BstI is 55°C, plasmid was just digested at 37°C... :( (<br>
+[[File:Digestion of SDM SspI and SDM PvuII.jpg|400px]] <br>
+====<p style="font-size:15px; background-color:#66bbff;">'''2nd Repetition of Quickchange site-directed mutagenesis of pAAV_RC_1.1_SalI'''</p>====
+'''Investigator: Kerstin, Anissa'''<br>
+<p style="font-size:13px; color:#68bbff;">'''''Comments:''''' Last trafo didn't work. Annealing temperature was to high (80,4°C instead of 55°C) </p> <br>
+Two approaches were made (short and long PCR:
+PCR-reaction:
+{| border="1"
+| '''Volume / µl''' || align="right" |'''ingredients'''|| align="right" |'''recommended /µl'''
+|-
+| 2,5  ||  align="right" |10X Pfu Ultra II buffer ||  align="right" | 2,5
+|-
+| 1,83 ||  align="right" |template (~10 ng): p139 (c: 546,97 ng/µl)||  align="right" | 1,83µl of 1:100 dilution
+|-
+| 0,58||  align="right" |forward primer: O68||  align="right" | 62,5 ng
+|-
+|0,58 ||  align="right" |reverse primer: O69 ||  align="right" | 62,5 ng
+|-
+|- ||  align="right" |DMSO ||  align="right" | -
+|-
+|0,5||  align="right" |dNTP||  align="right" | 250 µM each dNTP
+|-
+|18,51||  align="right" |H<sub>2</sub>O ||  align="right" |
+|-
+|0,5||  align="right" |PfuUltra II fusion (1.25) ||  align="right" |
+|}
+<br>
+PCR program (long):
+{| border="1"
+|'''Cycles'''|| align="right" |'''temperature/ °C'''|| align="right" |'''Time'''
+|-
+|1 ||  align="right" |95 ||  align="right" | 2 minutes
+|-
+| 20 ||  align="right" |95||  align="right" |30 seconds
+|-
+|20 ||  align="right" |55 ||  align="right" | 1 minute
+|-
+|20||  align="right" |68||  align="right" | 7,5 minutes
+|}
+<br>
+PCR program (short):
+{| border="1"
+|'''Cycles'''|| align="right" |'''temperature/ °C'''|| align="right" |'''Time'''
+|-
+|1 ||  align="right" |95 ||  align="right" | 2 minutes
+|-
+| 20 ||  align="right" |95||  align="right" |30 seconds
+|-
+|20 ||  align="right" |55 ||  align="right" | 1 minute
+|-
+|20||  align="right" |68||  align="right" | 4 minutes
+|}
+Plasmids were transformed into BL21 cells. Clones have to be picked tomorrow.
+====<p style="font-size:15px; background-color:#66bbff;"><b>Mini-Prep of pSB1C3_mGMK</b></p>====
+<b>Investigator: Chris W., Bea</b><br>
+Vector name: pSB1C3_mGMK upper band 1.1 and pSB1C3_mGMK upper band 1.2 and pSB1C3_mGMK lower band 2.1 and pSB1C3_mGMK lower band 2.2
+Mini-Prep following the standart Protokoll
+<br />
+<li>P153 = pSB1C3_mGMK upper band 1.1 = 248,3 ng/µl
+<li>P154 = pSB1C3_mGMK upper band 1.2 = 251,6 ng/µl
+<li>P155 = pSB1C3_mGMK lower band 1.1 = 263 ng/µl
+<li>P156 = pSB1C3_mGMK lower band 1.2 = 235,2 ng/µl
+<br />
+<br>
+<br>
+<b>Test digestion:</b>
+<ul>
+<li>Perfomed with 15 µL of total volume with all four clones</li>
+<table border=1 cellpadding=0 cellspacing=0 width=621 style='border-collapse:
+ collapse;table-layout:fixed;width:466pt'>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt'>
+  <td height=29 class=xl6724191 width=143 style='height:21.75pt;width:107pt'>&nbsp;</td>
+  <td class=xl6824191 width=131 style='border-left:none;width:98pt'>Mastermix/µL</td>
+  <td class=xl6824191 width=87 style='border-left:none;width:65pt'>P153/µL</td>
+  <td class=xl6824191 width=84 style='border-left:none;width:63pt'>P154/µL</td>
+  <td class=xl6824191 width=90 style='border-left:none;width:68pt'>P155/µL</td>
+  <td class=xl6824191 width=86 style='border-left:none;width:65pt'>P156/µL</td>
+ </tr>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt'>
+  <td height=29 class=xl6624191 width=143 style='height:21.75pt;border-top:
+  none;width:107pt'><span lang=EN-US style='mso-ansi-language:EN-US'>DNA</span></td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>-</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>3,5</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>3,5</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>3,5</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>3,5</td>
+ </tr>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt;mso-yfti-irow:
+'>
+  <td height=29 class=xl6624191 width=143 style='height:21.75pt;border-top:
+  none;width:107pt'><span lang=EN-US style='mso-ansi-language:EN-US'>BSA (10x)</span></td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>7,5</td>
+  <td rowspan=4 class=xl6524191 style='border-top:none'>4</td>
+  <td rowspan=4 class=xl6524191 style='border-top:none'>4</td>
+  <td rowspan=4 class=xl6524191 style='border-top:none'>4</td>
+  <td rowspan=4 class=xl6524191 style='border-top:none'>4</td>
+ </tr>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt;mso-yfti-irow:
+'>
+  <td height=29 class=xl6624191 width=143 style='height:21.75pt;border-top:
+  none;width:107pt'><span lang=EN-US style='mso-ansi-language:EN-US'>Buffer
+<span style='mso-spacerun:yes'>   </span>(10x)</span></td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>7,5</td>
+ </tr>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt;mso-yfti-irow:
+'>
+  <td height=29 class=xl6624191 width=143 style='height:21.75pt;border-top:
+  none;width:107pt'><span lang=EN-US style='mso-ansi-language:EN-US'>Enzyme
+  XbaI<span style='mso-spacerun:yes'> </span></span></td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>2,5</td>
+ </tr>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt;mso-yfti-irow:
+'>
+  <td height=29 class=xl6624191 width=143 style='height:21.75pt;border-top:
+  none;width:107pt'><span lang=EN-US style='mso-ansi-language:EN-US'>Enzyme
+  AgeI</span></td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>2,5</td>
+ </tr>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt;mso-yfti-irow:
+;mso-yfti-lastrow:yes'>
+  <td height=29 class=xl6624191 width=143 style='height:21.75pt;border-top:
+  none;width:107pt'><span lang=EN-US style='mso-ansi-language:EN-US'>H2O</span></td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>-</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>7,5</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>7,5</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>7,5</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>7,5</td>
+ </tr>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt'>
+  <td height=29 class=xl6624191 width=143 style='height:21.75pt;border-top:
+  none;width:107pt'>Total volume</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>15</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>15</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>15</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>15</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>15</td>
+ </tr>
+ <tr height=0 style='display:none'>
+  <td width=143 style='width:107pt'></td>
+  <td width=131 style='width:98pt'></td>
+  <td width=87 style='width:65pt'></td>
+  <td width=84 style='width:63pt'></td>
+  <td width=90 style='width:68pt'></td>
+  <td width=86 style='width:65pt'></td>
+ </tr>
+</table>
+<br />
+</ul>
+<ul>
+<li>All four samples were loaded on a 1% agarose gel</li>
+<li>P153 = pSB1C3_mGMK upper band 1.1 </li>
+<li>P154 = pSB1C3_mGMK upper band 1.2 </li>
+<li>P155 = pSB1C3_mGMK lower band 1.1</li>
+<li>P156 = pSB1C3_mGMK lower band 1.2</li>
+</ul>
+<br />
+[[File:Freiburg10 04 08 2010 Test digestion of pSB1C3 mGMK.jpg|400px]]
+<br />
+<br />
+<br />
+<b> Sequencing</b>:
+<ul>
+<li> Plasmid used: P156: pSB1C3_mGMK lower band 1.2</li>
+<li> Primer used: VR-2</li>
+<li> Tube name: Bea_1</li>
+</ul>
+====<p style="font-size:15px; background-color:#66bbff;">''' cell culture '''</p>====
+Investigator: Adrian
+<br />
+<b> Plan for the next virus production procedures </b>
+<br />
+The Motivation: investigation of the influence of different GOI amounts.
+<br />
+The Plan: keep rep/cap and pHelper amount stable (3,3 µg each => 6,6 µg), differ the GOI (YFP) amount in each stock.
+<br />
+Viral Stocks:
+* 3,3 µg YFP + 3,3 µg pHelper + 3,3  rep/cap
+* 10 µg YFP + 3,3 µg pHelper + 3,3  rep/cap
+* 20 µg YFP + 3,3 µg pHelper + 3,3  rep/cap
+<br />
+*3,3 µg pHelper + 3,3  rep/cap (<b>without GOI !!!</b>)
+<br />
+*one GMK_TK clone (with the confirmed sequence) + 3,3 µg pHelper + 3,3  rep/cap
+<br />
+<b>Transduction plan</b>
+<li>five 6-well-plates wille be transduced
+{| align=right
+|}
+{| border="1"
+|A
+!150µl AAV stock 1
+!300µl AAV stock 1
+!control no Virus
+|-
+!B
+|150µl AAV stock 2
+|300µl AAV stock 2
+|150µl AAV without GOI
+|-
+|}
+====<p style="font-size:15px; background-color:#66bbff;">'''Repetition of cloning of SDM SspI and SDM PvuII'''</p>====
+'''Investigator: Jessica'''
+*Vector: name: pSB1C3_SDM_SspI '''P125'''
+*Insert: name: pSB1C3_SDM_PvuII '''P129'''
+*new vector name: pSB1C3_RFC25_SDM_SspI/PvuII '''P157'''
+*buffer used: 4 ; Restriction-enzymes used: Enzyme 1 (no. Lab: 141) BtsI ; Enzyme 2 (no.Lab: 144) BpmI
+*DNA concentration (vector): 321,9 ng/µl ; DNA concentration (insert): 308,4 µg/µl
+<br />
+{| border="1"
+| '''components'''   || align="right" |'''volume of pSB1C3_SDM_SspI /µl''' || align="right" |'''volume of pSB1C3_SDm_PvuII /µl'''
+|-
+| DNA  ||  align="right" |4,66 ||  align="right" |4,87
+|-
+| BSA (10x) ||  align="right" |2 ||  align="right" | 2
+|-
+| Buffer 4 (10x)||  align="right" |2 ||  align="right" |2
+|-
+|Enzyme ClaI (no.Lab:152)||  align="right" |1 ||  align="right" |1
+|-
+|Enzyme BpmI (no.Lab:144)||  align="right" |1 ||  align="right" |1
+|-
+|H2O||  align="right" |9,34 ||  align="right" |9,13
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 20||  align="right" |20
+|}
+incubation time: 1,5h
+<br />
+,5 g Agarose,50 ml TBE (1%), 3 µl GELRED (gel was shared with Anna) , at  Volt, running time:
+<br />
+<br />
+<br />
+'''Loading plan for agarose gel''': <br>
+Marker used: GeneRuler ladder mix (Fermentas)<br>
+{| border="1"
+|
+!Marker
+!Sample 125, 20µl
+!Sample 129, 20µl
+|-
+!Lane
+|1
+|3
+|5
+|-
+|}
+This appproach also didn't work, same result. the guess is that BpmI doesn't work anymore. will be repeated by Chris W. on 05.08.10. the result will show that the guess is right and BpmI from labstock is changed out with a new one.
+====<p style="font-size:15px; background-color:#66bbff;">'''Test transformation of XL1 competent cells'''</p>====
+Investigator: Kira
+Test transformation was performed in order to test the efficiency of produced chemical competent XL1 blue cells.
+plates were prepared: one with 50 pg and the second with 100 pg pUC 18 plasmid (50 pg/㎕)
+pg plate: 1 ㎕ pUC + 50 ㎕ XL1B cells
+pg plate: 2 ㎕ pUC + 50 ㎕ XL1B cells
+Transformation was performed according to the standard protocol and the plates were incubated at 37 C.
 <br/>
-====<p style="font-size:15px; background-color:#ff00ff;"><b>Sequencing results of pSB1C3_Zegfr:1907_Linker</b></p>====
+====<p style="font-size:15px; background-color:#ff00ff;">'''Sequencing results of ITRs'''</p>====
-<b>Investigator: Hanna<br /></b>
+Investigator: <b>Hanna</b>
 <br/>
+sequencing files were analyzed "per hand" base by base. Alignments (will be inserted soon) delivered that the right ITR is 100% OK and was successfully converted into the RFC10 BioBrick standard. <br/>
-<p><font color="#00ff00;"><b>Comment:</b> Sequencing results looked all well. One bp was missing in the theoretical sequence of SEG suffix - but is correct in the actual sequence.</font></p>
+[[File:Freiburg10_Sequencing_RFC10RightITR_2.jpg]] <br/>
+The sequencing and alignments of the left ITR delivered that a 15 bp fragment in the middle of the sequence is lacking. Therefore further test digestions have to be performed. Nevertheless also this ITR was successfully converted into the RFC10 BioBrick standard. Secondary structure analysis showed that the stemloop-structure will be nevertheless forming. We will try to test whether the referring fragment is also missing in the pAAV_MCS. If it's also lacking there we will continue with this ITR and test whether it functions.
 <br/>
-<b><u>pSB1Cr_Zegfr:1907_LongLinker:</u></b> <br/>
+[[File:Freiburg10 Sequencing RFC10LeftITR 2.jpg]]
-[[File:PSB1C3 Zegfr1907 LongLinker.JPG|700px]]
 <br/>
-<b><u>pSB1Cr_Zegfr:1907_SEG:</u></b><br/>
-[[File:PSB1C3 Zegfr1907 SEG.JPG|700px]]
 <br/>
-<b><u>pSB1Cr_Zegfr:1907_MiddleLinker:</u></b><br/>
+====<p style="font-size:15px; background-color:#66bbff;">'''Cloning of Rep68, Rep78 and AAP into pSB1C3'''</p>====
-[[File:PSB1C3 Zegfr1907 MiddleLinker.JPG|700px]]
+'''Investigator: Anna
-<br/>
-<b><u>pSB1Cr_Zegfr:1907_ShortLinker:</u></b><br/>
+<p style="font-size:13px; color:#68bbff;">'''''Comments''''': The PCR of Rep 40/52 didn't work (see 03.08), whereas the PCR of Rep 68/78 and AAP was succesful. Ligation was done with two different samples of pSB1C3 (see agarose gel). Samples from digestion and from ligation are stored in the 4°C freezer.</p> <br>
-[[File:PSB1C3 Zegfr1907 ShortLinker.JPG|700px]]
-<br/>
+*Digestion of PCR products and vector:
-These constructs will be cloned into pCerulean for N-terminal fusion to VP2.
-<!--insert this text wherever you want. copy from here until "STOP"-->
-<html>
 <br />
-<a href="#top">go to the top ;)</a>
+{| border="1"
-</html>
+| '''components'''   || align="right" |'''PCR product /µl''' || align="right" |'''vector /µl'''
-<!--"STOP"-->
+|-
-====<p style="font-size:15px; background-color:#66bbff;"><b>Trafo evalutaion and Inoculation</b></p>====
+| DNA  ||  align="right" |19 ||  align="right" |10
-<b>Investigator: Kira</b>
+|-
-<br/>
+| BSA (10x) ||  align="right" |3 ||  align="right" | 3
-The plate with transformed CD-biobrick contains around 40 colonies. 4 of them will be inoculated into LB and incubated @37 C over-night.
+|-
-<!--insert this text wherever you want. copy from here until "STOP"-->
+| Buffer 4 (10x)||  align="right" |3 ||  align="right" |3
-<html>
+|-
+|Enzyme '''XbaI ||  align="right" |1 ||  align="right" |1
+|-
+|Enzyme '''SpeI ||  align="right" |1 ||  align="right" |1
+|-
+|H2O||  align="right" |3 ||  align="right" |12
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 30||  align="right" |30
+|}
 <br />
-<a href="#top">go to the top ;)</a>
+<p style="font-size:13px; color:#68bbff;">'''''Comments''''': Digestion was done with XbaI and SpeI, it has to be checked if the inserts are cloned into the vector in the right orientation. </p> <br>
-</html>
-<!--"STOP"-->
-====<p style="font-size:15px; background-color:#66bbff;"><b>Continuation: Cloning CFP_middlelinker (from pSB1C3_CFP_middlelinker, P276) into pCerulean (P273)</b></p>====
+*Purification of Rep68, 78 and AAP:
+For the purification 95 µl of buffer PBI was used.
-<b>Investigator: Patrick</b>
+c(Rep68)= 17,6 ng/µl <br />
+c(Rep78)= 80,60 ng/µl <br />
+c(AAP)= 77,78 ng/µl
+<br />
-The two Ligations were performed according to the standard protocol:<br>
+*Gelextraction of pSB1C3_RFC25_CFP:
-µl T4 DNA ligase, 1 µl 10x Buffer, 4,6 µl vector (P273), 3,34 µl Insert (P276, upper and lower band).<br>
+,5 g Agarose,50 ml TBE (1%), 3 µl GELRED , at 115 Volt, running time:55 <br />
-Incubation time: 50 minutes.
+µl loading dye (6x) for the sample, Marker: GeneRuler ladder mix (Fermentas)
+<br />
+<br />
+<br />
+<br />
-During the transformation i forgot to put the cells into the 37°C shaker so i incubated them afterwards again for 45 minutes at 37 °C on a shaker.
+[[file:Digestion of pSB1C3.jpg]]
+<br />
-The mutual conles will be picked tomorrow to inoculate 10 ml DYT following a mini-prep on 03.09.2010
-====<p style="font-size:15px; background-color:#66bbff;"><b>Transfection, Seeding AAV293 and HT1080</b></p>====
+c(pSB1C3)= 2,87 ng/µl <br />
-<b> Investigator: Kerstin </b>
+c(pSB1C3_2)= 9,46 ng/µl
-*Transfection: 10 plates, same treatment (10µg of RC (P357), pHelper (P356)and mVenus (P263), following the standard protocol)
+<br />
-*Seeding HT1080 for transduction with virus from 21.08.2010 (10µg of RC, pHelper, TKGMK; pH=7,10)
-*Seeding AAV293 for transfection with plasmids without HgH or beta-globin (verifying functionality)
-====<p style="font-size:15px; background-color:#66bbff;"><b>Cloning of Z<sub>EGFR</sub>:1907_Middle-Linker,Z<sub>EGFR</sub>:1907_Short-Linker, Z<sub>EGFR</sub>:1907_SEG-Linker and Z<sub>EGFR</sub>:1907_Long-Linker into pCerulean</b></p>====
+*Quickligation of PCR products and vector:
-<b>Investigator: Stefan </b>
-<p style="font-size:13px; color:red;"><b>Comment</b>:</p>
+For the Ligation 10µl buffer (2x) and 1µl Quickligase were used.
+<br />
+{| border="1"
+| ''' '''   || align="right" |'''Sample-no.'''|| align="right" |'''vector /µl''' || align="right" |'''insert /µl'''
+|-
+| pSB1C3 + Rep68 ||  align="right" |1.1 || align="right" |6,51 ||  align="right" |2,4
+|-
+| pSB1C3_2 + Rep68 ||  align="right" |1.2 ||  align="right" |3,9 ||  align="right" | 5,02
+|-
+| pSB1C32 + Rep78 ||  align="right" |2.1 || align="right" |8,2 ||  align="right" |0,8
+|-
+| pSB1C3_2 + Rep78 ||  align="right" |2.2 ||  align="right" |6,82 ||  align="right" |2,18
+|-
+| pSB1C3 + AAP ||  align="right" |3.1 ||  align="right" |8,71 ||  align="right" |0,92
+|-
+| pSB1C3_2 + AAP  ||  align="right" |3.2 ||  align="right" |8,1 ||  align="right" |0,9
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 9||  align="right" | ||  align="right" |
+|}
+<br />
+*Transformation:
+The transformation was done following the standard protocol using B21 cells.
+===80.Labortag 05.08.2010===
+====<p style="font-size:15px; background-color:#66bbff;"><b>New LB Agar was prepared.</b></p>====
+Investigator: Patrick
+====<p style="font-size:15px; background-color:#66bbff;"><b>Sequenc analysis of BioBricks: CMV, hGH and beta globin</b></p>====
+<b>Investigator: Bea</b><br />
+<p style="font-size:13px; color:#68bbff;"><b>Comments</b>: Sequence analysis of three BioBricks which were cloned into the iGEM standard plasmid pSB1C3. Cloning of this three plasmids were performed at: </p> <br/ >
+<ul>
+<li>  </li>
+<li>   </li>
+<li>   </li>
+</ul>
+<p style="font-size:13px; color:#b2222;"><b>Sequencing results of pSB1C3_CMV: </b></p>
+<br />
+<ul>
+<li>Plasmid sent for sequencing: </li>
+<li>Primer used: VR-2 </li>
+<li><b>Results:</b> Sequence read looks good. The incorporation of the PCR product can be confirmed. It can be seen that the insert is in the RFC10 standard and prefix and suffix have the right sequence. Therefore, this BioBrick can be send to the registry and used for BioBrick assembly.But: there is a mutation in the termintor (sequence picture do not show this mutation)</li>
+</ul>
+<img src="http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/images/7/74/Freiburg10_Sequence_analysis_of_PSB1C3_CMV.jpg" />
+<br />
+<p style="font-size:13px; color:#b2222;"><b>Sequencing results of pSB1C3_hGH: </b></p>
+<br />
+<ul>
+<li>Plasmid sent for sequencing: </li>
+<li>Primer used: VR-2 </li>
+<li><b>Results:</b> Sequence read looks good. The incorporation of the PCR product can be confirmed. It can be seen that the insert is in the RFC10 standard and prefix and suffix have the right sequence. Therefore, this BioBrick can be send to the registry and used for BioBrick assembly.</li>
+</ul>
+http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/images/e/e1/Freiburg10_Sequence_analysis_of_PSB1C3_betaglobin.jpg
+<br />
+<p style="font-size:13px; color:#b2222;"><b>Sequencing results of pSB1C3_hGH: </b></p>
+<br />
+<ul>
+<li>Plasmid sent for sequencing: </li>
+<li>Primer used: VR-2 </li>
+<li><b>Results:</b> Sequence read looks good. The incorporation of the PCR product can be confirmed. It can be seen that the insert is in the RFC10 standard and prefix and suffix have the right sequence. Therefore, this BioBrick can be send to the registry and used for BioBrick assembly.</li>
+</ul>
+http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/images/4/44/Freiburg10_Sequence_analysis_of_PSB1C3_hGH.jpg
+====<p style="font-size:15px; background-color:#66bbff;"><b> Cellculture </b></p>====
+Investigator: Adrian<br />
+<br />
+<br />
+The Motivation: Transfection<br />
+The Action: HEK cells were split into four T75 flasks<br />
+The Plan: The cells should be ready at saturday for seeding and monday for transfection<br />
+<br /><br />
+We recived new HT1080 cells, they'll be split tomorrow (thx to Sven)
+<br /><br />
+We recived new tumor cells which overexpress EGFR (thx to barbara)
+====<p style="font-size:15px; background-color:#66bbff;"><b>Picking clones of pSB1C3_AAP_2, pSB1C3_AAP, pSB1C3_Rep78_2, pSB1C3_Rep78, pSB1C3_Rep68_2 and pSB1C3_Rep68</b></p>====
 <br/>
-'''Digestion:'''
+Investigator: Anissa
+<br/>
+Of each construct two clones were picked. plates are still stored in the cold-room, tomorrow mini-prep will be done.
+<br />
+====<p style="font-size:15px; background-color:#66bbff;"><b>PCR and ligation for biobrick-production of pSB1C3_hTERT</b></p>====
+<br/>
+Investigator: Anissa,Kerstin<br />
+<br />
+<br />
+<p style="font-size:13px; color:#68bbff;">'''''Comments''''': PCR was performed one time without DMSO and one time with DMSO. Only the approach with DMSO showed bands in the analytic gel after PCR. That's why only this approach will be noted. </p> <br>
+<br>
+*'''PCR:
+(was performed following the standard protocol)
+<br>
 {| border="1"
-| components   || align="right" |Vector (P273) || align="right" |Z<sub>EGFR</sub>:1907_Middle-Linker (P290) || align="right" |Z<sub>EGFR</sub>:1907_Short-Linker (P292) || align="right" |Z<sub>EGFR</sub>:1907_SEG-Linker (P296) || align="right" |Z<sub>EGFR</sub>:1907_Long-Linker (P298)
+| '''Ingredients''' || align="right" |'''Volume / µl'''
 |-
-| DNA  ||  align="right" |3,8 ||  align="right" | 8,8 ||  align="right" | 10,2 ||  align="right" | 9,2 ||  align="right" | 8,7
+| 5X Phusion HF buffer ||  align="right" |10
 |-
-| BSA (10x) ||  align="right" |2||  align="right" | 2||  align="right" | 2||  align="right" | 2||  align="right" | 2
+| 10 mM dNTP mix||  align="right" |1
 |-
-| Buffer 4 (10x)||  align="right" |2 ||  align="right" | 2 ||  align="right" | 2||  align="right" | 2||  align="right" | 2
+| forward primer: O111 (phTERT_prefix_for_RFC10) ||  align="right" |2,5
 |-
-|XbaI ||  align="right" |1 ||  align="right" |1||  align="right" |1||  align="right" |1||  align="right" |1
+| reverse primer: O112 (phTERT_suffix_rev_RFC10) ||  align="right" |2,5
 |-
-|PstI  ||  align="right" |1||  align="right" |1||  align="right" |1||  align="right" |1||  align="right" |1
+| DNA Template||  align="right" |0,35 µl
 |-
-|H<sub>2</sub>O||  align="right" |10,2 ||  align="right" | 5,2||  align="right" | 3,8||  align="right" | 4,8||  align="right" | 5,3
+| DMSO (2%)||  align="right" | 1
 |-
-|'''Total volume '''||  align="right" |20||  align="right" | 20||  align="right" | 20||  align="right" | 20||  align="right" | 20
+| Phusion Polymerase||  align="right" |0,5
+|-
+|H<sub>2</sub>O||  align="right" |32,15
+|-
+|Total volume||  align="right" |50
 |}
 <br>
-,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 115 Volt, running time: 50 minutes
+PCR program:
+{| border="1"
+|'''PCR Program'''|| align="right" |'''temperature/ °C'''
+|-
+|1||  align="right" |98
+|-
+|2||  align="right" |98
+|-
+|8x||  align="right" |58
+|-
+|3 ||  align="right" |72
+|-
+|4 ||  align="right" |98
+|-
+|17x||  align="right" |70
+|-
+|5||  align="right" |72
+|-
+|6x||  align="right" |72
+|-
+|Hold||  align="right" |4
+|}
+<br>
+<gallery widths=500px heights=300px perrow=2 caption="BioBrick production of pSB1C3_hTERT">
+Image:Freiburg10_pSB1C3 cut with XbaI and PstI for TERT promoter.jpg|Preparative gel
+Image:Freiburg10_hTERT after PCR.jpg|analytic gel
+</gallery>
+<br/>
+<p style="font-size:15px; font-weight: bold; color: blue;">Gel extraction</p>
 <br />
+Gel measurement:
 <br />
+{| border="1"
+| align="left" | '''Sample'''
+| align="left" | '''Weight'''
+| align="left" | '''Volume'''
+| align="left" | '''Concentration'''
+|-
+| align="left" | hTERT
+| align="left" | 0,15g
+| align="left" | 20 µl
+| align="left" | 37,49 ng/µl
+|-
+| align="left" | pSB1C3_cut
+| align="left" | 0,08g
+| align="left" | 20 µl
+| align="left" | 4,56 ng/µl
+|}
+<br>
+*Digestion of PCR product and vector:
 <br />
+{| border="1"
+| '''components'''   || align="right" |'''PCR product /µl''' || align="right" |'''vector /µl'''
+|-
+| DNA  ||  align="right" |18||  align="right" |7,58
+|-
+| BSA (10x) ||  align="right" |0,3 (100X used)||  align="right" | 2
+|-
+| Buffer 4 (10x)||  align="right" |2,5 ||  align="right" |2
+|-
+|Enzyme '''XbaI ||  align="right" |1 ||  align="right" |1
+|-
+|Enzyme '''PstI ||  align="right" |1 ||  align="right" |1
+|-
+|H2O||  align="right" |2,2 ||  align="right" |6,42
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 25||  align="right" |20
+|}
 <br />
-[[File:Freiburg10 pCerulean affi linker.jpg|500px|]]
+Ligation with T4-Ligase and transformation with BL 21 was made. Clones have to be picked tomorrow.
+====<p style="font-size:15px; background-color:#66bbff;"><b>Transformation evaluation of XL1B cells and repetition of transformation</b></p>====
+Investigator: Kira <br />
+Against our expectations both agar plates contain very few colonies. In order to figure out if the lack of colonies is due to the XL1 blue cells or loss of pUC activity, test transformation will be repeated this evening with recently prepared XL1 blue cells as well as with Lab-XL1B cells.
+pg pUC-plate contains 8 colonies
+pg pUC-plate contains 18 colonies
+Transformation will be performed again with 100 pg pUC (= 2 ㎕ pUC).
 <br />
+====<p style="font-size:15px; background-color:#66bbff;">'''Cloning of SDM SspI and SDM PvuII'''</p>====
+'''Investigator: Chris W.'''
+*Vector: name: pSB1C3_SDM_SspI '''P125'''
+*Insert: name: pSB1C3_SDM_PvuII '''P129'''
+*new vector name: pSB1c3_SDM_SspI/PvuII '''P157'''
+*buffer used: 4 ; Restriction-enzymes used: Enzyme 1 (no. Lab: 144) BpmI ; Enzyme 2 (no.Lab: 152) ClaI
+*DNA concentration (vector): 321,9 ng/µl ; DNA concentration (insert): 308,4 µg/µl
 <br />
+{| border="1"
+| '''components'''   || align="right" |'''volume of pSB1C3_SDM_SspI /µl''' || align="right" |'''volume of pSB1C3_SDm_PvuII /µl'''
+|-
+| DNA  ||  align="right" |4,66 ||  align="right" |4,87
+|-
+| BSA (10x) ||  align="right" |2 ||  align="right" | 2
+|-
+| Buffer 4 (10x)||  align="right" |2 ||  align="right" |2
+|-
+|Enzyme BpmI (no.Lab:144)||  align="right" |1 ||  align="right" |1
+|-
+|Enzyme ClaI (no.Lab:152)||  align="right" |1 ||  align="right" |1
+|-
+|H2O||  align="right" |9,34 ||  align="right" |9,13
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 20||  align="right" |20
+|}
+<br> <p style="color:red;">Comment: I guess enzyme 144 was BpmI and enzyme 152 was ClaI ? (Jessica)</p> <br>
+<br> <p style="color:red;">Comment: u r right, changed (Chris)</p> <br>
 <br />
+,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 130 Volt, running time:45
 <br />
 <br />
-'''Gelextraction:'''<br />
+<br />
+'''Loading plan for agarose gel''': <br>
+Marker used: GeneRuler ladder mix (Fermentas)<br>
-The gelextraction was performed according to the standard protocol. DNA concentration of the extracts:
+{| border="1"
-* P273: c= 3,1 ng/µl
+|
-* P290: c= 3,2 ng/µl
+!Marker
-* P292: c= 1,8 ng/µl
+!Sample 125, 20µl
-* P296: c= 3,0 ng/µl
+!Sample 129, 20µl
-* P298: c= 3,2 ng/µl
+|-
+!Lane
+|1
+|5
+|7
+|-
+|}
+<br>
+[[File:Gel1.png|500px|left|thumb|]]
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
 <br>
-'''T4 Ligation:'''<br />
-The  Ligation was performed as following:<br />
-<p style="font-size:13px; color:red;"><b>Comment</b>: No sufficent vector concentration, therefore 5 µl of vector was used for every approach. </p>
-* Vector Volume: 5 µl
-* Insert Volume: 3 µl
+The mutual vector (now without SspI) and insert (now without PvuII) were cut out. The gelextraction was performed according to the standard protocol. DNA concentration of the extracts:
+* P125 Sspl: 12,8 ng/µl
+* P129 PvuII: 11,6 ng/µl
+<br>
+The  Ligation was performed as following:
+* Vector Volume: 2,81 µl
+* Insert Volume: 5,19 µl
 <br>
 * 1µl T4-Ligase buffer (10x)
 * 8µl (Vector + Insert) mix
 * 1µl T4-Ligase
-<br> Incubating for 40 minutes.
+<br> Incubate for 30min
 <br>
-'''Transformation:'''<br />
+'''Transformation:''' performed according to the standard protocol (BL21). The cells were plated on a agar plate with chloramphenicol
-Trafo was performed according to the standard protocol (BL21). The cells were plated on a agar plate with chloramphenicol
 <br>
+====<p style="font-size:15px; background-color:#66bbff;"><b>Miniprep of p158 and p159</b></p>====
+<p style="font-size:20px; font-weight: bold; color: blue;"><u>Plasmid Mini-Prep</u></p>
+Investigator: Bea & Volker<br>
+For the tripple mutant of pAAV-RC a Quick-change reaction was carried out to remove the last restriction site (SalI) that is required for the Viral Brick standard. For this construct glycerol stocks and minipreps were carried out for two clones.<br>
-===108. labday 02.09.2010===
-====<p style="font-size:15px; background-color:#66bbff;"><b>Sequencing of loop insertions BioBricks: 2nd round</b></p>====
-<b>Investigator: Achim, Anna <br /></b>
 <br />
-We analyzed the new sequencing results and found two correct sequences:
+<u>Glycerol Stocks</u>
+{| border="1"
+| align="left" |  ||align="left"| '''Clone 1''' ||align="left"| '''Clone 2'''
+|-
+| align="left" | '''Bacteria strain''' ||align="left"| BL-21 ||align="left"| BL-21
+|-
+| align="left" | '''Plasmidname''' ||align="left"| pAAV_RC_1.2 SDM SalI
+ ||align="left"| pAAV_RC_1.2 SDM SalI
+|-
+| align="left" | '''Date''' ||align="left"| 05.08.2010 ||align="left"| 05.08.2010
+|-
+| align="left" | '''given glycerol-stock no.''' ||align="left"| B126 ||align="left"| B127
+|-
+| align="left" | '''given plasmid no.''' ||align="left"| p158 ||align="left"| p159
+|}
+<br />
+TO do: Test digestion and sequencing!!!
-*587 BAP clone 2.3
+===81.Labortag 06.08.2010===
-*453 RGD clone 4.3
+====<p style="font-size:15px; background-color:#66bbff;"><b>Cloning Rep40 & Rep52 into pSB1C3</b></p>====
+Intention: get biobrick ready <br>
+Investigator: Patrick <br>
+PCR of pKEX-2XL.Rep 40 (P22) and pKEX-2XL.Rep 52 (P23) following gelrun (1%) and gelextraction. <br>
+Used Primers:
+* Praefix Rep40_52ex (O94)
+* Suffix Rep 40_68ex (O96)
+* Suffix Rep 52_78ex (O97)
+<br>
+PCR programm of Rep40:
+*98°C   1 min
+<br>
+*98°C   15 sec
+*63°C   25 sec
+*72°C   15 sec   Repeat this cycle 8 times.
+<br>
+*98°C   15 sec
+*68°C   25 sec
+*72°C   15 sec   Repeat this cycle 17 times.
+<br>
+*72°C   5 min
+*Hold 4°C
+<br>
+<br>
+PCR programm of Rep52:
+*98°C   1 min
+<br>
+*98°C   15 sec
+*62°C   25 sec
+*72°C   20 sec   Repeat this cycle 8 times.
+<br>
+*98°C   15 sec
+*66°C   25 sec
+*72°C   20 sec   Repeat this cycle 17 times.
+<br>
+*72°C   5 min
+*Hold 4°C
-The other samples didn't contain any inserts or had wrong insertions. Apparently, the vector tends to religate easily. A possible reason for the religation of the incompatible ends is the overnight ligation at 18°C. We sent preps of the remaining 7 ligations for sequencing and will prep new clones or repeat the ligation tomorrow, depending on the new sequences.
+<br>
+{| border="1"
+|'''ingredients'''|| align="right" |'''Rep 40'''|| align="right" |'''Rep40 + DMSO'''|| align="right" |'''Rep52'''|| align="right" |''' Rep52 + DMSO
+|-
+| 5x Phusion HF buffer||  align="right" |10 µl || align="right" |10 µl|| align="right" |10 µl|| align="right" |10 µl
+|-
+|10 mM dNTP mix||  align="right" |1 µl || align="right" |1 µl|| align="right" |1 µl|| align="right" |1 µl
+|-
+|for Primer O94 (1:10 dilution, 05 µM)||  align="right" |2,5 µl  || align="right" |2,5 µl|| align="right" |2,5 µl|| align="right" |2,5 µl
+|-
+|rev Primer (1:10 dilution, 0,5 µM) ||  align="right" |2,5 µl O96|| align="right" |2,5 µl O96|| align="right" |2,5 µl O97|| align="right" |2,5 µl O97
+|-
+|DNA template ||  align="right" | 1 µl, 112,7 ng/µl|| align="right" |1 µl, 112,7 ng/µl|| align="right" |0,9 µl, 142,3 ng/µl|| align="right" |0,9 µl, 142,3 ng/µl
+|-
+|DMSO||  align="right" |0 µl|| align="right" |0,5 µl|| align="right" |0 µl|| align="right" |0,5 µl
+|-
+|Phusion Polymerase||  align="right" |0,5 µl|| align="right" |0,5 µl|| align="right" |0,5 µl|| align="right" |0,5 µl
+|-
+|H2O||  align="right" |32,5 µl|| align="right" |32 µl|| align="right" |32,6 µl|| align="right" |32,1 µl
+|-
+|Total volume||  align="right" |50 µl|| align="right" |50 µl|| align="right" |50 µl|| align="right" |50 µl
+|}
+<br>
-<p style="font-size:13px; color:#66bbff;"><b>
+Ecpected size of Rep40: 940 bp, expected size of Rep52:1198 bp. There are two samples of Rep40 and Rep52 and the PCR of one of each was run with 1% DMSO because the Rep40 Praefix has a strong secondary structure and was used as a primer for Rep 40 and Rep 52<br>
-Comment:</b> Clones 1.4, 6.4, 9.4, 11.4, 12.4, 13.4, 14.4 were sent for sequencing.  For sequencing results go to labday 03.09.10. </p>.
+<br>
+[[File:IM000026_Patrick.JPG|400px]]
+<br>
+<br>
+Digestion of pSB1C3 (P51.1) with EcoRI-HF and SpeI following gelrun (0.8%) and gelextraction. <br>
+Expected size of the fragments: about 2000 bp and 800bp <br>
+<br>
+[[File:IM000028_Patrick.JPG‎|500px]]
+<br>
+<br>
-====<p style="font-size:15px; background-color:#66bbff;"><b>Mini-preps of pSB1C3_SV40 and pCerulean_VP1_NLS</b></p>====
+All marked fragments were extracted. The Gelextraction was performed according to the standard protocol following a digestion of the PCR products with EcoRI HF and SpeI and a purification of the PCR product. The Ligation was not performed according to the standard protocol: 1 µl T4 DNA Ligase, 1 µl (10x) Buffer, 3 µl vector pSB1C3 (60 ng/µl) and 5 µl insert (all concentrations about 100 ng/µl). The Transformation (with BL21) was performed according to the standard protocol. Tomorrow there will hopefully be some clones on the agar plates.
-<b>Investigator: Bea (Chris L) <br /></b>
+====<p style="font-size:15px; background-color:#66bbff;"><b>BioBrick Assembly of pSB1C3_beta globin_mVenus</b></p>====
+Investigator: <b>Bea </b>
 <br />
-Mini-Prep was performed according to the standard protocol
+<p style="font-size:13px; color:#003399;"><b>Comments</b>: BioBricks are ready to use. The sequenced pSB1C3_beta globin (P133) and pGA14_mVenus (P60) will be digested with different enzymes and will be assembled in order to produce the first step in assembling the whole vector together. </p>
 <br />
-<li>P363 = pSB1C3_SV40 clone 1 = 277,70 ng/µl
+<ul>
-<li>P364 = pSB1C3_SV40 clone 2 = 265,01 ng/µl
+<li>First the plasmids P133 and P60 were digested:</li>
-<li>P365 = pCerulean_VP1up_NLS (1) clone 1 = 473,14 ng/µl
+</ul>
-<li>P366 = pCerulean_VP1up_NLS (1) clone 2 = 455,88 ng/µl
+<table border=2 cellpadding=1 cellspacing=1 width=528 style='border-collapse:
-<li>P367 = pCerulean_VP1up_NLS (1) clone 3 = 482,86 ng/µl
+ collapse;table-layout:fixed;width:396pt'>
-<li>P368 = pCerulean_VP1up_NLS (2) clone 1 = 438,52 ng/µl
+ <tr height=20 style='height:15.0pt'>
-<li>P369 = pCerulean_VP1up_NLS (2) clone 2 = 478,00 ng/µl
+  <td height=20 class=xl65 width=176 style='height:15.0pt;width:132pt'>&nbsp;</td>
-<li>P370 = pCerulean_VP1up_NLS (2) clone 3 = 419,00 ng/µl
+  <td class=xl66 width=176 style='border-left:none;width:132pt'>pSB1C3_betaglobin/µL</td>
+  <td class=xl66 width=176 style='border-left:none;width:132pt'>pGA14_mVenus/µL</td>
+ </tr>
+ <tr height=20 style='height:15.0pt'>
+  <td height=20 class=xl67 width=176 style='height:15.0pt;border-top:none;
+  width:132pt'>DNA</td>
+  <td class=xl68 style='border-top:none;border-left:none'>7</td>
+  <td class=xl68 style='border-top:none;border-left:none'>9</td>
+ </tr>
+ <tr height=20 style='height:15.0pt'>
+  <td height=20 class=xl67 width=176 style='height:15.0pt;border-top:none;
+  width:132pt'>BSA (100x)</td>
+  <td class=xl68 style='border-top:none;border-left:none'>0,2</td>
+  <td class=xl68 style='border-top:none;border-left:none'>0,2</td>
+ </tr>
+ <tr height=40 style='height:30.0pt'>
+  <td height=40 class=xl67 width=176 style='height:30.0pt;border-top:none;
+  width:132pt'>Buffer 4<span style='mso-spacerun:yes'>   </span>(10x)</td>
+  <td class=xl68 style='border-top:none;border-left:none'>2</td>
+  <td class=xl68 style='border-top:none;border-left:none'>2</td>
+ </tr>
+ <tr height=40 style='height:30.0pt'>
+  <td height=40 class=xl67 width=176 style='height:30.0pt;border-top:none;
+  width:132pt'>Enzyme XbaI<span style='mso-spacerun:yes'> </span></td>
+  <td class=xl68 style='border-top:none;border-left:none'>1</td>
+  <td class=xl68 style='border-top:none;border-left:none'>1</td>
+ </tr>
+ <tr height=40 style='height:30.0pt'>
+  <td height=40 class=xl67 width=176 style='height:30.0pt;border-top:none;
+  width:132pt'>Enzyme AgeI</td>
+  <td class=xl68 style='border-top:none;border-left:none'>1</td>
+  <td class=xl68 style='border-top:none;border-left:none'>1</td>
+ </tr>
+ <tr height=20 style='height:15.0pt'>
+  <td height=20 class=xl67 width=176 style='height:15.0pt;border-top:none;
+  width:132pt'>H2O</td>
+  <td class=xl68 style='border-top:none;border-left:none'>8,8</td>
+  <td class=xl68 style='border-top:none;border-left:none'>6,8</td>
+ </tr>
+ <tr height=40 style='height:30.0pt'>
+  <td height=40 class=xl67 width=176 style='height:30.0pt;border-top:none;
+  width:132pt'>Total volume</td>
+  <td class=xl69 style='border-top:none;border-left:none'>20</td>
+  <td class=xl69 style='border-top:none;border-left:none'>20</td>
+ </tr>
+ <tr height=0 style='display:none'>
+  <td width=176 style='width:132pt'></td>
+  <td width=176 style='width:132pt'></td>
+  <td width=176 style='width:132pt'></td>
+ </tr>
+</table>
+<ul>
+<li> Incubation of plasmids at 37°C for 2 hours </li>
+<li> Load samples on preparative 1% agarose gel and run at 110 V, 45 minutes </li>
+</ul>
+<br/>
+<b>Results:</b> As it can be seen in the picture below, digestion of the vector pSB1C3_betaglobin (left lane) revealed a band at around 2500 - 3000 bp. The expected size after digetsing with SpeI and PstI was: 2555 bp. The band ran a little bit higher than expected, anyhow the band was cut out of the gel. The right lane belongs to the pGA14_mVenus which was digested with XbaI and PstI which resulted in two fragments. mVENUS was digested. Expected sizes were: mVenus = 756bp and pGA14 = 2900bp. The expected sizes correspond to the bands seen in the picture below. The smaller fragment belonging to mVenus was cut out of the gel as well.
 <br />
-Construct were digested with XbaI and PstI for 45 minutes at 37°C. The loading plan on the 1% agarose gel looks like this:
 <br />
+[[File:Freiburg10 pSB1C3 betaglobin mVenus 06 08 2010.jpg|550px]]
 <br />
-_M_  ___ _363_  ___  _364_  _365_  _366_  _367_  _368_  _369_  _370_  ___
 <br />
+After gel extraction has been performed, the concentrations of the two fragments were measured and we obtained following concentrations:
+<ul>
+<li>c(pSB1C3_betaglobin) = 15,62 ng/µL </li>
+<li>c(mVenus) = 6,83  ng/µL </li>
+</ul>
+<br />
+For ligation the T4-Ligase were used.
+<ul>
+<li>v(pSB1C3_betaglobin) = 2,64 µL </li>
+<li>v(mVenus) =5,36 µL </li>
+<li>v(10xT4 Ligase buffer) = 1 µL </li>
+<li>v(T4-Ligase) = 1 µL </li>
+<li><b>Total volume = 10 µL </b></li>
+</ul>
+<br />
+Additionally a control ligation was performed.
+<ul>
+<li>v(pSB1C3_betaglobin) = 2,64 µL </li>
+<li>v(H<sub>2</sub>0) =5,36 µL </li>
+<li>v(10xT4 Ligase buffer) = 1 µL </li>
+<li>v(T4-Ligase) = 1 µL </li>
+<li><b>Total volume = 10 µL </b></li>
+<li>Ligation duration was 45 minutes on room temperature.</li>
+</ul>
+<br />
+After ligation a transformation was performed.
+<ul>
+<li> Used bacterial strain: XL1-B</li>
+<li> LB-agar plates containing chloramphenicol were plated and put in the 37°C room over night</li>
+</ul>
 <br />
-<b>Results:</b>
+<p style="font-size:13px; color:#003399;"><b>To do</b>: Mini-Prep and test digestion in order to verify assembly of beta globin and YFP. After verification of the fusion of the two fragments this construct is ready for the next BioBrick assembly step. </p>
-P365 was sent for sequencing because test digestion looks goos. In contrast to the SV40 appraoch. This needs to be repeated tomorrow.<br />
+====<p style="font-size:15px; background-color:#ff00ff;">'''Test digestion of SalI SDM'''</p>====
+Investigator: <b>Hanna</b>
+<br/>
+<p style="font-size:15px; font-weight: bold; color:#ff00ff;">Test digestion</p>
+<ul>
+<li>buffer used: 3 ; Restriction-enzymes used: Enzyme 1 (no. Lab: 53): SalI ; Enzyme 2: XbaI </li>
+<li>Plasmid
 <ul>
-<li>Plasmid: pCerulean_VP1up_NLS</li>
+<li>Given Plasmid-Number: P158; DNA concentration: 398.8 ng/µL ;</li>
-<li>Plasmid number: P365</li>
+<li>Given Plasmid-Number: P159; DNA concentration: 437.4 ng/µL ;</li>
-<li>Tube name: SB1</li>
-<li>Primer used: CMV-F</li>
 </ul>
+</ul>
+<br />
+<br />
+{| border="1"
+| align="left" | '''Components''' ||align="left"| '''P158 Volume/µL''' ||align="left"| '''P159 Volume/µL'''
+|-
+| align="left" | DNA ||align="left"| 2.5 ||align="left"| 2.3
+|-
+| align="left" | BSA (10x) ||align="left"| 1 ||align="left"| 1
+|-
+| align="left" | Buffer 3 (10x) ||align="left"| 1 ||align="left"| 1
+|-
+| align="left" | SalI (no. Lab: 53) ||align="left"| 0.5 ||align="left"| 0.5
+|-
+| align="left" | XbaI ||align="left"| 0.75 ||align="left"| 0.75
+|-
+| align="left" | H<sub>2</sub>O ||align="left"| 4.25 ||align="left"| 4.45
+|-
+| align="left" | <b>Total volume</b> ||align="left"| <b>10</b> ||align="left"| <b>10</b>
+|}
+<br />
+Incubation: 1 h
+<br />
+<p style="font-size:15px; font-weight: bold; color:#ff00ff;">Agarose-Gel:</p>
+<br />
+.5  g Agarose, 50 mL TBE (1 %),3 µL GELRED, at 115 Volt, running time: 45 minutes
+<br />
+<br />
+{| border="1" cellspacing="0" cellpadding="2" bordercolor="black"
+!Sample
+!Sample/µl]
+!Loading dye (5x)/µl
+!Expected size 1 (if SDM didn't work)
+!Expected size 2 (if SDM didn't work)
+!Expected size 3 (if SDM didn't work)
+|--
+|P158
+|10 µl
+|2 µl
+|6129 bp
+|1143 bp
+|61 bp
+|--
+|P159
+|10 µl
+|2 µl
+|6129 bp
+|1143 bp
+|61 bp
+|--
+|}
+{| align=right
+|}
+<br />
+*Marker: GeneRuler ladder mix
+{| border="1"
+|
+!Marker /µL
+!Sample P158 /µl
+!Sample P159 /µl
+!Marker /µL
+|-
+!Lane
+|6.5
+|10
+|10
+|7
+|-
+|}
+<br />
+[[File:Freiburg10 Test digestion SalI1.jpg|600px]] <br/>
-====<p style="font-size:15px; background-color:#ff00ff;"><b>Mini-Prep and test digestion of pCerulean_Zegfr:1907 and pCerulean_6xHis_MiddleLinker</b></p>====
+<b>Comments:</b> Test digestion looked good: No 1143 bp fragment was detectable in neither test digestion. <br/>
-<b>Investigator: Hanna <br /></b>
+P158 was sent for sequencing to GATC. <br/>
+====<p style="font-size:15px; background-color:#ff00ff;">'''ITR test digestion of pAAV_MCS'''</p>====
+Investigator: <b>Hanna</b>
 <br/>
-<p style="color:#ff00ff;"><b>Comment:</b> Zegfr:1907 (Affibody) and the His-Tag which was coupled to the middle linker were cloned into pCerulean. 3 clones of each construct were picked yesterday. </p>
+<p style="color:#ff00ff;"><b>Comment:</b> Because sequencing of the right ITR delivered that perhaps a 15 bp fragment is missing in the sequence, we wanted to check, whether this fragment is also not present in the original pAAV_MCS plasmid or whether the loss of these 15 bp happened during cloning. </p>
 <br/>
+<p style="font-size:15px; font-weight: bold; color:#ff00ff;">Test digestion</p>
+<ul>
+<li>buffer used: 4 ; Restriction-enzymes used: Enzyme 1: NotI; Enzyme 2: PstI</li>
+<li>Plasmid
+<ul>
+<li>Plasmid-Number: from Sven; DNA concentration: 259 ng/µL ;</li>
+</ul>
+</ul>
+<br />
+<br />
+{| border="1"
+| align="left" | '''Components''' ||align="left"| '''Volume/µL'''
+|-
+| align="left" | DNA ||align="left"| 3.8
+|-
+| align="left" | BSA (10x) ||align="left"| 1.5
+|-
+| align="left" | Buffer 4 (10x) ||align="left"| 1.5
+|-
+| align="left" | NotI-HF ||align="left"| 0.75
+|-
+| align="left" | PstI-HF ||align="left"| 0.75
+|-
+| align="left" | H<sub>2</sub>O ||align="left"| 3.2
+|-
+| align="left" | <b>Total volume</b> ||align="left"| <b>15</b>
+|}
+<br />
+Incubation: 1 h
+<br />
+<p style="font-size:15px; font-weight: bold; color:#ff00ff;">Agarose-Gel:</p>
+<br />
+.5  g Agarose, 50 mL TBE (1 %),3 µL GELRED, at 115 Volt, running time: 45 minutes
+<br />
+<br />
+{| border="1" cellspacing="0" cellpadding="2" bordercolor="black"
+!Sample
+!Sample/µl]
+!Loading dye (5x)/µl
+!Expected size <b>ITRs</b>
+!Expected size 2
+!Expected size 3
+!Expected size 4
+|--
+|pAAV_MCS
+|15 µl
+|2 µl
+|145 bp
+|1216 bp
+|555 bp
+|2608 bp
+|--
+|}
+{| align=right
+|}
+<br />
+*Marker: GeneRuler ladder mix
+{| border="1"
+|
+!Marker /µL
+!Sample /µl
+!Marker /µL
+|-
+!Lane
+|6.5
+|12
+|6.5
+|-
+|}
+<br />
+[[File:Freiburg10 testDigestion pAAV MCS.jpg|700px]] <br/>
+<p style="font-size:15px; color:#ff00ff;"><b>Comments:</b> The test digestion showed that there're two bands between the 100 and 200 bp marker nucleotides! By comparing the gel picture with the last mini-prep digestion of the fancy method we found out that the space between the two bands are similar. Because of that we assumed that the 15 pb are already missing in the original Stratagene plasmid!!!  </p> <br/>
+<p style="font-size:15px; color:#800080;"><b>Conclusion:</b> Because we already tested the Stratagene Kit via YFP expression, we can conclude that the usage of the "wrong" rigth ITR works. Therefore we decided to continue working with this "mutated" = <b> ENGINEERED </b> :) right ITR as BioBrick.</p> <br/>
+====<p style="font-size:15px; background-color:#66bbff;"><b>Miniprep of pSBC13_Rep78, pSB1C3_Rep68, pSB1C3_AAP, pSB1C3_rightITR and psB1C3_leftITR</b></p>====
+<p style="font-size:13px; color: blue;">Plasmid Mini-Prep</p>
+Investigator: Kerstin<br>
+<br>
-<p style="font-size:15px; font-weight: bold; color: #ff00ff;">Plasmid Mini-Prep</p>
-*new vector name: pCerulean_Zegfr:1907 and pCerulean_6xHis_MiddleLinker
 <br />
-<b><u>Glycerol Stocks</u></b> <br/>
+<u><b>Glycerol Stocks</b></u> <br>
-<b>1. pCerulean_Zegfr:1907</b>
+<b>pSB1C3_Rep78</b>
 {| border="1"
-| align="left" |  ||align="left"| '''Clone 1''' ||align="left"| '''Clone 2''' ||align="left"| '''Clone 3'''
+| align="left" |  ||align="left"| '''Clone 1''' ||align="left"| '''Clone 2'''
 |-
-| align="left" | '''Bacteria strain''' ||align="left"| XL1b ||align="left"| XL1b  ||align="left"| XL1b
+| align="left" | '''Bacteria strain''' ||align="left"| BL-21 ||align="left"| BL-21
 |-
-| align="left" | '''Plasmidname''' ||align="left"| pCerulean_Zegfr:1907 ||align="left"| pCerulean_Zegfr:1907 ||align="left"| pCerulean_Zegfr:1907
+| align="left" | '''given glycerol-stock no.''' ||align="left"| B128 ||align="left"| B129
 |-
-| align="left" | '''Date''' ||align="left"| 2.9.10 ||align="left"| 2.9.10 ||align="left"| 2.9.10
+| align="left" | '''given plasmid no.''' ||align="left"| P160 ||align="left"| p161
 |-
-| align="left" | '''given glycerol-stock no.''' ||align="left"| B275 ||align="left"| B276 ||align="left"| B277
+| align="left" | '''DNA-concentration ng/µl''' ||align="left"| 139,1 ||align="left"| 71,0
+|}
+<b>pSB1C3_2_Rep78</b>
+{| border="1"
+| align="left" |  ||align="left"| '''Clone 1''' ||align="left"| '''Clone 2'''
 |-
-| align="left" | '''given plasmid no.''' ||align="left"| P371 ||align="left"| P372 ||align="left"| P373
+| align="left" | '''Bacteria strain''' ||align="left"| BL-21 ||align="left"| BL-21
+|-
+| align="left" | '''given glycerol-stock no.''' ||align="left"| B130 ||align="left"| B131
+|-
+| align="left" | '''given plasmid no.''' ||align="left"| P162 ||align="left"| p163
+|-
+| align="left" | '''DNA-concentration ng/µl''' ||align="left"| 112,1 ||align="left"| 79,7
 |}
+<b>pSB1C3_Rep68</b>
+{| border="1"
+| align="left" |  ||align="left"| '''Clone 1''' ||align="left"| '''Clone 2'''
+|-
+| align="left" | '''Bacteria strain''' ||align="left"| BL-21 ||align="left"| BL-21
+|-
+| align="left" | '''given glycerol-stock no.''' ||align="left"| B132 ||align="left"| B133
+|-
+| align="left" | '''given plasmid no.''' ||align="left"| P164 ||align="left"| p165
+|-
+| align="left" | '''DNA-concentration ng/µl''' ||align="left"| 80,2 ||align="left"| 72,8
+|}
+<b>pSB1C3_2_Rep68</b>
+{| border="1"
+| align="left" |  ||align="left"| '''Clone 1''' ||align="left"| '''Clone 2'''
+|-
+| align="left" | '''Bacteria strain''' ||align="left"| BL-21 ||align="left"| BL-21
+|-
+| align="left" | '''given glycerol-stock no.''' ||align="left"| B134 ||align="left"| B135
+|-
+| align="left" | '''given plasmid no.''' ||align="left"| P166 ||align="left"| p167
+|-
+| align="left" | '''DNA-concentration ng/µl''' ||align="left"| 85,6 ||align="left"| 69,1
+|}
+<b>pSB1C3_AAP</b>
+{| border="1"
+| align="left" |  ||align="left"| '''Clone 1''' ||align="left"| '''Clone 2'''
+|-
+| align="left" | '''Bacteria strain''' ||align="left"| BL-21 ||align="left"| BL-21
+|-
+| align="left" | '''given glycerol-stock no.''' ||align="left"| B136 ||align="left"| B137
+|-
+| align="left" | '''given plasmid no.''' ||align="left"| P168 ||align="left"| p169
+|-
+| align="left" | '''DNA-concentration ng/µl''' ||align="left"| 63,6 ||align="left"| 56,3
+|}
+<b>pSB1C3_2_AAP</b>
+{| border="1"
+| align="left" |  ||align="left"| '''Clone 1''' ||align="left"| '''Clone 2'''
+|-
+| align="left" | '''Bacteria strain''' ||align="left"| BL-21 ||align="left"| BL-21
+|-
+| align="left" | '''given glycerol-stock no.''' ||align="left"| B138 ||align="left"| B139
+|-
+| align="left" | '''given plasmid no.''' ||align="left"| P170 ||align="left"| p171
+|-
+| align="left" | '''DNA-concentration ng/µl''' ||align="left"| 135,1 ||align="left"| 114,2
+|}
+<b>pSB1C3_rightITR</b>
+{| border="1"
+| align="left" |  ||align="left"| '''Clone 1''' ||align="left"| '''Clone 2'''
+|-
+| align="left" | '''Bacteria strain''' ||align="left"| BL-21 ||align="left"| BL-21
+|-
+| align="left" | '''given glycerol-stock no.''' ||align="left"| B140 ||align="left"| B141
+|-
+| align="left" | '''given plasmid no.''' ||align="left"| P172 ||align="left"| p173
+|-
+| align="left" | '''DNA-concentration ng/µl''' ||align="left"| 73,7 ||align="left"| 66,4
+|}
+<b>pSB1C3_leftITR</b>
+{| border="1"
+| align="left" |  ||align="left"| '''Clone 1''' ||align="left"| '''Clone 2'''
+|-
+| align="left" | '''Bacteria strain''' ||align="left"| BL-21 ||align="left"| BL-21
+|-
+| align="left" | '''given glycerol-stock no.''' ||align="left"| B142 ||align="left"| B143
+|-
+| align="left" | '''given plasmid no.''' ||align="left"| P174 ||align="left"| p175
+|-
+| align="left" | '''DNA-concentration ng/µl''' ||align="left"| 74,9 ||align="left"| 80,3
+|}
+<br>
+'''Test digestion:'''<br>
+pSB1C3_Rep78, pSB1C3_Rep68 and pSB1C3_AAP were digested with XbaI and SpeI<br>
+pSB1C3_rightITR and pSB1C3_leftITR were digested with EcoRI and PstI.<br>
+<br>
+{| border="1"
+| components   || align="right" |volume of '''P160'''/µl ||volume of '''P161'''/µl||volume of '''P162/'''µl ||volume of '''P163'''/µl ||volume of '''P164'''/µl||volume of '''P165'''/µl||volume of '''P166'''µl ||volume of '''P167'''/µl||volume of '''P168'''µl ||volume of '''P169'''/µl||volume of '''P170'''/µl||volume of '''P171'''/µl||volume of '''P172'''/µl||volume of '''P173'''µl ||volume of '''P174'''/µl ||volume of '''P175'''/µl
+|-
+| DNA  ||5,8 ||11,3 ||7,1 ||10 ||9,9 ||10,9 ||9,3 ||11,6 ||12,5 ||14,2 ||5,9 ||7,0 ||10,9 ||12,0 ||10,7 ||9,7
+|-
+| BSA (10x) ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2
+|-
+| Buffer 4 (10x)||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2 ||2
+|-
+|Enzyme 1 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5
+|-
+|Enzyme 2 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5 ||0,5
+|-
+|H2O ||9,2 ||3,7 ||7,9 ||5,0 ||5,1 ||4,1 ||5,7 ||3,4 ||2,5 ||0,8 ||9,1 ||8 ||4,1 ||3 ||4,3 ||5,3
+|-
+|'''Total volume /µl'''||20 ||20 ||20 ||20 ||20 ||20 ||20 ||20 ||20 ||20 ||20 ||20 ||20 ||20 ||20 ||20
+|}
+<br />
+'''Expected sizes:'''<br>
+*Rep78: 1,8 kb
+*Rep68: 1,6kb<br>
+*AAP: 650bp <br>
+*left ITR: 150bp
+*right ITR: 150bp
+<br>
+<p style="font-size:13px; color:#11bb88;">'''Results of samples loaded 1,5% agarose gel and ran ~50 minutes at 115 V:''' </p>
+[[File:Freiburg10 test digestion itr und aap.jpg|400px]]
+<br>
+<p style="font-size:13px; color:#11bb88;">'''Results of samples loaded 0,8% agarose gel and ran ~50 minutes at 115 V:''' </p>
+[[File:Freiburg10 test digestion rep 78 u. 68.jpg|400px]]
+<p style="font-size:13px; color:#11bb56;">'''Sequencing''' </p>
+P160, P165 and P170 were send for sequencing.
+===82.Labortag 07.08.2010===
+====<p style="font-size:15px; background-color:#66bbff;"><b>Cellculture</b></p>====
+HEK 293 cells were split and seeded according to the standard protocol: 2x T75 flask and 10x10cm cellculture dishes. Investigator: Patrick
+====<p style="font-size:15px; background-color:#66bbff;"><b>Continuation: Cloning Rep40 & Rep52 into pSB1C3</b></p>====
+Investigator: Patrick <br>
+Results: no clones could be picked because there were no clones. Maybe the PCR purification or one of the following steps did not work (the PCR purifications were quite bad) so i purified the PCR products again yielding very low DNA concentrations (0-13,28 ng/µl) and still very obvious pollution of the sample. Nonetheless a ligation with the insert Rep40+DMSO, Rep52, Rep52+DMSO and the vector pSB1C3 was carried out following a transformation and according to the standard protocols. Hopefully there will be some clones tomorrow.
+====<p style="font-size:15px; background-color:#66bbff;"><b>Mini-Prep and test digestion of pSB1C3_SDM_SspI/PvuII</b></p>====
+'''Investigator: Jessica'''<br>
+<br>
+<p style="font-size:18px; font-weight: bold; color:#66bbff;"><u>Plasmid Mini-Prep</u></p>
+*new vector name: pSB1C3_SDM_SspI/PvuII
 <br />
-<b>2. pCerulean_6xHis_MiddleLinker</b>
+<u><b>Glycerol Stocks</b></u> <br>
+<b>pSB1C3_SDM_SspI/PvuII</b>
 {| border="1"
 | align="left" |  ||align="left"| '''Clone 1''' ||align="left"| '''Clone 2''' ||align="left"| '''Clone 3'''
 |-
-| align="left" | '''Bacteria strain''' ||align="left"| XL1b ||align="left"| XL1b  ||align="left"| XL1b
+| align="left" | '''Bacteria strain''' ||align="left"| BL21 ||align="left"| BL21  ||align="left"| BL21
 |-
-| align="left" | '''Plasmidname''' ||align="left"| pCerulean_6xHis_MiddleLinker ||align="left"| pCerulean_6xHis_MiddleLinker ||align="left"| pCerulean_6xHis_MiddleLinker
+| align="left" | '''Plasmidname''' ||align="left"| pSb1C3_SDM_SspI/PvuII ||align="left"| pSb1C3_SDM_SspI/PvuII ||align="left"| pSb1C3_SDM_SspI/PvuII
 |-
-| align="left" | '''Date''' ||align="left"| 2.9.10 ||align="left"| 2.9.10 ||align="left"| 2.9.10
+| align="left" | '''Date''' ||align="left"| 7.8.10 ||align="left"| 7.8.10 ||align="left"| 7.8.10
 |-
-| align="left" | '''given glycerol-stock no.''' ||align="left"| B278 ||align="left"| B279 ||align="left"| B280
+| align="left" | '''given glycerol-stock no.''' ||align="left"| B144 ||align="left"| B145 ||align="left"| B146
 |-
-| align="left" | '''given plasmid no.''' ||align="left"| P374 ||align="left"| P375 ||align="left"| P376
+| align="left" | '''given plasmid no.''' ||align="left"| P157.1 ||align="left"| P157.2 ||align="left"| P157.3
 |}
+<br>
+<p style="font-size:15px; font-weight: bold; color:#66bbff;">Test digestion</p>
+*buffer used: 2 ; Restriction-enzymes used: Enzyme 1 SspI ; Enzyme 2 PvuII
+*Plasmid: pSB1C3_SDM_SspI/PvuII:
+**Given Plasmid-Number: P157.1; DNA concentration: 246,3 ng/µL ;
+**Given Plasmid-Number: P157.2; DNA concentration: 231,7 ng/µL ;
+**Given Plasmid-Number: P157.3; DNA concentration: 219,6 ng/µL ;
 <br />
-<p style="font-size:15px; font-weight: bold; color: #ff00ff;">Test digestion</p>
-*buffer used: 4; Restriction-enzymes used: Enzyme 1 PstI-HF ; Enzyme 2 EcoRI-HF
-*Plasmid
-**Given Plasmid-Number: 371; DNA concentration: 381.3 ng/µL;
-**Given Plasmid-Number: 372; DNA concentration: 377.5 ng/µL;
-**Given Plasmid-Number: 373; DNA concentration: 409.7 ng/µL;
-**Given Plasmid-Number: 374; DNA concentration: 404.2 ng/µL;
-**Given Plasmid-Number: 375; DNA concentration: 366.1 ng/µL;
-**Given Plasmid-Number: 376; DNA concentration: 375.0 ng/µL;
-<br />
-'''Comments:''':)
-<br />
-<br />
-<b>Pipetting scheme for each test digestion:</b>
 {| border="1"
-| align="left" | <b>Components</b> ||align="left"| <b>Volume/µL</b>
+| align="left" | '''Components''' ||align="left"| <b>P157.1</b> Volume/µL ||align="left"| <b>P157.2</b> Volume/µL ||align="left"| <b>P157.3</b> Volume/µL
 |-
-| align="left" | DNA ||align="left"| 2.7
+| align="left" | DNA ||align="left"| 2,8 ||align="left"| 3,0 ||align="left"| 3,19
 |-
-| align="left" | BSA (10x) ||align="left"| 1
+| align="left" | BSA (10x) ||align="left"| - ||align="left"| - ||align="left"| -
 |-
-| align="left" | Buffer no. 4 (10x) ||align="left"| 1
+| align="left" | Buffer no. 2 (10x) ||align="left"| 1 ||align="left"| 1 ||align="left"| 1
 |-
-| align="left" | EcoRI-HF ||align="left"| 0.5
+| align="left" | Enzyme 1 SspI ||align="left"| 0.5 ||align="left"| 0.5 ||align="left"| 0.5
 |-
-| align="left" | PstI-HF ||align="left"| 0.5
+| align="left" | Enzyme 2 PvuII ||align="left"| 0.5 ||align="left"| 0.5 ||align="left"| 0.5
 |-
-| align="left" | H<sub>2</sub>O ||align="left"| 4.3
+| align="left" | H<sub>2</sub>O ||align="left"| 5,2 ||align="left"| 5 ||align="left"| 4,81
 |-
-| align="left" | <b>Total volume</b> ||align="left"| <b>10</b>
+| align="left" | '''Total volume''' ||align="left"| <b>10</b>  ||align="left"| <b>10</b> ||align="left"| <b>10</b>
 |}
 <br />
-*Incubation: 55 minutes
+*Incubation: 45 min
 <br />
-<p style="font-size:15px; font-weight: bold; color: #ff00ff;">Agarose-Gel:</p>
+<p style="font-size:15px; font-weight: bold; color:#66bbff;">Agarose-Gel:</p>
 <br />
-.875 g Agarose, 50 mL TAE (1.75 %), 3 µL EthBr, at 115 Volt, running time: 35 minutes
+.45 g Agarose, 50 mL <b>TAE</b>, 3 µL GELRED, at 115 Volt, running time: 45 minutes
 <br />
 <br />
@@ Line 433: / Line 2,159: @@
 !Sample/µl]
 !Loading dye (6x)/µl
-!Expected size
 |--
-|pCerulean_Zegfr:1907 clone 1
+|P157.1
 |10 µl
-|2 µl
+|1,6 µl
-|231 bp
 |--
-|pCerulean_Zegfr:1907 clone 2
+|P157.2
 |10 µl
-|2 µl
+|1,6 µl
-|231 bp
 |--
-|pCerulean_Zegfr:1907 clone 3
+|P157.3
 |10 µl
-|2 µl
+|1,6 µl
-|231 bp
-|--
-|pCerulean_6xHis_MiddleLinker clone 1
-|10 µl
-|2 µl
-|105 bp
-|--
-|pCerulean_6xHis_MiddleLinker clone 2
-|10 µl
-|2 µl
-|105 bp
-|--
-|pCerulean_6xHis_MiddleLinker clone 3
-|10 µl
-|2 µl
-|105 bp
 |--
@@ Line 474: / Line 2,185: @@
 |
 !Marker /µL
-!Sample P371 /µl
+!Sample P157.1 /µL
-!Sample P372 /µl
+!Sample P157.2 /µL
-!Sample P373 /µl
+!Sample P157.3 /µL
-!Sample P374 /µl
-!Sample P375 /µl
-!Sample P376 /µl
 |-
 !Lane
-|5
+|7
-|12
+|10
-|12
+|10
-|12
+|10
-|12
-|12
-|12
 |-
 |}
 <br />
-'''Comments:''' Test digestion looked well: <br/>
+<br>
+I expect one cut from the PvuII RS in the CFP --> linearized <br>
+[[File:Prep pSB1C3_SDM_SspIPvuII.jpg|400px]] <br>
+<br>
+<b>Comment:</b><br>
+<br>
+<p style="font-size:13px; color:#ff0000;">'''''Comments:'''''Oh f... it makes no sense... if the cloning didn't work, there can just be 3 bands (one time SspI and twice PvuII). The results of the test digestion from aug 1th showed that there can be one RS PvuII more. but then you have a maximum of 4 bands. '''P157.2''' show '''5''' bands. i can't interpret this result at the moment. interpretation will follow</p> <br>
 <br/>
-[[File:Freiburg10 pCerulean Zegfr1907andpCerulean 6xHis ML.png|700px]]
-<br/>
-Clone 1 of each construct were sent for sequencing (P371 and P374 = HW1 and HW2). Used primer: GATC_std_CMV-F.
 <br/>
-====<p style="font-size:15px; background-color:#66bbff;"> Midi-Prep of pSB1C3_lITR_CMV_mVenus_hGH_rITR clone1 & pSB1C3_lITR_CMV_beta-globin_mVenus_rITR clone1</p>====
+====<p style="font-size:15px; background-color:#66bbff;"><b>Evaluation of test transformation with XL1 blue cells and pUCI</b></p>====
+'''Investigator: Kira'''<br>
-'''Investigators: Chris W. <br>
+Transformation was performed with lab XL1B and iGEM XL1B cells. iGEM plate contained just 25 colonies, while lab plate contained around 50 colonies.
-<p style="font-size:13px; color:#003399;"> Midi-Preps of pSB1C3_lITR_CMV_mVenus_hGH_rITR clone1=P377 and pSB1C3_lITR_CMV_beta-globin_mVenus_rITR clone1=P378</p>
+Conclusion: the production of competent cells has to be repeated.
-The Midi-Preps were performed according to the standard protocol yielding the following concentrations:
+====<p style="font-size:15px; background-color:#66bbff;"><b>Biobrick production of p5 promoter from pTAV2 and pAAV_RC</b></p>====
+'''Investigator: Kira'''<br>
+*'''PCR:
+DNA samples were diluted 1:100
+<br>
 {| border="1"
-| plasmid-no. || align="right" |P377|| align="right" |P378
+| '''Ingredients''' || align="right" |'''p 32''' ||align="right"|p 50
 |-
-| concentration (ng/µl)|| align="right" |325,04 || align="right" |561,15
+| 5X Phusion HF buffer ||  align="right" |10 µl||align="right"|10 µl
 |-
+| 10 mM dNTP mix||  align="right" |1µl ||align="right"|1 µl
+|-
+| forward primer: O114 ||  align="right" |2,5µl||align="right"|2,5 µl
+|-
+| reverse primer: O115 ||  align="right" |2,5 µl||align="right"|2,5 µl
+|-
+| DNA Template||  align="right" |0,3 µl||align="right"| 0,4 µl
+|-
+| DMSO ||  align="right" |0 µl||align="right"|0 µl
+|-
+| Phusion Polymerase||  align="right" |0,5 µl||align="right"| 0,5 µl
+|-
+|H<sub>2</sub>O||  align="right" |33,2 µl||align="right"|28,6 µl
+|-
+|Total volume||  align="right" |50 µl||align="right"| 50 µl
 |}
 <br>
-====<p style="font-size:15px; background-color:#66bbff;"><b>Mini-Prep and test digestion of the CD biobricks</b></p>====
-<b>Investigator: Kira <br /></b>
-[[File:mistake.png|thumb|right|200px]]
+PCR program:
-[[File:Cartoons48.jpg|thumb|right|200px|Ohne Worte *lach*]]
-Wh did you digest with eco and ndeI?? is there a spechía reasonn for it?? if the coonstruct was in the rfc standard  could digest it with the igem standard enzymes??
 {| border="1"
-| components   || align="right" |sample /µl
+|Cycles||Temperature||Time
 |-
-| DNA  ||  align="right" | 2,5
+|||98°C||1
 |-
-| BSA (100x) ||  align="right" | 0
+|8x||98°C||30"
 |-
-| Buffer ___4_ (10x)||  align="right" | 1,5
+|||60°C||25"
 |-
-|Enzyme NdeI (no.Lab:___)||  align="right" | 0,5
+|||72°C||6"
 |-
-|Enzyme EcoRI (no.Lab:___)||  align="right" |0,5
+|17x||98°C||30"
 |-
-|H<sub>2</sub>O||  align="right" |10
+|||70°C||25"
 |-
-|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | |15
+|||72°C||6"
+|-
+|1x||72°C||5'
+|-
+|Hold 4°C
 |}
+<br>
-<li> Incubation: 1 h
+Digestion of plasmid backbone:
+c (pSB1C3) = 151, 1 ng/ µl
+{| border="1"
+| align="left" | '''Components''' ||align="left"| <b>vector</b> Volume/µL
+|-
+| align="left" | DNA 1 µg  ||align="left"| 6,0 µl
+|-
+| align="left" | BSA (100x) ||align="left"| 0,2 µl
+|-
+| align="left" | Buffer no. 4 (10x) ||align="left"| 2,0 µl
+|-
+| align="left" | Enzyme 1 XbaI ||align="left"| 1 µl
+|-
+| align="left" | Enzyme 2 PstI HF ||align="left"| 1 µl
+|-
+| align="left" | H<sub>2</sub>O ||align="left"| 9,8 µl
+|-
+| align="left" | '''Total volume''' ||align="left"| <b>20</b>
+|}
 <br />
+incubation @ 37 C for approx. 2 h
+% agarose gel with PCR products:
+[[File:Freiburg10 PCR.jpg|400px]]
 <br />
-[[File:Freiburg10 test digestion of CD.jpg|500px|]]
+Concentrations after gel extraction:
+c(p32) = 67,95 ng/µl <br />
+c(p50) = 32,45 ng/µl <br />
+c(vector) = 7,54 ng/µl <br />
 <br />
+Digestion of PCR products:
+{| border="1"
+| align="left" | '''Components''' ||align="left"| <b>PCR product</b> Volume/µL
+|-
+| align="left" | DNA 1 µg  ||align="left"| 23,0 µl
+|-
+| align="left" | BSA (100x) ||align="left"| 0,3 µl
+|-
+| align="left" | Buffer no. 4 (10x) ||align="left"| 3,0 µl
+|-
+| align="left" | Enzyme 1 XbaI ||align="left"| 1,5 µl
+|-
+| align="left" | Enzyme 2 PstI HF ||align="left"| 1,5 µl
+|-
+| align="left" | H<sub>2</sub>O ||align="left"| 0,7 µl
+|-
+| align="left" | '''Total volume''' ||align="left"| <b>30</b>
+|}
 <br />
-Sample 1 was sent for sequencing
+Concentrations after PCR purification:
-<br/>
-===109. labday 03.09.2010===
+c(p32) = 21, 63 ng/µl <br />
-====<p style="font-size:15px; background-color:#ff00ff;"><b>Miniprep and test digestion of pSB1C3_lITR_pTERT_ßglobin_mVenus_hGH_rITR</b></p>====
+c(p50) = 19,48 ng/µl <br />
-<b>Investigator: Achim <br /></b>
+<br />
-<br/>
-Comment: The test digestion did not show the expected fragments of 2000 and 2500 bp. the photo was exposed too long to see distinct bands. Digestion will be repeated.
-[[File:AA1.png|100px]]
+Ligation:
-<br/>
-====<p style="font-size:15px; background-color:#ff00ff;"><b>Sequencing results</b></p>====
+Quickligase was used for ligation.
-<b>Investigator: Hanna <br /></b>
-<br/>
+p32 DNA-Mix: 8 µl vector + 1 µl insert <br />
-<b>Comment:</b> pCerulean_Zegfr:1907 and pCerulean_6xHis_MiddleLinker were cloned and sent for sequencing yesterday.
+p50 DNA-Mix: 7,9 µl vector + 1,1 µl insert <br />
+<br />
+Transformation:
+Transformation was performed according to the standard protocol with DYT and BL21 cells. The cells were spread on the agar plates containing chloramphenicol.
+<br />
+====<p style="font-size:15px; background-color:#ff00ff;">'''Sequencing results of SalI SDM'''</p>====
+Investigator: <b>Hanna</b>
 <br/>
-<b>1. pCerulean_Zegfr:1907:</b> Sequencing looked well.
+<p style="color:#ff00ff;"><b>Comment:</b> The test digestion already showed that the SDM of the SalI restriction site in pAAV_RC worked. This could be validated by sequencing the plasmid with the Rep-1250_for primer: <br/> </p>
 <br/>
-[[File:Freiburg10 pCerulean Zegfr1907 seq.JPG|700px]]
+[[File:Freiburg10 SalI.jpg|800px]]
 <br/>
-<b>2. pCerulean_6xHis_MiddleLinker:</b> Sequencing looked also well.
-[[File:Freiburg10 pCeruelan 6xHis MiddleLinker seq.JPG|700px]]
 <br/>
-====<p style="font-size:15px; background-color:#ff00ff;"><b>Cloning of pCerulean_Zegfr:1907_"Linker" and pCerulean_CFP_MiddleLinker</b></p>====
+P58 can be used for further RepCap-experiments.
-<b>Investigator: Hanna <br /></b>
-<br/>
-<p style="color:#ff00ff;"><b>Comment:</b> For N-terminal fusion to VP2, the Affibody - fused to different kinds of linkers - will be cloned into the expression plasmid pCerulean. For imaging CFP, which was fused to the middle linker, will be cloned into pCerulean. </p> <br/>
+===83. Labortag 08.08.2010===
+HT 1080 cells were split and seeded: 3x10^6 cells per into each well of a 6-well plate.
-<p style="font-size:15px; font-weight: bold; color: #ff00ff;">Practical Cloning:</p>
+A431 cells were washed and received new medium.
+There were no clones on the agar plates so they were put back into the 37°C room. Maybe there will be some clones tomorrow.
+===84. Labortag 09.08.2010===
+====<p style="font-size:15px; background-color:#66bbff;"><b>Midi-Prep Inoculation</b></p>====
+*pAAV_RC
+*pAAV_RC_1.2 SDM SalI (P158)
+*pAAV_RC_mGMK_TK30 clone 1 (P81)
+*pAAV_RC_mGMK_TK30 clone 2 (P82)
+Investigators: Chris W., Patrick
+====<p style="font-size:15px; background-color:#66bbff;"><b>Continuation: Cloning Rep40 & Rep52 into pSB1C3</b></p>====
+<b>Investigator: Patrick </b> <br />
+Two Rep52+DMSO clones grew. They were picked and tomorrow there will be a midi prep and a test digestion.
+Simultaneously a new approach for cloning Rep40 and Rep52 into pSB1C3 was performed. (see next header)
+====<p style="font-size:15px; background-color:#66bbff;"><b>Repetition: BioBrick production of Rep40 & Rep52</b></p>====
+'''Investigator: Anna
+<p style="font-size:13px; color:#68bbff;">'''''Comments''''': Another approach was done because there were no clones for Rep 40 and only two for Rep 52 (Cloning see 06.08.2010). PCR was performed again with DMSO. Samples from gel extraction are stored in 4°C freezer. </p> <br>
+<br>
+'''PCR
-*plasmid:
-**Vector: name: pCerulean number: P273
-**Insert: name: pSB1C3_Zegfr:1907_LongLinker (P298), pSB1C3_Zegfr:1907_MiddleLinker (P290), pSB1C3_Zegfr:1907_SEG (P296), pSB1C3_Zegfr:1907_ShortLinker (P292), pSB1C3_CFP_MiddleLinker (P276)
-*new vector name: pCerulean_Zegfr:1907_"Linker" and pCerulean_CFP_MiddleLinker
-*buffer used: 4 ; Restriction-enzymes used: Enzyme 1 EcoRI-HF ; Enzyme 2 PstI-HF
-*DNA concentration (vector): 419.5 ng/µL ; DNA concentration (insert): P298 229.7 ng/µL, P290 227.4 ng/µl; P296 218.7 ng/µL; P292 196.6 ng/µL; P276 207.7  ng/µL
-<br />
-'''Comments:''' No.
-<br />
-<br />
-<p style="font-size:15px; font-weight: bold; color: #ff00ff;">Digestion</p>
 {| border="1"
-| components   || align="right" |volume of pCerulean /µl || align="right" |volume of Zegfr:1907_MiddleLinker /µl || align="right"|volume of CFP_MiddleLinker /µL
+| '''Ingredients''' || align="right" |'''Rep 40''' ||align="right"|'''Rep52'''
 |-
-| DNA  ||  align="right" | 8.3 ||  align="right" | 7.6 ||  align="right" | 4.8
+| 5X Phusion HF buffer ||  align="right" |10 µl||align="right"|10 µl
 |-
-| BSA (10x) ||  align="right" | - ||  align="right" | - ||  align="right" | -
+| 10 mM dNTP mix||  align="right" |1µl ||align="right"|1 µl
 |-
-| Buffer 4 (10x)||  align="right" | 2 ||  align="right" | 2 ||  align="right" | 2
+| forward primer: O094 ||  align="right" |2,5µl||align="right"|2,5 µl
 |-
-|Enzyme 1 EcoRI-HF||  align="right" | 1 ||  align="right" | 1 ||  align="right" | 1
+| reverse primer: O0096/ O097 ||  align="right" |2,5 µl||align="right"|2,5 µl
 |-
-|Enzyme 2 PstI-HF||  align="right" | 1 ||  align="right" | 1 ||  align="right" | 1
+| DNA Template (1ng)||  align="right" |1 µl||align="right"| 1 µl
 |-
-|H<sub>2</sub>O||  align="right" | 7.7 ||  align="right" | 8.4 ||  align="right" | 11.2
+| DMSO ||  align="right" |1 µl||align="right"|1 µl
 |-
-|'''Total volume'''||  align="right" | 20 ||  align="right" | 20 ||  align="right" | 20
+| Phusion Polymerase||  align="right" |0,5 µl||align="right"| 0,5 µl
+|-
+|H<sub>2</sub>O||  align="right" |31,5 µl||align="right"|31,5 µl
+|-
+|Total volume||  align="right" |50 µl||align="right"| 50 µl
 |}
-*Incubation: 1.5 h
+<br>
-<br /><br />
-<p style="font-size:15px; font-weight: bold; color: #ff00ff;">Agarose-Gel:</p>
+'''PCR programm
+{| border="1"
+|'''PCR Program'''|| align="right" |'''temperature/ °C'''|| align="right" |'''Time''' || align="right" |'''PCR products
+|-
+|1||  align="right" |98 ||  align="right" |1min||  align="right" |
+|-
+|2||  align="right" |98 ||  align="right" |15s||  align="right" |
+|-
+|8x||  align="right" |*** ||  align="right" |15s||  align="right" |63°C
+|-
+|3 ||  align="right" |72||  align="right" |***||  align="right" |15s
+|-
+|4 ||  align="right" |98||  align="right" | 15s||  align="right" |
+|-
+|19x||  align="right" |***||  align="right" |15s||  align="right" |68°C
+|-
+|5||  align="right" |72||  align="right" |***||  align="right" |15s
+|-
+|6x||  align="right" |72||  align="right" |5min||  align="right" |
+|-
+|Hold||  align="right" |4||  align="right" |  ||  align="right" |
+|}
+<br>
+'''Agarose gel
+.5  g Agarose, 50 mL TAE (1 %),3 µL GELRED, at 120 Volt, running time: 45 minutes
 <br />
-.8 g Agarose, 50 TAE (1.5 %), 5 µL EthBr, at 70 Volt, running time: ~ 1 hour
 <br />
+{| border="1" cellspacing="0" cellpadding="2" bordercolor="black"
+!Sample
+!Sample / µl]
+!Loading dye (6x) / µl
+!Expected size
+|--
+|p22 (Rep40)
+|44 µl
+|7 µl
+|940 bp
+|--
+|p23 (Rep52)
+|44 µl
+|7 µl
+|~1200 bp
+|--
+|}
+{| align=right
+|}
+<br />
+*Marker: GeneRuler ladder mix
+{| border="1"
+|
+!Marker /µL
+!Sample Rep40 /µl
+!Sample Rep52 /µl
+|-
+!Lane
+|7
+|51
+|51
+|-
+|}
+<br />
+[[File:Freiburg10 Rep40 Rep52.png|800px]]<br />
+'''Gel extraction<br/>
+PCR products were eluted with 20 µl BE puffer following the standard protocol.<br/>
+c(Rep40)= 28,03 ng/µl<br/>
+c(Rep52)= 121,16 ng/µl<br/>
+<p style="font-size:13px; color:#68bbff;">'''''Comments''''': Digestion was done with the wrong enzymes (EcoRI HF and SpeI), it will be repeated on 11.08. with XbaI and SpeI</p> <br>
+====<p style="font-size:15px; background-color:#66bbff;"><b>Sequence analysis of pSB1C3_mGMK</b></p>====
+Investigator: <b>Bea </B>
+<br />
+<p style="font-size:13px; color:#003399;"><b>Comments</b>: mGMK was cloned into the pSB1C3 backbone in order to send it to the parts registry!. The sequence analysis revealed that the mGMK was <b>successfully </b> cloned into pSB1C3 plasmid. This polasmid is in the RFC25 standard.</p>
+<ul>
+<b>Results sequencing: Sequence read ok! </b>
+<br />
+Primer used: VR-2
+<br />
+Comment: A mutation has been found in the pSB1C3 backone which was found generally in the backbone which we received from the iGEM HQ.
+<br />
+</ul>
+[[File:Freiburg10 Sequence analysis of pSB1C3 mGMK 09 08 2010.jpg|1000px]]
+====<p style="font-size:15px; background-color:#66bbff;"><b>Mini-Prep of pSB1C3_hTERT, pSB1C3_beta-globin_mVenus, pSB1C3_pTAV2(P5), pSB1C3_pAAV_RC(P5TATAles)</b></p>====
+<b>Investigator: Jessica</b><br>
+'''Bold text'''
+Mini-Prep following the standart Protokoll
+<br />
+<li>P177 = pSB1C3_hTERT clone1 = 163,6 ng/µl
+<li>P178 = pSB1C3_hTERT clone2 = 312,0 ng/µl
+<li>P179 = pSB1C3_betaglobin_mVenus clone1 = 237,2 ng/µl
+<li>P180 = pSB1C3_betaglobin_mVenus clone2 = 228,2 ng/µl
+<li>P181 = pSB1C3_pTAV2(P5) clone1 = 108,8ng/µl
+<li>P181 = pSB1C3_pTAV2(P5) clone2 = 140,9 ng/µl
+<li>P181 = pSB1C3_pAAV_RC(P5TATAless) clone1 = 165,0 ng/µl
+<li>P181 = pSB1C3_pAAV_RC(P5TATAless) clone2 = 176,6 ng/µl
+<li>P181 = pSB1C3_pAAV_RC(P5TATAless) clone3 = 176,9 ng/µl
+<br />
+<br>
+<br>
+<b>Test digestion:</b>
+<ul>
+<li>Perfomed with 10 µL of total volume with all 9 clones</li>
+<table border=1 cellpadding=0 cellspacing=0 width=621 style='border-collapse:
+ collapse;table-layout:fixed;width:466pt'>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt'>
+  <td height=29 class=xl6724191 width=143 style='height:21.75pt;width:107pt'>&nbsp;</td>
+  <td class=xl6824191 width=131 style='border-left:none;width:98pt'>Mastermix/µL</td>
+  <td class=xl6824191 width=87 style='border-left:none;width:65pt'>P176/µL</td>
+  <td class=xl6824191 width=84 style='border-left:none;width:63pt'>P177/µL</td>
+  <td class=xl6824191 width=90 style='border-left:none;width:68pt'>P178/µL</td>
+  <td class=xl6824191 width=86 style='border-left:none;width:65pt'>P179/µL</td>
+  <td class=xl6824191 width=86 style='border-left:none;width:65pt'>P180/µL</td>
+  <td class=xl6824191 width=86 style='border-left:none;width:65pt'>P181/µL</td>
+  <td class=xl6824191 width=86 style='border-left:none;width:65pt'>P182/µL</td>
+  <td class=xl6824191 width=86 style='border-left:none;width:65pt'>P183/µL</td>
+  <td class=xl6824191 width=86 style='border-left:none;width:65pt'>P184/µL</td>
+ </tr>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt'>
+  <td height=29 class=xl6624191 width=143 style='height:21.75pt;border-top:
+  none;width:107pt'><span lang=EN-US style='mso-ansi-language:EN-US'>DNA</span></td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>-</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>4,3</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>2,3</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>3,0</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>2,4</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>6,4</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>5,0</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>4,2</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>4,0</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>4,0</td>
+ </tr>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt;mso-yfti-irow:
+'>
+  <td height=29 class=xl6624191 width=143 style='height:21.75pt;border-top:
+  none;width:107pt'><span lang=EN-US style='mso-ansi-language:EN-US'>BSA (10x)</span></td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>10</td>
+  <td rowspan=4 class=xl6524191 style='border-top:none'>3</td>
+  <td rowspan=4 class=xl6524191 style='border-top:none'>3</td>
+  <td rowspan=4 class=xl6524191 style='border-top:none'>3</td>
+  <td rowspan=4 class=xl6524191 style='border-top:none'>3</td>
+  <td rowspan=4 class=xl6524191 style='border-top:none'>3</td>
+  <td rowspan=4 class=xl6524191 style='border-top:none'>3</td>
+  <td rowspan=4 class=xl6524191 style='border-top:none'>3</td>
+  <td rowspan=4 class=xl6524191 style='border-top:none'>3</td>
+  <td rowspan=4 class=xl6524191 style='border-top:none'>3</td>
+ </tr>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt;mso-yfti-irow:
+'>
+  <td height=29 class=xl6624191 width=143 style='height:21.75pt;border-top:
+  none;width:107pt'><span lang=EN-US style='mso-ansi-language:EN-US'>Buffer
+<span style='mso-spacerun:yes'>   </span>(10x)</span></td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>10</td>
+ </tr>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt;mso-yfti-irow:
+'>
+  <td height=29 class=xl6624191 width=143 style='height:21.75pt;border-top:
+  none;width:107pt'><span lang=EN-US style='mso-ansi-language:EN-US'>Enzyme
+  XbaI<span style='mso-spacerun:yes'> </span></span></td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>5</td>
+ </tr>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt;mso-yfti-irow:
+'>
+  <td height=29 class=xl6624191 width=143 style='height:21.75pt;border-top:
+  none;width:107pt'><span lang=EN-US style='mso-ansi-language:EN-US'>Enzyme
+  AgeI</span></td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>5</td>
+ </tr>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt;mso-yfti-irow:
+;mso-yfti-lastrow:yes'>
+  <td height=29 class=xl6624191 width=143 style='height:21.75pt;border-top:
+  none;width:107pt'><span lang=EN-US style='mso-ansi-language:EN-US'>H2O</span></td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>-</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>2,7</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>4,7</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>4,0</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>4,6</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>0,6</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>2,0</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>2,8</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>3,0</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>3,0</td>
+ </tr>
+ <tr height=29 style='mso-height-source:userset;height:21.75pt'>
+  <td height=29 class=xl6624191 width=143 style='height:21.75pt;border-top:
+  none;width:107pt'>Total volume</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>30</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>10</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>10</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>10</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>10</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>10</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>10</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>10</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>10</td>
+  <td class=xl6524191 style='border-top:none;border-left:none'>10</td>
+ </tr>
+ <tr height=0 style='display:none'>
+  <td width=143 style='width:107pt'></td>
+  <td width=131 style='width:98pt'></td>
+  <td width=87 style='width:65pt'></td>
+  <td width=84 style='width:63pt'></td>
+  <td width=90 style='width:68pt'></td>
+  <td width=86 style='width:65pt'></td>
+ </tr>
+</table>
+<br />
+</ul>
+<ul>
+<li>All 9 samples were loaded on a 1% agarose gel</li>
+<li>P176 = pSB1C3_hTERT clone1 </li>
+<li>P177 = pSB1C3_hTERT clone2 </li>
+<li>P178 = pSB1C3_betaglobin clone1</li>
+<li>P179 = pSB1C3_betaglobin clone2</li>
+<li>P180 = pSB1C3_pTAV2(P5) clone1</li>
+<li>P181 = pSB1C3_pTAV2(P5) clone2</li>
+<li>P182 = pSB1C3_pAAV_RC(P5TATAless) clone1</li>
+<li>P183 = pSB1C3_pAAV_RC(P5TATAless) clone2</li>
+<li>P184 = pSB1C3_pAAV_RC(P5TATAless) clone3</li>
+</ul>
 <br />
 {| border="1" cellspacing="0" cellpadding="2" bordercolor="black"
@@ Line 621: / Line 2,654: @@
 !Sample/µl]
 !Loading dye (6x)/µl
-!Expected size 1
+!Expected size 1 (Geneious)
 |--
-|P273
+|P176
-|20 µl
+|10 µl
-|4 µl
+|1,6 µl
-|3922 bp
+|474 bp
 |--
-|P298
+|P177
-|20 µl
+|10 µl
-|4 µl
+|1,6 µl
-|273 bp
+|474 bp
 |--
-|P290
+|P178
-|20 µl
+|10 µl
-|4 µl
+|1,6 µl
-|261 bp
+|509 bp
 |--
-|P296
+|P179
-|20 µl
+|10 µl
-|4 µl
+|1,6 µl
-|345 bp
+|509 bp
 |--
-|P292
+|P1780
-|20 µl
+|10 µl
-|4 µl
+|1,6 µl
-|249 bp
+|164 bp
 |--
-|P276
+|P181
-|20 µl
+|10 µl
-|4 µl
+|1,6 µl
-|801 bp
+|164 bp
 |--
+|P182
+|10 µl
+|1,6 µl
+|164 bp
+|--
+|P183
+|10 µl
+|1,6 µl
+|164 bp
+|--
+|P184
+|10 µl
+|1,6 µl
+|164 bp
+|--
 |}
 {| align=right
 |}
+[[File:9 Proben tert, beta, p5.jpg|400px]]
+<br />
+<br />
+<p style="font-size:13px; color:#66bbff;"><b>Comments:</b> hTERT and betaglobin_mVenus is inserted in pSB1C3, pTAV(P5) and pAAV_RC (P5TATAless) will be sequenced</p><br>
+Primer: Reverse Primer VR2
+====<p style="font-size:15px; background-color:#66bbff;"><b>Cell culture</b></p>====
+Investigators: Adrian, Kerstin, Patrick
+<br />
+=====Transfection on HEK293=====
+<br />
+The motivation: first we want to create new stock of AAV without GOI, the next viral stock is with correct TK/GMK, the last stocks are with different YFP-amounts to check if the amount of GOI is a critical step for transduction effency (transgene expression).
 <br />
-*Marker: GeneRuler ladder mix
 {| border="1"
-|
+| Plate  || align="right"  |pAAV_RC/µg|| align="right" |pHelper/µg|| align="right" |GOI/µg
-!Marker
-!Sample P273 /µl
-!Sample P276 /µl
-!Sample P290 /µl
-!Sample P292 /µl
-!Sample P296 /µl
-!Sample P298 /µl
 |-
-!Lane
+| 1||  align="right" |3,3 ||  align="right" | 3,3||  align="right" | no GOI
-|5
+|-
-|24
+| 2||  align="right" |6,6 ||  align="right" | 3,3||  align="right" | no GOI
-|24
+|-
-|24
+| 3||  align="right" |3,3 ||  align="right" | 3,3||  align="right" | 3,3 TK_GMK clone1
-|24
+|-
-|24
+| 4||  align="right" |3,3 ||  align="right" | 3,3||  align="right" | 3,3 TK_GMK clone1
-|24
+|-
+| 5||  align="right" |3,3 ||  align="right" | 3,3||  align="right" | 3,3 TK_GMK clone2
+|-
+| 6||  align="right" |3,3 ||  align="right" | 3,3||  align="right" | 3,3 YFP
+|-
+| 7||  align="right" |3,3 ||  align="right" | 3,3||  align="right" | 10 YFP
+|-
+| 8||  align="right" |3,3 ||  align="right" | 3,3||  align="right" | 20 YFP
+|-
+| 9||  align="right" |3,3 ||  align="right" | 3,3||  align="right" | 40 YFP
+|-
+| 10|| align="right" |3,3 ||  align="right" | 3,3||  align="right" | 60 YFP
 |-
 |}
+=====Transduction of HT1080=====
+<br />Motivation
+The Motivation: checking survivalrate of Cells, with either no Virus, virus without GOI and virus with YFP (10µg stock)<br />
+The Plan: <br />
+Plate I
+{| border="1"
+| control, no cells || align="right" |no GOI 150µl|| align="right" |10µg 500µl|
+|-
+| control, no virus||  align="right" |no GOI 300µl||  align="right" | 10µg 750µl|
+|-
+|}
+Plate II
+{| border="1"
+| control, no cells || align="right" |no GOI 150µl|| align="right" |10µg 500µl|
+|-
+| control, no virus||  align="right" |no GOI 300µl||  align="right" | 10µg 750µl|
+|-
+|}
+Plate III
+{| border="1"
+| control, no cells || align="right" |no GOI 150µl|| align="right" |10µg 500µl|
+|-
+| control, no virus||  align="right" |no virus||  align="right" | 10µg 750µl|
+|-
+|}
+=====Passaging and seeding of A431=====
+one 6er dish was prepared for making pictures and one T75 Flask.
 <br />
+====<p style="font-size:15px; background-color:#66bbff;"><b>BioBrick Assembly of pSB1C3_leftITR_CMV and pSB1C3_hGH_rightITR</b></p>====
+Investigator: <b>Bea, Achim, Jo</B>
+<br />
+<p style="font-size:13px; color:#003399;"><b>Comments</b>: In order to proceed with the BioBrick assembly the pasmids pSB1C3_left ITR and pSB1C3_CMV were used and pSB1C3_rigthITR and pSB1C3_hGH were used in order to obatin plasmids with both sequences.</p>
+<gallery widths=400px heights=400px perrow=2 caption="BioBrick assembly of pSB1C3_hGH_rightITR and pSB1C3_leftITR_CMV">
+Image:Freiburg10 BioBrick assembbly of pSB1C3 leftITR CMV 09 08 2010.JPG|Cloning strategy of pSB1C3_leftITR CMV
+Image:Freiburg10 BioBrick assembbly of pSB1C3 hGH rightITR 09 08 2010.jpg|pSB1C3_hGH_rightITR
+</gallery>
-<p style="font-size:15px; font-weight: bold; color: #ff00ff;">Gel extraction</p>
 <br />
-Gel measurement:
 <br />
+<b>Digestion:</b> <br />
 {| border="1"
-| align="left" | '''Sample'''
+| '''components'''   || align="right" |'''pSB1C3_left ITR''' || align="right" |'''pSB1C3_CMV''' || align="right" |'''pSB1C3_right ITR''' || align="right" |''' pSB1C3_hGH'''
-| align="left" | '''Volume'''
-| align="left" | '''Concentration'''
 |-
-| align="left" | P273
+| DNA  ||  align="right" |13,4 ||  align="right" |9,5 ||  align="right" |13,6 ||  align="right" |6,6
-| align="left" | 20
-| align="left" | 115.45 ng/µL
 |-
-| align="left" | P276
+| BSA (10x) ||  align="right" |2 ||  align="right" | 2 ||  align="right" |2 ||  align="right" | 2
-| align="left" | 20
-| align="left" | 9.91 ng/µL
 |-
-| align="left" | P298
+| Buffer 4 (10x)||  align="right" |2 ||  align="right" |2 ||  align="right" |2 ||  align="right" | 2
-| align="left" | 20
-| align="left" | 5.07 ng/µL
 |-
-| align="left" | P296
+|Enzyme1 ||  align="right" |1 (SpeI) ||  align="right" |1 (Xba1)||  align="right" |1 (EcoRI) ||  align="right" |1 (EcoRI)
-| align="left" | 20
-| align="left" | 9.03 ng/µL
 |-
-| align="left" | P290
+|Enzyme2 ||  align="right" |1 (PstI)||  align="right" |1 (PstI) ||  align="right" |1 (XbaI)||  align="right" |1 (SpeI)
-| align="left" | 20
-| align="left" | 10.31 ng/µL
 |-
-| align="left" | P292
+|H2O||  align="right" |0,6 ||  align="right" |4,5 ||  align="right" |0,4 ||  align="right" |7,4
-| align="left" | 20
+|-
-| align="left" | 20.78 ng/µL
+|'''Total volume'''||  align="right" | 20||  align="right" |20 ||  align="right" | 20||  align="right" |20
 |}
-<br /><br />
+<br />
+Preparation of gel:<br />
+,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 115 Volt, running time: 45 minutes
+<br />
-<p style="font-size:15px; font-weight: bold; color: #ff00ff;">Ligation</p>
+[[Image: Freiburg10 9 8 2010 Digestion of psB1C3 rITR psB1C3 lITR psB1C3 CMV psB1C3 hGH125.jpg|200px]]
+<p style="font-size:13px; color:#ff00ff;"><b>Oh, nice picture.. I can recognize many details :)*g* (Hanna) </b> </p>
+Expected sizes of constructs:
+*pSB1C3_CMV:  650 bp
+*pSB1C3_lITR: 2200 bp
+*pSB1C3_hGH:  500 bp
+*pSB1C3_rITR: 2200 bp
+The correspnding bands were cut out and Gel-Extraction was performed according to protocol.
 <br />
-<b>1. PCerulean_Zegfr:1907_LongLinker</b>
+<br />
+concentrations measured via NanoDrop:
+*pSB1C3_CMV:  13,51 ng/µl
+*pSB1C3_lITR: 18,49  ng/µl
+*pSB1C3_hGH:  7,22  ng/µl
+*pSB1C3_rITR: 20,24  ng/µl
+<br />
+<b>Ligation:</b> <br />
+For ligation, T4 ligase was used.
+<br />
+* 1µl T4-Ligase buffer (10x)
+* 8µl (Vector + Insert) mix
+* 1µl T4-Ligase
+Ligation was carried out as following:
+* Ligation 1:
+**pSB1C3_CMV:  4,4 ng/µl
+**pSB1C3_lITR: 3,6  ng/µl
+*Ligation 2:
+**pSB1C3_hGH:  5,25 µl
+**pSB1C3_rITR: 2,75 µl
+<br /> Incubation for 40 minutes.
+<br />
+<b>Transformation:</b><br />
+Transformation carried out according to standard protocol (BL21). Cells were plated on an agar plate with chloramphenicol.
+<br />
+====<p style="font-size:15px; background-color:#66bbff;"><b>Repetition: Cloning of SDM SspI and SDM PvuII</b></p>====
+Investigator: <b>Stefan</B><br />
+<p style="color:red;">Comments: Last week's cloning of SDM_SspI and SDM_PvuII didn't work out, so this is the repetition. In this approach the same restriction enzymes and amounts of DNA were used.</p> <br />
+<br />
+*Vector: name: pSB1C3_SDM_SspI <b>P125</b>
+*Insert: name: pSB1C3_SDM_PvuII <b>P129</b>
+*buffer used: 4
+*Restriction-enzymes used:
+**BpmI (no. Lab: 144)
+**ClaI (no.Lab: 152)
+*DNA concentration (P125): 321,9 ng/µl
+*DNA concentration (P129): 308,4 ng/µl
+<br />
+<b>Digestion:</b> <br />
 {| border="1"
-| align="left" |  ||align="left"| '''P298''' ||align="left"| '''P273'''
+| '''components'''   || align="right" |'''volume of pSB1C3_SDM_SspI /µl''' || align="right" |'''volume of pSB1C3_SDm_PvuII /µl'''
+|-
+| DNA  ||  align="right" |4,66 ||  align="right" |4,87
+|-
+| BSA (10x) ||  align="right" |2 ||  align="right" | 2
+|-
+| Buffer 4 (10x)||  align="right" |2 ||  align="right" |2
+|-
+|BpmI (no.Lab:144)||  align="right" |1 ||  align="right" |1
+|-
+|ClaI (no.Lab:152)||  align="right" |1 ||  align="right" |1
+|-
+|H2O||  align="right" |9,34 ||  align="right" |9,13
 |-
-| align="left" | '''Volume/µl''' ||align="left"| 6.61 ||align="left"| 1.39
+|'''Total volume'''||  align="right" | 20||  align="right" |20
 |}
 <br />
-<b>2. PCerulean_Zegfr:1907_MiddleLinker</b>
+<b>Gel extraction:</b> <br />
+Preparation of gel:<br />
+,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 115 Volt, running time: 45 minutes
+<br />
+Expected sizes of constructs:
+*pSB1C3_SDM_SspI: 1819 bp
+*pSB1C3_SDM_PvuII: 981 bp
+The correspnding bands were cut out and Gel-Extraction was performed according to protocol.
+<br />
+[[File:Freiburg10 pSB1C3 SDM SspI and PvuII 090810.png|500px|left|thumb|]]<br />
+<br />
+concentrations measured via NanoDrop:
+* Sspl: 19,85 ng/µl
+* PvuII: 10,57 ng/µl
+<br />
+<b>Ligation:</b> <br />
+For ligation, T4 ligase was used.
+<br />
+* 1µl T4-Ligase buffer (10x)
+* 8µl (Vector + Insert) mix
+* 1µl T4-Ligase
+The Ligation was performed as following:
+* SDM_SspI Volume: 4,03 µl
+* SDM_PvuII Volume: 3,97 µl
+<br />
+* 1µl T4-Ligase buffer (10x)
+* 8µl (Vector + Insert) mix
+* 1µl T4-Ligase
+<br /> Incubating for 45 minutes.
+<br />
+<b>Transformation:</b><br />
+Transformation performed according to the standard protocol (BL21). The cells were plated on a agar plate with chloramphenicol.
+<br />
+====<p style="font-size:15px; background-color:#ff00ff;"><b>Design and ordering of primer for P40 Promoter BioBrick production</b></p>====
+Investigator: <b>Hanna</B><br />
+<br/>
+In order to generate a P40 promoter BioBrick = "Cap-Promoter", oligos were designed and ordered at Sigma Aldrich:<br/>
+[[File:Freiburg10 P40.jpg|450px]]
+<br/>
+=== 85. labday 10.08.2010===
+====<p style="font-size:15px; background-color:#66bbff;"><b>Retrafo with RepCap gene (Mr.Gene)</b></p>====
+<b>Investigator: Bea</b><br>
+<p style="font-size:13px; color:#66bbff;"><b>Comments</b>: We received the rep_cap insert ordered from Mr. Gene today. In order to used and clone the insert into the desired sequences a retrafo has to be performed.   </p>
+<b> Re-transformation: </b>
+<ul>
+<li>Construct used: pMA_REP_CAP</li>
+<li> We reveived 5 µg (lyophilzied). These were resuspended in 100 µL H<sub>2</sub>O and vortexted.</li>
+<li>c = 50 ng/µL</li>
+<li>c = Plasmid need to be diluted in order to obatain the final 500pg</li>
+<li>Dilution: 1:100</li>
+<li>100 µL aliquot of <b>XL1-B</b> were thawed on ice. The proper amount of 1µL was added to the cells.</li>
+<li>Transformed cells were plated on LB plates containing ampicillin</li>
+</ul>
+====<p style="font-size:15px; background-color:#66bbff;"><b>Continuation: Cloning Rep40 & Rep52 into pSB1C3</b></p>====
+A midi prep of the two Rep52+DMSO clones was performed yielding concentrations of 261,35 ng/µl (clone 1) and 240,47 ng/µl (clone 2). Unfortunately we noticed today that we should not use EcoRI to clone Rep52 into pSB1C3 because EcoRI cuts two times within the sequence of Rep52.
+====<p style="font-size:15px; background-color:#66bbff;"><b>Midi-Prep of pAAV_RC, pAAV_RC_1.2 SDM SalI (P158), pAAV_RFC25_mGMK_TK30 clone 1 (P81) and 2 (P82)</b></p>====
+Investigators: Patrick, Chris <br>
+The Midi-Preps were performed according to the standard protocol yielding the following concentrations:
 {| border="1"
-| align="left" |  ||align="left"| '''P290''' ||align="left"| '''P273'''
+| pAAV_RC || align="right" |P81a|| align="right" |P81b|| align="right" |P82a|| align="right" |P82b|| align="right" |P158a|| align="right" |P158b
+|-
+| 1348,49 ng/µl||  align="right" |1783,86 ng/µl||  align="right" | 2096,25 ng/µl|| align="right" |1915 ng/µl|| align="right" |1469,35 ng/µl|| align="right" |1834,25 ng/µl|| align="right" |1771,27 ng/µl
 |-
-| align="left" | '''Volume/µl''' ||align="left"| 5.53 ||align="left"| 2.47
 |}
+<br>
+The annotations a and b were added because two midi-preps of P81, P82 and P158 were carried out.
+====<p style="font-size:15px; background-color:#66bbff;"><b>Results of sequencing pSB1C3_pTAV2(P5) and Psb1C3_pAAV_RC(P5TATAless)</b></p>====
+<b>Investigator: Jessica</b><br>
+[[image:mistake.png|thumb|right]]
+@Jessi: Which clones are ok, which not?? text does not correspond to pictures! (Bea)
 <br />
-<b>3. PCerulean_Zegfr:1907_SEG</b>
+[[File:Freiburg10_Sequence_alignment_P5 mit TATA clone1neu.jpg|500px|left|thumb|]]
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+sequencing of '''P180''' was successful, P5 with TATAbox is in pSB1C3
+[[File:Freiburg10_Sequence_alignment_P5TATAless clone2neu.jpg|500px|left|thumb|]]
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+sequencing of '''P183''' was successful but there is a G missing --> plamid is thrown away
+[[File:Freiburg10_Sequence_alignment_P5TATAless clone3.jpg|500px|left|thumb|]]
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+sequencing of '''P184''' was successful, P5 is in without TATAbox. this plasmid can be used. <br>
+<br>
+'''P181''' and '''P180''' are thrown away because of the result of the test digestion.
+====<p style="font-size:15px; background-color:#66bbff;"><b>Repetition: BioBrick production of Rep40 and Rep 52</b></p>====
+Investigator: <b>Anna</B><br />
+<p style="font-size:13px; color:#68bbff;">'''''Comments''''': PCR was repeated once again (that was bad!), because digestion was done with the wrong enzymes (EcoRI HF and SpeI). There are some differences in the PCR programm in comparison to the last (see 09.10.)</p> <br>
+<br>
+'''PCR
 {| border="1"
-| align="left" |  ||align="left"| '''P296''' ||align="left"| '''P273'''
+| '''Ingredients''' || align="right" |'''Rep 40''' ||align="right"|'''Rep52'''
+|-
+| 5X Phusion HF buffer ||  align="right" |10 µl||align="right"|10 µl
+|-
+| 10 mM dNTP mix||  align="right" |1µl ||align="right"|1 µl
+|-
+| forward primer: O094 ||  align="right" |2,5µl||align="right"|2,5 µl
+|-
+| reverse primer: O0096/ O097 ||  align="right" |2,5 µl||align="right"|2,5 µl
+|-
+| DNA Template 1:100 (1ng)||  align="right" |1 µl||align="right"| 1 µl
+|-
+| DMSO ||  align="right" |1 µl||align="right"|1 µl
+|-
+| Phusion Polymerase||  align="right" |0,5 µl||align="right"| 0,5 µl
+|-
+|H<sub>2</sub>O||  align="right" |31,5 µl||align="right"|31,5 µl
 |-
-| align="left" | '''Volume/µl''' ||align="left"| 6.17 ||align="left"| 1.83
+|Total volume||  align="right" |50 µl||align="right"| 50 µl
 |}
-<br />
+<br>
-<b>4. PCerulean_Zegfr:1907_ShortLinker</b>
+'''PCR programm
 {| border="1"
-| align="left" |  ||align="left"| '''P292''' ||align="left"| '''P273'''
+|'''PCR Program'''|| align="right" |'''temperature/ °C'''|| align="right" |'''Time''' || align="right" |'''PCR products
 |-
-| align="left" | '''Volume/µl''' ||align="left"| 4.11 ||align="left"| 3.89
+|1||  align="right" |98 ||  align="right" |1min||  align="right" |
+|-
+|2||  align="right" |98 ||  align="right" |15s||  align="right" |
+|-
+|8x||  align="right" |*** ||  align="right" |15s||  align="right" |'''62,5°C
+|-
+|3 ||  align="right" |72||  align="right" |***||  align="right" |'''25s
+|-
+|4 ||  align="right" |98||  align="right" | 15s||  align="right" |
+|-
+|19x||  align="right" |***||  align="right" |15s||  align="right" |'''67°C
+|-
+|5||  align="right" |72||  align="right" |***||  align="right" |'''25s
+|-
+|6x||  align="right" |72||  align="right" |5min||  align="right" |
+|-
+|Hold||  align="right" |4||  align="right" |  ||  align="right" |
 |}
+<br>
+'''Agarose gel
+.5  g Agarose, 50 mL TAE (1 %),3 µL GELRED, at 120 Volt, running time: 45 minutes
 <br />
-<b>5. PCerulean_CFP_MiddleLinker</b>
+<br />
+{| border="1" cellspacing="0" cellpadding="2" bordercolor="black"
+!Sample
+!Sample / µl]
+!Loading dye (6x) / µl
+!Expected size
+|--
+|p22 (Rep40)
+|50 µl
+|8 µl
+|940 bp
+|--
+|p23 (Rep52)
+|50 µl
+|8 µl
+|~1200 bp
+|--
+|}
+{| align=right
+|}
+<br />
+*Marker: GeneRuler ladder mix
 {| border="1"
-| align="left" |  ||align="left"| '''P276''' ||align="left"| '''P273'''
+|
+!Marker /µL
+!Sample Rep40 /µl
+!Sample Rep52 /µl
+|-
+!Lane
+|7
+|58
+|58
 |-
-| align="left" | '''Volume/µl''' ||align="left"| 7.02 ||align="left"| 0.98
 |}
 <br />
-<p style="font-size:15px; font-weight: bold; color: #ff00ff;">Trafo</p>
+[[File:Freiburg10_Rep40_52.jpg|500px|left|thumb|]]
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
 <br />
-Trafo was performed following the standard protocol. Used cells: XL1b, DNA amount: 2.5 µL of each ligation reaction. Plates were stored @ 37°C room over night.
+<p style="font-size:13px; color:#68bbff;">'''''Comments''''': Digestion of the samples will be done tomorrow with XbaI and SpeI.</p> <br>
-<br/>
+<br />
-====<p style="font-size:15px; background-color:#66bbff;"><b>Harvest viral particles, Seeding HT1080 cells</b></p>====
+'''Gelextraction
-<b>Investigator: Adrian, Kerstin <br /></b>
-*Harvest viral particles of Transfection from 31.08.2010 (six approaches: 10µg of RC (2x P326 and 2x P325 and 2x Stratagene), pHelper and GOI (P262))
+Elution was done with 20 µl Pe buffer following the standard protocol.<br />
-*Seeding HT1080 cells
-====<p style="font-size:15px; background-color:#66bbff;"><b>Continuation: Cloning CFP_middlelinker (from pSB1C3_CFP_middlelinker, P276) into pCerulean (P273)</b></p>====
+c(Rep40)= 23,1 ng/µl<br />
-Investigator: Patrick
+c(Rep52)= 78,0 ng/µl
-<br />
+====<p style="font-size:15px; background-color:#66bbff;"><b>Preparation of competent XL1blue and testtrafo</b></p>====
-The Miniprep was performed according to the standard protocol.
+<b>Investigator: Jessica</b><br>
-Labelling:
+preparation of competent E.coli XL1blue was made according to the standardprotocol (91 eppis with '''60µl''') they are in the green boxes in -80°C<br>
-*P381: pCerulean_middlelinker clone 1 upper band : 526,0 ng/µl
+testtrafo was made
-*P382: pCerulean_middlelinker clone 2 upper band : 522,0 ng/µl
+<ul><li>one plate with 50pg/µl</li>
-*P383: pCerulean_middlelinker clone 3 upper band : 463,0 ng/µl
+<li>one plate with 100pg/µl</li>
-*P384: pCerulean_middlelinker clone 1 lower band : 465,0 ng/µl
+</ul>
-*P385: pCerulean_middlelinker clone 2 lower band : 500,0 ng/µl
+...trafo is failed because amp was missing on the plates (resistence in pUC). trafo will be repeated on aug 11th by Tobi...
-*P386: pCerulean_middlelinker clone 3 lower band : 524,0 ng/µl
-[[File:Cartoons48.jpg|thumb|right| Öhm Patrick: Hier ist der Grund, warum das Experiment "wiederholt" wurde: Falsche Beschrieftung hier, als auch in der Excel Tabelle ;) "Finde den Fehler!" :P]]
+====<p style="font-size:15px; background-color:#66bbff;"><b>Repetition: Mini-Prep and test digestion of pSB1C3_SDM_SspI/PvuII</b></p>====
+'''Investigator: Adrian, Stefan'''<br>
 <br>
+<p style="font-size:18px; font-weight: bold; color:#66bbff;"><u>Plasmid Mini-Prep</u></p>
+*vector name: pSB1C3_SDM_SspI/PvuII
+<br />
+<u>Glycerol Stocks</u> <br>
+pSB1C3_SDM_SspI/PvuII
+Only clone 1 grew, therefore there is just one stock = B159
+<p style="font-size:15px; font-weight: bold; color:#66bbff;">Test digestion</p>
+*buffer used: 2
+*Restriction-enzymes used:
+**Enzyme 1 SspI
+**Enzyme 2 PvuII
+*Plasmid: pSB1C3_SDM_SspI/PvuII:
+**Plasmid-Number: P185; DNA concentration: 47,9 ng/µL <br />
+<p style="font-size:13px; color:#ff0000;">comment: DNA was eluted into previously used tube, therefore contamination is possible.</p> <br>
+<br />
+{| border="1"
+| align="left" | '''Components''' ||align="left"| <b>P185</b> Volume/µL ||align="left"| <b>P51.1</b> Volume/µL
+|-
+| align="left" | DNA ||align="left"| 18,1 ||align="left"| 6,8
+|-
+| align="left" | BSA (10x) ||align="left"| 2,5 ||align="left"| 2,5
+|-
+| align="left" | Buffer no. 2 (10x) ||align="left"| 2,5 ||align="left"| 2,5
+|-
+| align="left" | Enzyme 1 SspI ||align="left"| 0.5 ||align="left"| 0.5
+|-
+| align="left" | Enzyme 2 PvuII ||align="left"| 0.5 ||align="left"| 0.5
+|-
+| align="left" | H<sub>2</sub>O ||align="left"| 0,9 ||align="left"| 12,2
+|-
+| align="left" | '''Total volume''' ||align="left"| <b>10</b>  ||align="left"| <b>10</b> |
+|}
+<br />
+*Incubation: 45 min
+<br />
+<p style="font-size:15px; font-weight: bold; color:#66bbff;">Agarose-Gel:</p>
+<br />
+.4 g Agarose, 50 mL <b>TAE</b>, 3 µL GELRED, at 115 Volt, running time: 45 minutes
+<br />
+{| align=right
+|}
+<br />
+*Marker: GeneRuler ladder mix
+{| border="1"
+|
+!Marker /µL
+!Sample P185 /µL
+!Sample P51.1 /µL
+|-
+!Lane
+|7
+|17
+|17
+|-
+|}
+<br />
-see also http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/index.php/August_2010#Cloning_CFP_middlelinker_.28from_pSB1C3_CFP_middlelinker.2C_P276.29_into_pCerulean_.28P273.29
+One cut is expected (PvuII in CFP).<br>
-[[File:Mistake.png|thumb|right|400px| ;-) bitte ausfüllen]]
+[[File:Freiburg10 SspI PvuII test digestion.png|300px]] <br>
-Testdigestion: 7 µl DNA sample, 1 µl Buffer 4 (10x), 1 µl BSA, 0,5 µl Xba, 0,5 µl PstI-HF
 <br>
-Expected size of the fragments: 786 & 2053bp
+<b>Comment: There are 6 bands now. This test digestion again looks very different from that of P157.2 done by Jessica (lab day 82). Results should be discussed tomorrow.</b><br>
-<br>
-There seems to be something wrong.
 <br>
-[[File:Freiburg10_pat20100903.jpg‎|400px]]
+<br/>
+<br/>
-Sent for sequencing: P381 & P385
-Labelling: P381-CMV_rev & P385-CMV_rev <br>
-Used primer: O21 : CMV_reverse_qPCR
-====<p style="font-size:15px; background-color:#66bbff;"><b>Cloning of pSB1C3_leftITR_pTert and pSB1C3_mGMK with pSB1C3_leftITR_CMV</b></p>====
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Picking clones of pSB1C3_SDM_SspI/PvuII</b></p>====
-<b>Investigator: Chris L. <br /></b>
+<p><b>Investigator: Stefan</b></p>
+<p style="font-size:13px; color:#66bbff;"><b>Comments:</b> Test digestion didn't work out, three additional clones were picked from the plate we get from yesterday's Trafo to retry tomorrow.</p>
+<ul>
+<li>Bacterial strain used: BL21</li>
+<li>Inoculating of 10 mL DYT medium containing 10µL chloramphenicol</li>
+<li> Put in 37°C room on shaker at 20.45hours.</li>
+</ul><br><br>
-*Vector: name: pSB1C3_leftITR_pTERT clone 1 '''P256''' c=179,2 ng/µl
+=== 86. labday 11.08.2010===
-*Vector: name: pSB1C3_leftITR_CMV '''P188''' c=231,6 ng/µl
+====<p style="font-size:15px; background-color:#66bbff;"><b>Biobrick Assembly:Picking Clones, Miniprep, Testdigestion of CMV&lITR/ hGH & rITR</b></p>====
-*Insert: name: pSB1C3_mGMK '''P195''' c=258,6 ng/µl
+Investigator: <b>Chris L., Achim</B>
-*new vector name: pSB1C3_leftITR_CMV_GMK
+Test Digestion showed that the cloning was succesful.
-*new vector name: pSB1C3_leftITR_pTERT_GMK
+[[Image:Freiburg10_assembly1.jpg]]
-*buffer used: 4 ; Restriction-enzymes used: Enzyme 1 PstI ; Enzyme 2 SpeI ; Enzyme 3 XbaI
+<br />
+<br />
+NanoDrop concentrations:
+*hGH_rITR1:105,15 ng/µl
+*hGH_rITR2:96.97 ng/µl
+*CMV_lITR1:231.61 ng/µl
+*CMV_lITR2:129.19 ng/µl
+<br />
+====<p style="font-size:15px; background-color:#66bbff;"><b>Biobrick Assembly: bSB1C3_lITR_CMV & pSB1C3_betaglobin_mVenus</b></p>====
+Investigator: <b>Chris L., Achim</B>
+<br />
+<p style="font-size:13px; color:#003399;"><b>Comments</b>: In order to proceed with the BioBrick assembly the plasmids pSB1C3_leftITR_CMV was cut with SpeI and PstI, pSB1C3_betaglobin_mVenus was cut with XbaI and PstI. The insert fragment containing betaglobin_mVenus was ligated to the vector fragment containing the leftITR_CMV promotor.</p>
+<br />
 <br />
+<b>Digestion:</b> <br />
 {| border="1"
-| '''components'''   || align="right" |'''P195''' || align="right" |'''P256 /µl''' || align="right" |'''P188 /µl'''
+| '''components'''   || align="right" |'''pSB1C3_leftITR_CMV''' || align="right" |'''pSB1C3_betaglobin_mVenus'''
 |-
-| DNA  ||  align="right" | 7,7 ||  align="right" | 11,2 ||  align="right" | 8,6
+| DNA  ||  align="right" |5,2 ||  align="right" |8,4
 |-
-| BSA (10x) ||  align="right" | 2 ||  align="right" | 2 ||  align="right" | 2
+| BSA (10x) ||  align="right" |2 ||  align="right" | 2
 |-
-| Buffer 4 (10x)||  align="right" |2 ||  align="right" |2 ||  align="right" |2
+| Buffer 4 (10x)||  align="right" |2 ||  align="right" |2
 |-
-|Enzyme SpeI ||  align="right" |1 ||  align="right" |1 ||  align="right" |0
+|Enzyme1 ||  align="right" |1 (SpeI) ||  align="right" |1 (Xba1)
 |-
-|Enzyme XbaI ||  align="right" |0 ||  align="right" |0 ||  align="right" |1
+|Enzyme2 ||  align="right" |1 (PstI)||  align="right" |1 (PstI)
 |-
-|Enzyme PstI ||  align="right" |1 ||  align="right" |1 ||  align="right" |1
+|H2O||  align="right" |8,8 ||  align="right" |5,6
 |-
-|H2O||  align="right" | 6,3 ||  align="right" | 2,8 ||  align="right" | 5,4
+|'''Total volume'''||  align="right" | 20||  align="right" |20
+|}
+<br />
+Preparation of gel:<br />
+,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 115 Volt, running time: 45 minutes
+<br />
+Expected sizes of constructs:
+*pSB1C3_leftITR_CMV:  2800 bp
+*pSB1C3_betaglobin_mVenus: 1200 bp, 2000 bp
+The corresponding bands were cut out and Gel-Extraction was performed according to protocol.
+<br />
+concentrations measured via NanoDrop:
+*pSB1C3_leftITR_CMV: 55,5 ng/µl
+*pSB1C3_betaglobin_mVenus:: 10,4 ng/µl
+<br />
+====<p style="font-size:15px; background-color:#66bbff;"><b>Continuation of Cloning of Rep40/52</b></p>====
+'''Investigator: Anna
+*Digestion of PCR products and vector:
+<br />
+{| border="1"
+| '''components'''   || align="right" |'''PCR product /µl''' || align="right" |'''vector /µl'''
 |-
-|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 20||  align="right" |20 ||  align="right" |20
+| DNA  ||  align="right" |19 ||  align="right" |10
+|-
+| BSA (10x) ||  align="right" |3 ||  align="right" | 3
+|-
+| Buffer 4 (10x)||  align="right" |3 ||  align="right" |3
+|-
+|Enzyme '''XbaI ||  align="right" |1 ||  align="right" |1
+|-
+|Enzyme '''SpeI ||  align="right" |1 ||  align="right" |1
+|-
+|H2O||  align="right" |3 ||  align="right" |12
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 30||  align="right" |30
 |}
+<br />
+<p style="font-size:13px; color:#68bbff;">'''''Comments''''': This time digestion was done with XbaI and SpeI (means it has to be checked if the inserts are cloned into the vector in the right orientation). </p> <br>
+*Purification of Rep40 and Rep52:
+For the purification 95 µl of buffer PBI was used.
+c(Rep40)= 12,5 ng/µl <br />
+c(Rep52)= 51,8  ng/µl <br />
 <br />
-,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 130 Volt, running time:45
+*Gelextraction of pSB1C3_RFC25_CFP:
+,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 120 Volt, running time:55 <br />
+µl loading dye (6x) for the sample, Marker: GeneRuler ladder mix (Fermentas)
 <br />
-<br>
-'''Results''': <br>
-[[File:Freiburg10 pSB1C3 lITR pTERT and pSB1C3 lITR CMV with GMK Insert.jpg|550px]] <br>
 <br />
+<br />
+<br />
+[[file:Digestion of pSB1C3_2.jpg]]
+<br />
+c(pSB1C3)= 10,59 ng/µl <br />
+c(pSB1C3_2)= 4,25 ng/µl
-*c(Insert)= 15,37 ng/µl; size: 627 bp <br />
-*c(Vector)= 50,84 ng/µl; size: 2869 bp
-*c(Vector)= 75,64 ng/µl; size: 2672 bp
 <br />
 *Ligation of PCR products and vector:
-For the Ligation 1µl T4 buffer (10x) and 1µl T4 ligase were used. Incubation time: 45 min
+For the Ligation 1µl T4 buffer (2x) and 1µl T4 ligase were used.
 <br />
 {| border="1"
-| ''' '''   || align="right" |'''pSB1C3_leftITR_CMV + GMK /µl'''|| align="right" |''' pSB1C3_leftITR_pTERT + GMK'''
+| ''' '''   || align="right" |'''Sample-no.'''|| align="right" |'''vector /µl''' || align="right" |'''insert /µl'''
 |-
-| Vector || align="right" |5,48 ||  align="right" | 6,21
+| pSB1C3 + Rep40 ||  align="right" |1 || align="right" |3,65 ||  align="right" |4,35
 |-
-| Insert || align="right" |2,52 ||  align="right" | 1,79
+| pSB1C3 + Rep52 ||  align="right" |2 ||  align="right" |5,87 ||  align="right" |2,13
 |-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 8||  align="right" | ||  align="right" |
 |}
 <br />
@@ Line 856: / Line 3,431: @@
 *Transformation:
-The transformation was done following the standard protocol using XL1 blue cells.<br />
+The transformation was done following the standard protocol using B21 cells.
-<br />
-====<p style="font-size:15px; background-color:#66bbff;"><b>Sequence analysis of pCerulean_VP1up</b></p>====
+====<p style="font-size:15px; background-color:#66bbff;"><b>PCR of bla_14FM  and ligation into pSB1C3_SDM_SspI and pSB1C3_SDM_PvuII for virobrick-production T</b></p>====
-<b>Investigator: Bea<br /></b>
+<br/>
-<p style="font-size:13px; color:#66bbff;">The assembled pCerulean_VP1up which serves as the first construct in the VP1 insertion cloning assembly was sent for sequencing. </p>
+Investigator: Anissa,Kerstin<br />
-<ul>
-<li>Plasmid used: P365</li>
-<li>Primer used: CMV-F</li>
-<li>Tube name: SB1</li>
-<li>Folder (Geneious): N-terminal Targeting --> pCerulean_VP1up_NLS</li>
-</ul>
 <br />
-<gallery widths=900px heights=300px>
-Image:Freiburg 10 SeqAnalysis of pCerulean VP1up NLS 03.09.2010.jpg
-</gallery>
 <br />
+<p style="font-size:13px; color:#68bbff;">'''''Comments''''': Because it still is unclear if SDM of pSB1C3_SspI_PvuII has worked, we decided to use the one time mutagenisised vector pSB1C3_SDM_SspI, to clone bla into it and to make the second mutation of PvuII after bla is inserted.  . </p> <br>
+<br>
+*'''PCR:
+(was performed following the standard protocol)
+<br>
+{| border="1"
+| '''Ingredients''' || align="right" |'''v(pTB106_bla14FM) - DMSO / µl''' || align="right" |'''v(pTB106_bla14FM) + DMSO / µl'''
+|-
+| 5X Phusion HF buffer ||  align="right" |10 ||  align="right" |10
+|-
+| 10 mM dNTP mix||  align="right" |1 ||  align="right" |1
+|-
+| forward primer: O116(P extreme f)||  align="right" |2,5 ||  align="right" |2,5
+|-
+| reverse primer: O117 (P extreme r) ||  align="right" |2,5 ||  align="right" |2,5
+|-
+| DNA Template 1ng ||  align="right" |5,3 µl ||  align="right" |5,3 µl
+|-
+| DMSO (1%)||  align="right" | 0,5 ||  align="right" | 0,5
+|-
+| Phusion Polymerase||  align="right" |0,5 ||  align="right" |0,5
+|-
+|H<sub>2</sub>O||  align="right" |28,2 ||  align="right" |27,7
+|-
+|Total volume||  align="right" |50 ||  align="right" |50
+|}
+<br>
-====<p style="font-size:15px; background-color:#66bbff;"><b>pCerulean_VP1up_NLS_Targeting molecule</b></p>====
+*''' PCR program:
-<b>Investigator: Bea<br /></b>
-<p style="font-size:13px; color:#66bbff;">Comment: For preparing the next step in the VP1 insertion, different targeting molecules will be fused to the construct pCerulean_VP1up_NLS. </p>
-<ol>
+{| border="1"
-<li>The first construct is the Affibody Z<sub>EGF-R:1907</sub> which was already cloned into the standard iGEM plasmid and can be sued for target tumor cells overexpressing the EGF receptor.</li>
+|'''PCR Program'''|| align="right" |'''temperature/ °C''' |'''time'''
-<li>The second construct is the mVenus (Yellow fluorescent protein) which can be used for imaging experiments</li>
+|-
-<li>Another motif will be the His-tag. Since the His-tag is very small, the oligos will be hybridized and directly ligated into the pCerulean backbone.</li>
+|1||  align="right" |98  ||  align="right" | 1'
-</ol>
+|-
-<br />
+|2||  align="right" |98 ||  align="right" | 15''
-<b>Digestion of vector:</b>
+|-
-<ul>
+|8x||  align="right" |61  ||  align="right" | 25''
-<li>Plasmid used: pCerulean_VP1up_NLS (P365) c=470 ng/µL</li>
+|-
-<li>Add BSA</li>
+|3 ||  align="right" |72 ||  align="right" | 15''
-<li>AgeI-HF and SpeI-HF were used</li>
+|-
+|4 ||  align="right" |98 ||  align="right" | 15''
+|-
+|5||  align="right" |72 ||  align="right" | 15''
+|-
+|1x||  align="right" |72 ||  align="right" | 5'
+|-
+|Hold||  align="right" |4
+|}
+<br>
+[[File:Freiburg10 pcr bla14FM.JPG|300px]]
+*'''Digestion PCR product:
+* DNA-Concentration: 4,2 ng/µl
+{| border="1"
+|'''components'''|| align="right" |'''volume / µl'''
+|-
+| DNA ||  align="right" | 28,5
+|-
+| BSA 100x ||  align="right" | 0,4
+|-
+|Buffer: 4 10x ||  align="right" | 4
+|-
+| Enzyme 1 (XbaI) ||  align="right" | 1
+|-
+| Enzyme 2 (PstI) ||  align="right" | 1
+|-
+| H<sub>2</sub>O ||  align="right" | 5,1
+|-
+| Total volume ||  align="right" | 40
+|-
+|}
+* ''' Purification of PCR product: (QlAquick Gel Extraction Kit)
+preparation of purification was made according to the standardprotocol
+<p style="font-size:13px; color:#FF0033;">'''''Comments''''': The wrong enzymes were used. Experiment has to be done tomorrow.</p> <br>
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Test digestion pSB1C3_CFP_SDM SspI and PvuII </b></p>====
+'''Investigator: Stefan'''<br>
+*buffer used: 2; Restriction-enzymes used: Enzyme 1: ClaI ; Enzyme 2: BpmI ; Enzyme 3: SspI ; Enzyme 4: PvuII
+<ul><li>Plasmids:</li>
+<ul><li>pSB1C3_SDM_SspI/PvuII '''P185''' (first tree lanes, cut with different enzymes)</li>
+<li>pSB1C3_RFC25_longlinker '''P105'''</li>
+<li>pSB1C3_CFP '''P51.1'''</li>
 </ul>
-<br/>
+</ul>
-<b>Protocol of the digestion of the vector:</b>
+<br />
 {| border="1"
-| align="left" | '''Components''' ||align="left"| <b>v<sub>pCerulean_VP1up_NLS</sub></b>/µL
+| align="left" | '''Components'''  ||align="left"| '''P185/µL''' ||align="left"| '''P185/µL''' ||align="left"| '''P185/µL''' ||align="left"| '''P105/µL''' ||align="left"| '''P51.1/µL'''
 |-
-| align="left" | DNA   ||align="left"| 3
+| align="left" | DNA  ||align="left"| 18||align="left"| 18||align="left"| 18||align="left"| 4,8||align="left"|6,8
 |-
-| align="left" | BSA (100x) ||align="left"| 2,5
+| align="left" | BSA (10x) ||align="left"| 2,5||align="left"| 2,5||align="left"| 2,5||align="left"| 2,5||align="left"| 2,5
 |-
-| align="left" | Buffer no. 4 (10x) ||align="left"| 2,5
+| align="left" | Buffer 2 (10x)  ||align="left"| -||align="left"| -||align="left"| -||align="left"| 2,5||align="left"| 2,5
 |-
-| align="left" | Enzyme 1 AgeI ||align="left"| 1
+| align="left" | Buffer 4 (10x)  ||align="left"| 2,5||align="left"| 2,5||align="left"| 2,5||align="left"| -||align="left"| -
 |-
-| align="left" | Enzyme 2 SpeI HF ||align="left"| 1
+| align="left" | Enzyme 1 ClaI (152)  ||align="left"| 0,5||align="left"| 0,5||align="left"| 0,5||align="left"| -||align="left"| -
 |-
-| align="left" | H<sub>2</sub>O ||align="left"| 15
+| align="left" | Enzyme 2 BpmI (144)  ||align="left"| 0,5||align="left"| 0,5||align="left"| 0,5||align="left"| -||align="left"| -
 |-
-| align="left" | '''Total volume''' ||align="left"| <b>25</b>
+| align="left" | Enzyme 3 SspI (68)  ||align="left"| -||align="left"| 0,5||align="left"| -||align="left"| 0,5||align="left"| 0,5
+|-
+| align="left" | Enzyme 4 PvuII (50) ||align="left"| -||align="left"| -||align="left"| 1||align="left"| 0,5||align="left"| 0,5
+|-
+| align="left" | H<sub>2</sub>O ||align="left"| 1||align="left"| -||align="left"| 0,5||align="left"| 14,2||align="left"| 12,2
+|-
+| align="left" | '''Total volume'''  ||align="left"| 25||align="left"| 25||align="left"| 25||align="left"| 25||align="left"| 25
 |}
 <br />
-<ul>
-<li>Incubation of the sample at 37°C</li>
+*Incubation: 75 minutes<br>
-<li>Incubation for 120 minutes</li>
+'''Agarosegel'''
-</ul>
 <br />
-The Targeting molecules were digested with different enzmyes than the vector for providing the ability to assemble the different constructs together without creating new restriction site but to delete them. This works by fusing NgoMIv and AgeI together.
+.5 g Agarose, 50 ml TAE, 3 µL GELRED, at 115 Volt, running time: 60 minutes
 <br />
 <br />
-<b>Digestion of the targeting molecules </b>
-<ul>
-<li>Plasmids used:</li>
+<br />
-<ol>
+[[File:Freiburg10 SspI PvuII ClaI BpmI later.png|500px|left|thumb|]]
-<li>pSB1C3_zEGF-R:1907 (P284) c=146 ng/µL</li>
+<br>
-<li>pGA14_mVenus(P60) c=280 ng/µL</li>
+<br>
-</ol>
+<br>
-<li>Add BSA</li>
+<br>
-<li>NgoMIV and SpeI-HF were used</li>
+<br>
-</ul>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+<br>
+comments: Test digestion of pSB1C3_SDM_SspI/PvuII with ClaI, BpmI and SspI looks the same as with ClaI and BpmI. Therefore we can assume that there is no additional restriction site within the vector. But still the bands above 3000 bp cannotz be explained. A new test digestion will be performed tomorrow to check the size of the vector.<br />
+The approach cut with ClaI, BpmI and PvuII looks strange. Propably, PvuII does not work correctly. New PvuII-HF was ordered and delivered so this can be verified tomorrow.<br />
+pSB1C3_RFC25_longlinker digested with SspI and PvuII seems to be not completely digested This could correspond to non-working PvuII.
+pSB1C3_CFP looks like expected.
+====<p style="font-size:15px; background-color:#66bbff;"><b>pSB1C3_SDM_Ssp1 (P125) sent for sequenzing</b></p>====
 <br/>
+Investigator: Stefan<br />
+comment: To verify the correct deletion of the SspI restriction site it was sent for sequenzing.
+Primer used: GATC_std_pTeSp-2
+====<p style="font-size:15px; background-color:#66bbff;"><b>Picking clones of pSB1C3_SDM_SspI/PvuII (P185)</b></p>====
+<br/>
+Investigator: Adrian<br />
+comment: pSB1C3_SDM_SspI/PvuII (P185) is empty. For plasmid production DYT + Cm was inoculated from the glycerol stock (B159).<br>
+=== 87. labday 12.08.2010===
+====<p style="font-size:15px; background-color:#FF0033;"><b>XL1blue are ready to use</b></p>====
+'''Investigator: Jessica'''
+<br>there are 60µl aliquots to use for one trafo
+====<p style="font-size:15px; background-color:#66bbff;"><b>Mini-Prep of pSB1C3_SDM_SspI/PvuII and pMA_RC_insert</b></p>====
+<br/>
+Investigator: Stefan<br />
+Gycerol stock was prepared for pMA_RC_insert and labeled B167. No glyerol stock for pSB1C3_SDM_SspI/PvuII because cells from earlier stock werer used for Mini-Prep.
+Miniprep was performed according to protocol.<br />
+Samples were labeled:<br />
+*pSB1C3_SDM_SspI/PvuII = P185.1
+*pMA_RC_insert = P190
+Concentrations:
+*pSB1C3_SDM_SspI/PvuII (P185.1): 257,2 ng/µl
+*pMA_RC_insert (P190): 339,5 ng/µl
+<br />
+No test digestion was performed.
+====<p style="font-size:15px; background-color:#66bbff;"><b>Biobrick Assembly: pSB1C3_lITR_CMV & pSB1C3_betaglobin_mVenus</b></p>====
+Investigator: <b>Chris L., Achim</B>
+<br />
+<p style="font-size:13px; color:#003399;"><b>Comments</b>: In order to proceed with the BioBrick assembly the plasmids pSB1C3_leftITR_CMV was cut with SpeI and PstI, pSB1C3_betaglobin_mVenus was cut with XbaI and PstI. The insert fragment containing betaglobin_mVenus was ligated to the vector fragment containing the leftITR_CMV promotor.</p>
+<br />
+<b>Ligation:</b> <br />
+For ligation, T4 ligase was used.
+<br />
+* 1µl T4-Ligase buffer (10x)
+* 8µl (Vector + Insert) mix
+* 1µl T4-Ligase
+Ligation was carried out as following:
+*pSB1C3_leftITR_CMV: 6,98 µl
+*pSB1C3_betaglobin_mVenus: 1,02 µl
+<br /> Incubation for 40 minutes.
+*Transformation:
+The transformation was done following the standard protocol using XL1B cells.
+<br />
+====<p style="font-size:15px; background-color:#66bbff;"><b>Repetition of cloning of bla14FM_viralbrick_MCS into pSB1C3_SDM_SspI</b></p>====
+<br/>
+Investigator: Anissa<br />
+<p style="font-size:13px; color:#003399;"><b>Comments</b>:Yesterday the pcr-product of bla14FM was cut with the wrong enzymes, so no overhangs could result. Today it will be repeated with the rihgt ones (SpeI and NgomIV) .</p>
+*'''Digestion of the PCR product bla14FM for 2 h :
+* DNA-Concentration: 10,2 ng/µl
 {| border="1"
-| align="left" | '''Components''' ||align="left"| <b>v<sub>ZEGFR (P284)</sub></b>/µL ||align="left"| <b>v<sub>pGA_mVenus (P60)</sub></b>/µL
+|'''components'''|| align="right" |'''volume / µl'''
 |-
-| align="left" | DNA   ||align="left"| 13 µl||align="left"| 7 µl
+| DNA ||  align="right" | 18
 |-
-| align="left" | BSA (10x) ||align="left"| 2,5 µl||align="left"| 2,5 µl
+| BSA 100x ||  align="right" | 3
 |-
-| align="left" | Buffer no. 4 (10x) ||align="left"| 2,5 µl||align="left"| 2,5 µl
+|Buffer: 4 10x ||  align="right" | 3
 |-
-| align="left" | Enzyme 1 NgoMIV- ||align="left"| 1,0 µl||align="left"| 1,0 µl
+| Enzyme 1 (NgomIV) ||  align="right" | 1
 |-
-| align="left" | Enzyme 2 AgeI HF ||align="left"| 1,0 µl||align="left"| 1,0 µl
+| Enzyme 2 (SpeI) ||  align="right" | 1
 |-
-| align="left" | H<sub>2</sub>O ||align="left"| 15 µl||align="left"| 15 µl
+| H<sub>2</sub>O ||  align="right" | 4
+|-
+| Total volume ||  align="right" | 30
 |-
-| align="left" | '''Total volume''' ||align="left"| <b>25</b> ||align="left"| <b>25</b>
 |}
-<ul>
-<li>Incubation of the sample at 37°C</li>
+* ''' Purification of PCR product: (QlAquick Gel Extraction Kit)
-<li>Incubation for 90 minutes</li>
-</ul>
+preparation of purification was made according to the standardprotocol
+<br/>
+*'''Digestion  of vector backbone pSB1C3_SDM_SspI for 2 h:
+<br/>
+*1 µg vector has been used
+{| border="1"
+|'''components'''|| align="right" |'''volume / µl'''
+|-
+| DNA ||  align="right" | 3,12
+|-
+| BSA 100x ||  align="right" | 1,5
+|-
+|Buffer: 4 10x ||  align="right" | 1,5
+|-
+| Enzyme 1 (NgomIV) ||  align="right" | 1
+|-
+| Enzyme 2 (SpeI) ||  align="right" | 1
+|-
+| H<sub>2</sub>O ||  align="right" | 6,88
+|-
+| Total volume ||  align="right" | 15
+|-
+|}
+<br/>
+*the cut vector was loaded on a preperative 1% agarose gel and the gel was running for 45 minutes
+[[File:Freiburg10 pSB1C3 SDM SspI cut.png|400px]]
+<br/>
+*gel was cut and gelextraction was performed according the qiagen standard protocol.
+<br/>
+*'''Ligation of pSB1C3_SDM_SspI and bla14FM:
+<br/>
+{| border="1"
+|'''components'''|| align="right" |'''volume / µl'''
+|-
+|t4 buffer (10X)  ||  align="right" | 1
+|-
+| t4 Ligase ||  align="right" | 1
+|-
+|vector DNA ||  align="right" | 2,72
+|-
+| Insert ||  align="right" | 5,28
+|-
+|}
+<br/>
+*'''Transformation: pSB1C3_SDM_SspI_bla14FM was transformed into BL21 following the stanard protocol
+====<p style="font-size:15px; background-color:#66bbff;"><b>Quickchange of the EaglII restriction site in the PMA_RepCap vector</b></p>====
+Investigator: <b>Chris L., Achim</B>
 <br />
-After incubation the samples were loaded on a 1% agarose gel. The obtained gel (after running the gel for 15 minutes) can be seen below.
+<p style="font-size:13px; color:#003399;"><b>Comments</b>: We performed a QuikChange mutagenesis on the synthesized PMA_RepCap vector (P190). The EaglII restriction enzyme also cuts NotI (IGEM standard) therefore EaglII has to be changed into a different recognition site. Primers were designed to change it into PvuII. The new QuikChange Lighting Site-Directed Mutagenesis Kit from Stratagene was used, therefore the mutagenesis was carried out as described in the QuikChange Manual. The PCR product was transformed into XL10-Gold cells, we used the IGEM standard protocol, except for the addition of ß-ME to the XL10-Gold cells.  : </p>
+PCR-reaction:
+{| border="1"
+| '''Volume / µl''' || align="right" |'''ingredients'''|| align="right" |'''recommended /µl'''
+|-
+| 2,5  ||  align="right" |10X reaction buffer ||  align="right" | 2,5
+|-
+| 2,9 ||  align="right" |P190 template (~10 ng)||  align="right" | 2,9 of 1:100 dilution
+|-
+| 0,51||  align="right" |forward primer: O122||  align="right" | 62,5 ng
+|-
+|0,51 ||  align="right" |reverse primer: O123 ||  align="right" | 62,5 ng
+|-
+|- ||  align="right" |DMSO ||  align="right" | -
+|-
+|0,5||  align="right" |dNTP||  align="right" | 250 µM each dNTP
+|-
+|17,6||  align="right" |H<sub>2</sub>O ||  align="right" |
+|-
+|0,5||  align="right" |QuikChange Lightning ennzyme(1.25) ||  align="right" |
+|}
+<br>
+PCR program:
+{| border="1"
+|'''Rounds'''|| align="right" |'''temperature/ °C'''|| align="right" |'''Time'''
+|-
+|1 ||  align="right" |95 ||  align="right" | 2 minutes
+|-
+|18 ||  align="right" |95||  align="right" |20 seconds
+|-
+|18 ||  align="right" |60 ||  align="right" | 10 seconds
+|-
+|18||  align="right" |68||  align="right" | 2 minutes (4 kb * 30 sec)
+|-
+|1||  align="right" |68||  align="right" | 5 minutes
+|}
+<br>
+The PCR product was digestet with Dpn I for 10 minutes at 37°C
+Plasmid was transformed into XL10-Gold cells.
+<br/>
+====<p style="font-size:15px; background-color:#ff00ff;"><b>Sequencing results of Rep68, Rep78 and AAP BioBricks</b></p>====
+Investigator: <b>Hanna</B>
 <br />
-<gallery widths=400px heights=400px>
+Comment: pSB1C3_Rep78 (P160), pSB1C3_Rep68 (P165) and pSB1C3_AAP (P170) were sent for sequencing twice. No sequencing made sense. Paradoxically the Rep78 sequencing result fit to the p5 promoter BioBrick... <br/>
-Image: Freiburg10 pCerulean VP1up NLS TargetingMolecule.jpg
+By having a closer look to the BioBrick PCR we found out that the fragment sizes didn't fit to the expected sequences. In addition to that the test digestion also showed some discrepancies. <br/>
-</gallery>
+Because we weren't able to find out in which steps of the BioBrick production things went wrong, we decided to discard all referring glycerol stocks and plasmids and to perform the Rep68, Rep78 and AAP BioBrick PCR again!!!
+<br/>
+<br/>
+====<p style="font-size:15px; background-color:#9acd32;"><b>Comment 13.08.2010 (Hanna):</b> We wondered how the whole Rep stuff could be sequenced reverse AND forward without any forward sequencing primer... By checking the "sequencing book" we found out that always the wrong primers were used: the GOI primers can be used in order to sequence the <b>G</b>ene <b>o</b>f <b>i</b>nterest = GOI (!) in pAAV_MCS and NOT the pSB1C3!!!!!!!!!</p>====
+<br/>
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Order oligos for CD-biobrick</b></p>====
+'''Investigator: Jessica and Kira'''
+<br>ordered on aug 12th<br>
+[[File:Freiburg10 oligos for CD-biobrick.jpg]]
+====<p style="font-size:15px; background-color:#66bbff;"><b>BioBrick assembly of pSB1C3_leftITR_CMV_mVenus</b></p>====
+Investigator: Stefan <br />
+comment: In order to assemble our complete constructs mVenus has to be included into the pSB1C3_leftITR_CMV vector. <br />
+<b>Digestion:</b> <br />
+{| border="1"
+| components:   || align="right" |pSB1C3_leftITR_CMV P188(Vector) || align="right" |pGA14_mVenus P60 (Insert)
+|-
+| DNA  ||  align="right" |6 ||  align="right" |8
+|-
+| BSA (10x) ||  align="right" |2 ||  align="right" | 2
+|-
+| Buffer 4 (10x)||  align="right" |2 ||  align="right" |2
+|-
+|Enzyme1 ||  align="right" |1 (SpeI) ||  align="right" |1 (Xba1)
+|-
+|Enzyme2 ||  align="right" |1 (PstI)||  align="right" |1 (PstI)
+|-
+|H2O||  align="right" |8 ||  align="right" |6
+|-
+|'''Total volume'''||  align="right" | 20||  align="right" |20
+|}
 <br />
-<b>Results: </b>The boxes mark fragments which ere cut out of the gel. The left lane (pCerulean) looks a bit strange, because Marker was added after the digestion reaction instead of Loading dye.
+Preparation of gel:<br />
+,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 110 Volt, running time: 45 minutes
 <br />
+[[File:Freiburg10 cloning of pSB1C3 leftITR CMV mVenus.png|500px]] <br />
+Expected sizes of constructs:
+*pSB1C3_leftITR_CMV:  2869 bp
+*pGA14_mVenus: 2896 bp, 756 bp
+The corresponding bands were cut out and Gel-Extraction was performed according to protocol.
 <br />
-<p style="font-size:13px; color:#33bbff;">Parallel, for assembling the His-Tag to the construct pCerulean_VP1up_NLS, oligos for the His-Tag in the RFC25 standard (provided by Gerrit) were hybridized and can directly be ligated in the digested vector. This strategy was used because of the smal size of the His-Tag which cannot be separated easily by the agarose gel. </p>
+concentrations measured via NanoDrop:
+*pSB1C3_leftITR_CMV: 39,2 ng/µl
+*pGA14_mVenus: 8,2 ng/µl
+<b>Ligation:</b> <br />
+T4 ligation was performed according to protocol. <br />
+Volumes used:
+*vector: 1,67 ng/µl
+*insert: 6,33 ng/µl
+<b>Transformation:</b> <br />
+bacterial strain used: XL1bB<br />
+antibiotic used for plate: chlorampenicol<br />
+Transformation was performed according to protocol.<br />
+Plate was prepared and put in 37°C room.
+====<p style="font-size:15px; background-color:#66bbff;"><b>Opened a BioBrick box</b></p>====
+<b>Investigator: Bea</b>
 <br />
-<b>Hybridization of the His-Oligos</b>
+In order to "save" the plasmids/BioBricks which has been prepared and confirmed for submitting it to the parts registry a new box have been prepared. The box should contain 30 µL of the desired construct cloned into the pSB1C3 vector and the BBa number given from the headquarter. <br />
+[[File:Freiburg10 BioBrick highlighting in Nomenclature list.JPG|400px|thumb]]
+The first BioBricks which are in this box are:
 <ul>
-<li>10µL oligo1 (1:10)</li>
+<li>pSB1C3_hGH (P136): Bba_K404002</li>
-<li>10µL oligo2 (1:10)</li>
+<li>pSB1C3_betaglobin (P133: Bba_K404001 </li>
-<li>4µL 100mM Tris-Cl pH 8 </li>
+<li>pSB1C3_CMV (P145): Bba_K404003</li>
-<li>10µL 5mM MgCl<sub>2</sub></li>
+<li>pSB1C3_leftITR (P175): Bba_K404006</li>
-<li>8µL H<sub>2</sub>O</li>
+<li>pSB1C3_rightITR (P172): Bba_K404005</li>
+<li>pSB1C3_mGMK (P156): Bba_K404004</li>
 </ul>
-The used programm for the hybridization:
+In our nomenclature plasmid excel list the constructs which we aliquoted should be highlighted in blue and commented with the given Bba number. Additionally it should be taken in consideration that enough DNA should be in the "working" plasmid box. Therefore, if necessary, inoculate DYT medium for Mini-Preps.<br />
+<br />
+In this case ALL the glycerol stocks were used  for incoluating 10 mL DYT medium containing 10 µL chloramphenicol respectively.
 <ul>
-<li>99°C 7´</li>
+<p style="color:#66bbff;">To do: Mini-Preps of the over night cultures.</p>
-<li>99°C 1´</li>
-<li>-1°C R=0,3°/s </li>
-<li>Goto 2 rep 74</li>
-<li>Hold 4°C</li>
 </ul>
 <br/>
-After the gel extraction of a T4 ligation was performed.
-<ul>
+=== 88. labday 13.08.2010===
-<p style="font-size:13px; color:#cc3300;">Affibody Z<sub>EGF-R:1907</sub>:</p>
+====<p style="font-size:15px; background-color:#66bbff;"><b>Continuation:pSB1C3_SDM_SspI_bla14FM</b></p>====
-v<sub>Cerulean_VP1up_NLS</sub> = 5,82µL<br />
+Investigator: Patrick <br>
-v<sub>ZEGF-R:1907</sub> = 2,18µL <br />
+Intention: receive enough plasmid for a sequencing and maybe futher working steps. <br>
-<br />
+Three clones were picked in the morning to inoculate DYT and perform a mini-prep in the evening and to send them for sequencing. The three clones were picked and prepped according to the standard protocol yielding the following DNA concentrations:
-<p style="font-size:13px; color:#cc3300;">mVenus Z:</p>
+*pSB1C3_SDM_SspI_bla14FM clone 1: 65,15 ng/µl , Sequencing labeled: PS3.1
-v<sub>Cerulean_VP1up_NLS</sub> = 4,04µL<br />
+*pSB1C3_SDM_SspI_bla14FM clone 2: 22,3 ng/µl , Sequencing labeled: PS3.2
-v<sub>mVenus</sub> = 3,96 µL<br />
+*pSB1C3_SDM_SspI_bla14FM clone 3: 62,3 ng/µl , Sequencing labeled: PS3.3
-<br />
+<br>
-<p style="font-size:13px; color:#cc3300;">6xHisTag:</p>
+Used primer: seq_pSB1C3_VR2_rev (O51) <br>
-v<sub>Cerulean_VP1up_NLS</sub> = 0,2µL<br />
+Results: see http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/index.php/Laborjournal#Sequence_analysis_of_pSB1C3_SDM_SspI_BLA
-v<sub>6xHisTag</sub> = 7,98µL <br />
-</ul>
+====<p style="font-size:15px; background-color:#66bbff;"><b>Mini-preps of pSB1C3_hgh,pSB1C3_beta globin,pSB1C3_left ITR,pSB1C3_right ITR,pSB1C3_mGMK,pSB1C3_CMV</b></p>====
-<br />
-<b>Next steps:</b> Picking clones of the trafo plates (containing Kanamycin) and perform the Mini-Prep. The obtaining constructs finally will be fused to the VP2/3 protein which results in the final construct for the VP1 targeting approach.
 <br/>
+<p style="font-size:13px; color:#003399;"><b>Comments</b>:new mini-preps of the glycerol-stocks ofpSB1C3_hgh(=B103),pSB1C3_beta globin(=B100),pSB1C3_left ITR (=B143),pSB1C3_right ITR (=B140),pSB1C3_mGMK (=B125),pSB1C3_CMV   : </p>
 <br/>
+{| border="1"
+|'''components'''|| align="right" |'''concentration in ng/µl'''
+|-
+| P191 (pSB1C3_right ITR)||  align="right" | 100,74
+|-
+|P192 (pSB1C3_beta-globin) ||  align="right" |240,08
+|-
+|P193 (pSB1C3_CMV) ||  align="right" | 333,89
+|-
+|P194 (pSB1C3_hgh) ||  align="right" |328,42
+|-
+| P195 (pSB1C3_mGMK) ||  align="right" |258,63
+|-
+| P196 (pSB1C3_left ITR) ||  align="right" |173,98
+|-
+|}
-====<p style="font-size:15px; background-color:#66bbff;"><b>3rd Repetition of Mini-Preps and test digestion for Loop insertion BioBricks</b></p>====
+====<p style="font-size:15px; background-color:#FF00ff;"><b>Design and ordering of oligos for VP fusion targeting approaches</b></p>====
+'''Investigator: Hanna'''
+<br/>
+<p> <b>Comment:</b> In order to target the EGFR receptor of our A431 cells different approaches have been figured out: Besides loop insertions, N-terminal fusion to the VP2 protein will be performed. In addition to that a VP1 insertion approach (after Grieger et al., 2007) was planned. <br/>
+Fusion and insertion molecules will be e.g. His-tag, Affibody, Darpin, GFP. These approaches can be combinated with the loop insertions. <br/>
+For this purpose the following oligos were ordered today: <br/></p>
+<br/>
+[[File:Freiburg10 N-terminalFusion1.jpg|450px|thumb|left|]]
+[[File:Freiburg10 N-terminalFusion2.jpg|450px|thumb|right|]]
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
+<br/>
-<b>Investigator: Achim, Anna<br /></b>
+====<p style="font-size:15px; background-color:#66bbff;"><b>Mini-Prep and Test digestion of Rep40 and Rep52 of the cloning experiment ("Cloning of Rep40/52" 11.08.2010 Investigator: Anna) </b></p>====
+Investigator: <b>Chris L., Achim</B>
+<br />
-Sequencing results of Loop insertion BioBricks from 02.09.10; the following clones looked well:
+<p style="font-size:13px; color:#003399;"><b>Comments</b>: There are small and big colonies on the plate. Maybe problems with the agar plate. Picked colonies of pSB1C3_Rep40 sample 1 and pSB1C3_Rep52 sample 1 are small colonies. Picked colonies of pSB1C3_Rep40 sample 2 + 3 and pSB1C3_Rep52 sample 2 + 3 are standard size colonies.</p>
+<br/>
-*pSB1C3_587_KO_RGD_clone6.4<br>
+'''Nanodrop'''
-*PSB1C3_587_KO_His_clone9.4
+* Rep 40 Sample 1: 156,26 ng/µl '''P197'''
+* Rep 40 Sample 2: 200,05 ng/µl '''P198'''
+* Rep 40 Sample 3: 144,06 ng/µl '''P199'''
+* Rep 52 Sample 1: 173,36 ng/µl '''P200'''
+* Rep 52 Sample 2: 160,75 ng/µl '''P201'''
+* Rep 52 Sample 3: 295,77 ng/µl '''P202'''
 <br>
-<p style="font-size:13px; color:#003399;"><b>Update</b>: 9 of the 14 ViralBricks looked well (sequencing results from 01. - 03.09.). Two new clones of the remaining constructs were prepared and test digested. </p>
-<b>Test digestion:</b>
 <br>
+'''Test digestion''' 800ng DNA
 {| border="1"
-| components ||Volume for each sample /µl
+| components   || align="right" |P145 /µl || align="right" |P146 /µl || align="right" |P145 /µl || align="right" |P146 /µl|| align="right" |P145 /µl || align="right" |P146 /µl
 |-
-| DNA  || 10
+| DNA  ||  align="right" | 5,1||  align="right" |4||  align="right" |5,6||  align="right" |4,6||  align="right" |5||  align="right" |2,7
 |-
-| BSA (10x) ||1,5
+| BSA (10x) ||  align="right" | 2||  align="right" |2||  align="right" |2||  align="right" |2||  align="right" |2||  align="right" |2
 |-
-| Buffer 4 (10x) ||1,5
+| Buffer 4 (10x)||  align="right" | 2||  align="right" |2||  align="right" |2||  align="right" |2||  align="right" |2||  align="right" |2
 |-
-|Enzyme EcoRI HF ||0,5
+| Enzyme 1: XbaI ||  align="right" | 0,5||  align="right" |0,5||  align="right" |0,5||  align="right" |0,5||  align="right" |0,5||  align="right" |0,5
 |-
-|Enzyme NotI HF ||0,5
+| Enzyme 2: SpeI ||  align="right" | 0,5||  align="right" |0,5||  align="right" |0,5||  align="right" |0,5||  align="right" |0,5||  align="right" |0,5
 |-
-|H2O || 1
+|H<sub>2</sub>O||  align="right" | 9,9||  align="right" |11||  align="right" |9,4||  align="right" |10,4||  align="right" |10||  align="right" |12,3
 |-
-|'''Total volume /µl'''||15
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | '''20'''||  align="right" | '''20'''||  align="right" | '''20'''||  align="right" | '''20'''||  align="right" | '''20'''||  align="right" | '''20'''
 |}
-<br />
+<br>
+Incubation time: 45 minutes, Incubation temperature: 37°
+<br>
+<br>
+<br>
+,5 g Agarose, 50ml x TAE, 3µl GELRED, at 115 Volt, running time: 45 minutes
+{| border="1" cellspacing="0" cellpadding="2" bordercolor="black"
+!Sample
+!Sample/µl]
+!Loading dye (6x)/µl
+!Expected size 1 (Geneious)
+!Expected size 2 (Geneious)
+|--
+|Rep 40 1
+|20 µl
+| 4 µl
+|____ bp
+| 940 bp
+|--
+|Rep 40 2
+|20 µl
+| 4 µl
+|____ bp
+| 940 bp
+|--
+|Rep 40 3
+|20 µl
+| 4 µl
+|____ bp
+| 940 bp
+|--
+|Rep 52 1
+|20 µl
+| 4 µl
+|____ bp
+|1198 bp
+|--
+|Rep 52 2
+|20 µl
+| 4 µl
+|____ bp
+|1198 bp
+|--
+|Rep 52 3
+|20 µl
+| 4 µl
+|____ bp
+|1198 bp
+|--
+|}
+{| align=right
+|}
 {| border="1"
+|
+!Marker
+!Sample Rep40 1 /20µl
+!Sample Rep40 2 /20µl
+!Sample Rep40 3 /20µl
+!Sample Rep52 1 /20µl
+!Sample Rep52 2 /20µl
+!Sample Rep52 3 /20µl
+|-
+!Lane
+| 1
+| 2
+| 3
+| 4
+| 5
+| 6
+| 7
+|-
+|}
-|align="left" | '''Components''' ||align="left"| '''453 BAP''' ||align="left"| '''453 Z34C'''||align="left"| '''587 Z34C'''||align="left"| '''587 KO Z34C'''||align="left"| '''587 KO Z34C SPACER'''
+agarose gel: 1%, digestion: 45 minutes, 37°C
+<p style="font-size:13px; color:#68bbff;">'''''Comments:'''''Results look bad. Rep52 clone 3 looks good, send for sequencing. </p><br>
+ '''</p>
+====<p style="font-size:15px; background-color:#66bbff;"><b>Repetition of Rep 40 and Rep 52 ligation and transformation with the vector pSB1C3_CFP</b></p>====
+Investigator: <b>Chris L.</B>
+<br />
+*Ligation of PCR products and vector:
+For the Ligation 1µl T4 buffer (10x) and 1µl T4 ligase were used.
+<br />
+{| border="1"
+| ''' '''   || align="right" |'''Sample-no.'''|| align="right" |'''vector /µl''' || align="right" |'''insert /µl'''
 |-
-| align="left" | Clone||align="left"|1.5 + 1.6 ||align="left"|11.5 + 11.6 ||align="left"|12.5 + 12.6  ||align="left"|13.5 + 13.6||align="left"| 14.5 + 14.6
+| pSB1C3 + Rep40 ||  align="right" |1 || align="right" |4,92 ||  align="right" |3,08
 |-
+| pSB1C3 + Rep52 ||  align="right" |2 ||  align="right" |6,47 ||  align="right" |1,53
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | ||  align="right" | 10 ||  align="right" | 10
 |}
+<br />
+*Transformation:
+The transformation was done following the standard protocol using XL1B cells.
 <br/>
-Incubation time: 1 h, Incubation temperature: 37°
 <br/>
-<b>Preparation of gel:</b><br/>
+====<p style="font-size:15px; background-color:#ff00ff;"><b>Strategy for VP2 N-terminal fusion and VP1 insertion of targeting moelcules</b></p>====
-g Agarose, 100 ml TAE (1%), 6 µl GELRED , at 115 Volt, running time: 45 minutes
+Investigator: <b>Hanna</B>
 <br />
+<p><b>Comment:</b> In order to target the EGFR receptor of tumor cells via Affibody or Darpin (antibody fragment is also possible!!!), or in order to expose e.g. His-Tags on the virus surface, two approaches have been figured out. <br/>
 <br/>
-[[File:3.9.10 AA.png|400px]]
+[[File:Freiburg10_N-terminalFusion_Strategy.JPG]]
-<br />
 <br/>
-<b>Expected fragment sizes /bp:</b> <br/>
+[[File:Freiburg10_N-terminalFusion_Strategy2.JPG]]
-pSB1C3: 2051 bp<br/>
+[[File:Freiburg10 N-terminalFusion Strategy3.JPG]]
-BAP: ~150<br/>
-Z34C: ~ 200<br/>
 <br/>
-<p style="font-size:13px; color:#003399;"><b>Comment</b>: The following clones were sent for sequencing: 1.6, 12.6 ,13.6 and 14.5.<br/> To do: Retrafo of clone6.4 and clone9.4 and preparation of glycerol stocks. </p>
-====<p style="font-size:15px; background-color:#66bbff;"><b>Cloning of Cap into pAAV_RC_ins-rep: preparation for SDM</b></p>====
+===='''pSB1C3_Rep52 (P202) sent for sequencing'''====
-<b>Investigator: Stefan </b>
-<p style="font-size:13px; color:red;"><b>Comment</b>: Cloning Cap into pAAV still does not work as planned. As another approach Cap can be cut using BsiWI and XcmI and performing a SDM in the part of Cap not cloned into pAAV. Primers are ordered and should arrive on monday to proceed.</p>
+'''Investigator: Chris L.'''<br>
-<br/>
-'''Digestion:'''
+Primer used: Reverse Primer VR2
+====<p style="font-size:15px; background-color:#66bbff;">'''Repetition: Biobrick production of Rep 68, 78 and AAP'''</p>====
+'''Investigator: Stefan'''<br>
+Aim of the experiment:
+We want to produce biobricks from Rep 68, Rep 78 and the AAP.
+*Plasmids used as template:
+Rep_68_ex (p119):   c = 470,6 ng/µl <br>
+Rep_78_(p122):      c = 566,8 ng/µl <br>
+pAAV-RC containing AAP ORF (p50):    c = 378,5 ng/µl <br>
+*Primer used:
+For Rep_68_ex: Praefix_68_78_ex & Suffix_40_68_ex<br>
+For Rep_78_ex: Praefix_68_78_ex & Suffix_52_78_ex<br>
+For AAP_ex: Praefix_AAP_ex & Suffix_AAP_ex
+<br>
+*'''PCR:
+(was performed following the standard protocol)
+<br>
 {| border="1"
-| components   || align="right" |pMA_RepCap Vector_SDM_InsPvuII (P211) || align="right" |pAAV_RC_ins-rep (P250)
+| '''Ingredients''' || align="right" |'''Volume / µl''' || align="right" |'''Rep68'''|| align="right" |'''Rep78''' || align="right" |'''AAP'''
+|-
+| 5X Phusion HF buffer ||  align="right" |10 ||  align="right" | ||  align="right" | ||  align="right" |
+|-
+| 10 mM dNTP mix||  align="right" |1||  align="right" |  ||  align="right" | ||  align="right" |
+|-
+| forward primer: ||  align="right" |2,5||  align="right" | ||  align="right" | ||  align="right" |
 |-
-| DNA  ||  align="right" |7,9 ||  align="right" | 2,1
+| reverse primer: ||  align="right" |2,5||  align="right" | ||  align="right" | ||  align="right" |
 |-
-| Buffer 2 (10x)||  align="right" |2 ||  align="right" | 2
+| DNA Template||  align="right" |***||  align="right" |2,5 µl ||  align="right" |2 µl||  align="right" |3 µl
 |-
-|XcmI ||  align="right" |1 ||  align="right" |1
+| DMSO (2%)||  align="right" | ||  align="right" | - ||  align="right" | - ||  align="right" | 1 µl
 |-
-|BsiWI  ||  align="right" |1||  align="right" |1
+| Phusion Polymerase||  align="right" |0,5||  align="right" | ||  align="right" | ||  align="right" |
 |-
-|H<sub>2</sub>O||  align="right" |8,1 ||  align="right" | 13,9
+|H<sub>2</sub>O||  align="right" |*** ||  align="right" | 31 µl||  align="right" | 31,5 µl||  align="right" |29,5 µl
 |-
-|'''Total volume '''||  align="right" |20||  align="right" | 20
+|Total volume||  align="right" |50
 |}
+<br>
+PCR program:
+{| border="1"
+|'''PCR Program'''|| align="right" |'''temperature/ °C'''|| align="right" |'''Time''' || align="right" |'''Rep68'''|| align="right" |'''Rep78'''|| align="right" |'''AAP'''
+|-
+|1||  align="right" |98 ||  align="right" |1min||  align="right" | ||  align="right" | ||  align="right" |
+|-
+|2||  align="right" |98 ||  align="right" |15s||   align="right" | ||  align="right" | ||  align="right" |
+|-
+|3||  align="right" |*** ||  align="right" |25s||  align="right" |63°C||  align="right" |62°C||  align="right" |64°C
+|-
+|4 (step 2-4 8x) ||  align="right" |72||  align="right" |***||  align="right" |24s ||  align="right" |27s ||  align="right" | 10s
+|-
+|5 ||  align="right" |98||  align="right" | 15s||  align="right" | ||  align="right" | ||  align="right" |
+|-
+|6||  align="right" |***||  align="right" |25s|| align="right" |68°C||  align="right" |64°C||  align="right" |68°C
+|-
+|7||  align="right" |72||  align="right" |***||  align="right" |24s||  align="right" |27s||  align="right" |10s
+|-
+|8 (step 6-8 17x)||  align="right" |72||  align="right" |5min||  align="right" | ||  align="right" | ||  align="right" |
+|-
+|Hold||  align="right" |4||  align="right" |  ||  align="right" | ||  align="right" | ||  align="right" |
+|}
+<br>
+Used agarose gel:
+,5 g Agarose,50 ml TBE (1%), 3 µl GELRED , at 115 Volt, running time:45 minutes
+[[File:Freiburg10 68 78 AAP.jpg|500px|]]
+<p style="font-size:15px; font-weight: bold; color: blue;">Gel extraction</p>
 <br />
-<p style="font-size:13px; color:red;"><b>Comment</b>:Digestion was performed using two steps, first incubating for 1 hour at 37 °C, afterwards for 1,5 hours at 55 °C.</p><br />
+Gel extraction was perfomed according to protocol.
-<br />
-'''Gel:''' <br />
+*Digestion of PCR products and vector:
-,5 g Agarose,50 ml TAE (1%), 5 µl EtBr , at 115 Volt, running time: 50 minutes
 <br />
+{| border="1"
+| '''components'''   || align="right" |'''PCR products /µl''' || align="right" |'''vector /µl'''
+|-
+| DNA  ||  align="right" |29 ||  align="right" |11
+|-
+| BSA (10x) ||  align="right" |4 ||  align="right" | 2
+|-
+| Buffer 4 (10x)||  align="right" |4 ||  align="right" |2
+|-
+|Enzyme '''XbaI ||  align="right" |1 ||  align="right" |1
+|-
+|Enzyme '''SpeI ||  align="right" |1 ||  align="right" |1
+|-
+|H2O||  align="right" |1 ||  align="right" |3
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 40||  align="right" |20
+|}
 <br />
+<p style="font-size:13px; color:#68bbff;">'''''Comments''''': Digestion was done with XbaI and SpeI, it has to be checked if the inserts are cloned into the vector in the right orientation. </p> <br>
+*Purification of Rep68, 78 and AAP:
+For the purification 200 µl of buffer PBI was used.
+c(Rep68)= 14,3 ng/µl <br />
+c(Rep78)= 12,0 ng/µl <br />
+c(AAP)= 25,1 ng/µl
 <br />
-<br />
-[[File:Freiburg10 pCerulean pMA pAAV.png|500px|]]
+*Gelextraction of pSB1C3_RFC25_CFP:
+,5 g Agarose,50 ml TBE (1%), 3 µl GELRED , at 115 Volt, running time:50 minutes <br />
+µl loading dye (6x) for the sample, Marker: GeneRuler ladder mix (Fermentas)
 <br />
 <br />
 <br />
 <br />
+[[File:Freiburg10 pSB1C3 CFP 130810.jpg|500px|]]
 <br />
-'''Gelextraction:'''<br />
-The gelextraction was performed according to the standard protocol. DNA concentration of the extracts:
+c(pSB1C3)= 6,9 ng/µl <br />
-* pMA_RepCap Vector_SDM_InsPvuII (P211): c= 6,26 ng/µl
-* pAAV_RC_ins-rep (P250): c= 13,72 ng/µl
-<br>
-'''Quick Ligation:'''<br />
-<p style="font-size:13px; color:red;"><b>Comment</b>: XcmI produces only 1 base overhang, therefore Quickligase was used for ligation and incubation time increased.</p>
-The  Ligation was performed as following:<br />
-* Vector Volume: 4,59 µl
-* Insert Volume: 4,41 µl
-<br>
+<br />
-* 10 µl QuickLigase buffer (2x)
-* 9 µl (Vector + Insert) mix
-* 1 µl QuickLigase
-<br> Incubating for 60 minutes.
-<br>
+*T4 ligation of PCR products and vector:
-'''Transformation:'''<br />
-Trafo was performed according to the standard protocol (XL1b). The cells were plated on a agar plate with ampicilin.
+For the Ligation 1µl buffer (10x) and 1µl T4 ligase were used.
-<br>
+<br />
+{| border="1"
+| ''' '''   || align="right" |'''vector /µl''' || align="right" |'''insert /µl'''
+|-
+| pSB1C3 + Rep68 || align="right" |3,78 ||  align="right" |4,24
+|-
+| pSB1C32 + Rep78 ||  align="right" |3,13 ||  align="right" |4,87
+|-
+| pSB1C3 + AAP ||  align="right" |6,42 ||  align="right" |1,58
+|-
-===110. labday 04.09.2010===
+|}
-====<p style="font-size:15px; background-color:#66bbff;"><b>Continuation: Cloning CFP_middlelinker (from pSB1C3_CFP_middlelinker, P276) into pCerulean (P273): Sequencing results of P381 and P385</b></p>====
+<br />
-Investigator:Patrick
+*Transformation:
-Sequencing results of P381 & P385 Labelling: P381-CMV_rev & P385-CMV_rev:
+The transformation was done following the standard protocol using XL1b cells.
-A wrong primer was used so there are no relevant sequence data yet.
-On sunday i will sent these clones again for sequencing. Primer: GATC_std_CMV-F
-[[Image:Freiburg10_Kopfkratzen.gif|thumb|400px|Ha ich war schneller als Bea beim "Kopfkratzen-setzen" *lol*]]
+=== 89. labday 14.08.2010===
+====<p style="font-size:15px; background-color:#66bbff;"><b>Sequence analysis of pSB1C3_SDM_SspI_BLA</b></p>====
+Investigator: <b>Patrick, Bea </b>
+<br />
+<p style="font-size:13px; color:#003399;"><b>Comments</b>: Sequence analysis of three clones revealed that all sequences contain some mutations in the regions where the primer annealed. This was due to the extreme primer lentgh. Primers that long should be ordered as HPLC purified in order to avoid mutations in the primer sequence.</p>
+<ol>
+<li>Clone 1: Mutation in the SalI site of the loop insertion site in the Viral Brick MCS lead to the removal of the recognition site. CANNOT be used for the loop insertions!!!!</li>
+<li>Clone 2:  Mutation in the region of the primer upstream of the loop insertion sites SalI and PvuII.</li>
+<li>Clone 3: Mutation in the region of the primer downstream of the loop insertion sites SalI and PvuII.</li>
+</ol>
+<br />
+<gallery widths=450px heights=300px perrow=2 caption="Sequencing results of pSB1C3_SDM of SspI_BLA clone 2 and pSB1C3_SDM of SspI_BLA clone 3">
+Image:Freiburg10 Sequence analysis of pSB1C3 SDM SspI BLA clone2.jpg|Clone 2
+Image:Freiburg10 Sequence analysis of pSB1C3 SDM SspI BLA clone3.jpg|Clone 3
+</gallery>
+<br />
+<p style="font-size:13px; color:#33cc66;"><b>Next steps: </b> Two additional clones will be picked and sent for sequencing (clones 4 and 5). In order to obtain a construct without any mutations, clone 2 and clone 3 couldbe cloned together. Each clone will be digested with SalI and BamHI. Clone 2 will be the "insert", clone 3 is going to be the "vector". Therefore the fragments will (hopefully) not contain anymore mutations in the relevant sequence. </p>
-'''Hiermit verspreche ich dass es noch jede Menge Kopfkratzer, Laboraufsichtswichtel und pinke Panter geben wird (Patrick)'''
+====<p style="font-size:15px; background-color:#66bbff;"><b>Mini Preps of PMA_RepCap vector and pSB1C3_left ITR_CMV_betaglobin_mVenus</b></p>====
+<br/>
+'''Investigator: Chris L., Bea'''
+<br>
+<p style="font-size:13px; color:#003399;"><b>Comments</b>:new mini-preps of the glycerol-stocks of pSB1C3_leftITR_CMV_betaglobin_mVenus clone 1 (=B179), pSB1C3_leftITR_CMV_betaglobin_mVenus clone 2 (=B180), pSB1C3_leftITR_CMV_betaglobin_mVenus clone 3 (=B181), pMA_RepCap Vector_SDM_InsPvuII clone 1, (=B182), pMA_RepCap Vector_SDM_InsPvuII clone 2 (=B183) and pMA_RepCap Vector_SDM_InsPvuII clone 3 (=B184)</p>
+<br/>
+<b>Comment: The plamsid numbers in the picture (P179-P184) correspond to the glycerol stocks B179-B184. The corresponding plasmid numbers are: P208-P213. </b>
+<br />
+'''Nanodrop'''
+* pSB1C3_leftITR_CMV_betaglobin_mVenus clone 1: 256,64 ng/µl '''B179'''
+* pSB1C3_leftITR_CMV_betaglobin_mVenus clone 2: 274,86 ng/µl '''B180'''
+* pSB1C3_leftITR_CMV_betaglobin_mVenus clone 3: 217,20 ng/µl '''B181'''
+* pMA_RepCap Vector_SDM_InsPvuII clone 1: 253,71 ng/µl '''B182'''
+* pMA_RepCap Vector_SDM_InsPvuII clone 2: 195,64 ng/µl '''B183'''
+* pMA_RepCap Vector_SDM_InsPvuII clone 3: 144,61 ng/µl '''B184'''
-<br><br><br><br>
+<br>
-<br><br><br><br>
+<br>
+'''Test digestion''' 800ng DNA
+{| border="1"
+| components   || align="right" |B179 /µl || align="right" |B180 /µl || align="right" |B181 /µl || align="right" |B182 /µl|| align="right" |B183 /µl || align="right" |B184 /µl|| align="right" |pMA_RepCap Vector /µl
+|-
+| DNA  ||  align="right" | 3,1||  align="right" |2,9||  align="right" |3,7||  align="right" |3,1||  align="right" |4||  align="right" |5,5||  align="right" | 2,4
+|-
+| BSA (10x) ||  align="right" | 2||  align="right" |2||  align="right" |2||  align="right" |2||  align="right" |2||  align="right" |2||  align="right" |2
+|-
+| Buffer 4 (10x)||  align="right" | 2||  align="right" |2||  align="right" |2||  align="right" |2||  align="right" |2||  align="right" |2||  align="right" |2
+|-
+| Enzyme 1: NgoMIV ||  align="right" | 0,5||  align="right" |0,5||  align="right" |0,5||  align="right" |0||  align="right" |0||  align="right" |0 ||  align="right" |0
+|-
+| Enzyme 2: EcoRI ||  align="right" | 0,5||  align="right" |0,5||  align="right" |0,5||  align="right" |0||  align="right" |0||  align="right" |0||  align="right" |0
+|-
+| Enzyme 2: PvuII ||  align="right" | 0||  align="right" |0||  align="right" |0 ||  align="right" |0,5||  align="right" |0,5||  align="right" |0,5||  align="right" |0,5
+|-
+|H<sub>2</sub>O||  align="right" | 11,9||  align="right" |12,1||  align="right" |11,3||  align="right" |12,4||  align="right" |11,5||  align="right" |10||  align="right" | 13,1
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | '''20'''||  align="right" | '''20'''||  align="right" | '''20'''||  align="right" | '''20'''||  align="right" | '''20'''||  align="right" | '''20'''||  align="right" | '''20'''
+|}
+<br>
+Incubation time: 45 minutes, Incubation temperature: 37°
+<br>
+<br>
+<br>
+,5 g Agarose, 50ml x TAE, 3µl GELRED, at 115 Volt, running time: 45 minutes
-====<p style="font-size:15px; background-color:#66bbff;"><b>Harvest viral particles, Transduction</b></p>====
+<br />
+<b>Results of test digestion</b>
-<b> Investigator:Kerstin, Adrian </b>
+[[File:Freiburg10 Test digestion of pSB1C3 Bba fourparts SDM pMA RC insert 14 08.jpg|500px]]
+<br />
+<br />
+<br />
+<b>Results</b>: Two (three) different approaches can be seen on the agarose gel.
+<ol>
+<li style="font-size:13px; color:#66bbff;">P178-P181 (blue): The plasmid pSB1C3_leftITR_CMV_betaglobin_mVenus was digested with NgoMIV and EcoRI. Expected bands were: <b> 2873bp and 1343 </b>. As it can be seen in the picture, the two fragments ran too high (~300bp). As it is almost normal for the pSB1C3 plasmid, we should figure out why this is always the problem for this vector.</li>
+<li style="font-size:13px; color:#cc3333;">P182-P183 (red): The plasmid pMA_RepCap_SDM_insPvuII was digested with PvuII as well as the control vetor pMA_RepCap where no site-directed mutagenesis was performed in order to see the difference. As it can be seen in the picture above, the expected band sizes of <b>263bp,1384bp and 2133bp</b> correspond to the bands detected in the gel. The control vector instead reveals only two bands detectable. Therefore site-directed mutagenesis was successfully performed.</li>
+<li style="font-size:13px; color:#33cc33;">P177 (green): pSB1C3_hTERT. For further details see extra part below (Test digestion of pSB1C3_hTERT.</li>
+</ol>
-*Harvest viral paricles from one plate of transfection from 01.09.2010 (10 plates, same treatment (10µg of each plasmid P357, P263, P356))
+====<p style="font-size:15px; background-color:#66bbff;"><b>Mini-Prep of pSB1C3_leftITR_CMV_mVenus</b></p>====
-*Transduction:
+<b>Investigator: Stefan</b><br>
-#  1x 6-well: 0,5ml of virus from 01.09.2010 (testing R/C P326)
+Glycerol stocks were prepared:
-#  1x 6-well: 0,5ml of virus from 01.09.2010 (testing R/C P325)
+<li>B177 = pSB1C3_leftITR_CMV_mVenus clone 1
-#  4x 6-well: 10x 0,5ml and 4x 1ml of virus from 01.09.2010 (stratagene R/C)
+<li>B178 = pSB1C3_leftITR_CMV_mVenus clone 2
-#  4x 6-well: 10x 0,5ml and 4x 1ml of virus from 04.09.2010 (10 plates same treatment)
-#  6x 6-well: 0,5ml of virus from 21.08.2010 (TKGMK; 18x pH 7,10 and 6x pH 7,12)
-====<p style="font-size:15px; background-color:#66bbff;"><b>Repetition of Hybridisation and Cloning for Loop insertion BioBricks</b></p>====
-<b>Investigator: Achim, Anna<br /></b>
+Mini-Prep following the standard protokol
+<br />
+<li>P206 = pSB1C3_leftITR_CMV_mVenus clone 1 = 277,9 ng/µl
+<li>P207 = pSB1C3_leftITR_CMV_mVenus clone 2 = 260,3 ng/µl
-*Samples:
+<br />
-: 453_BAP
 <br>
-: 453_Z34C<br>
-: 587_Z34C<br>
-: 587_KO_Z34C<br>
-: 587_KO_Z34C_Spacer<br>
 <br>
-<p style="font-size:13px; color:#003399;"><b>Comment</b>: New approaches of the Hybridisation and Fill-in reactions were done because it didn't work the first time. A possible reason is that the klenow enzyme wasn't inactivated. In addition, the conditions for ligation will be improved. Also the ligation of 453_BAP was done again.</p>
+<b>Test digestion:</b>
+or test digestion, pSB1C3_leftITR_CMV (P188) was digested as well. <br />
-<b>Digestion:</b>
-<br>
 {| border="1"
-| components ||Volume Vector 587  ||Volume Vector 453 || Sample 11  || Sample 12 || Sample 13 || Sample 14
+| '''Ingredients''' || align="right" |'''clone 1/µl'''|| align="right" |'''clone 2/µl''' || align="right" |'''P188/µl'''
 |-
-| DNA  || 3,7 || 3,7|| 6 || 6 || 6 || 6
+| DNA: ||  align="right" |3,5 ||  align="right" |3,5 ||  align="right" |4
 |-
-| BSA (10x) ||-|| -|| -|| -|| -|| -
+| BSA (10x): ||  align="right" |2  ||  align="right" |2 ||  align="right" |2
 |-
-| Buffer 4 (10x) ||2|| 2 || 2|| 2|| 2|| 2
+| Buffer 4: ||  align="right" |2 ||  align="right" |2 ||  align="right" |2
 |-
-|Enzyme 1° ||Bam || Ssp || Ssp || Bam || Bam || Bam
+| Enzyme 1 EcoRI: ||  align="right" |0,5 ||  align="right" |0,5 ||  align="right" |0,5
 |-
-|Enzyme 2° ||Pvu|| Sal|| Sal || Pvu || Pvu || Pvu
+| Enzyme 2 AgeI||  align="right" |0,5 ||  align="right" |0,5||  align="right" |0,5
 |-
-|H2O || 12,3 || 12,3 || 10 || 10 || 10 || 10
+|H<sub>2</sub>O||  align="right" | 6,5||  align="right" | 6,5||  align="right" |6
 |-
-|'''Total volume /µl'''||20
 |}
 <br />
+<ul>
+All samples were loaded on a 1% agarose gel:
+<li>GeneRuler Ladder Mix (7µl)</li>
+<li>P206 = pSB1C3_leftITR_CMV_mVenus clone 1 </li>
+<li>P207 = pSB1C3_leftITR_CMV_mVenus clone 2 </li>
+<li>P188 = pSB1C3_leftITR_CMV</li>
-° 1 µl each
+</ul>
+<br />
+[[File:Freiburg10 test digestion leftITR CMV mVenus 140810.jpg|300px]]
+<br />
+<br />
+<br />
+comment: Through digestion, fragments would have similar sizes. Therefore, a new digestion will be performed tomorrow.
-<b>Preparation of gel:</b><br/>
+====<p style="font-size:15px; background-color:#66bbff;"><b>Test digestion of pSB1C3_pHTERT</b></p>====
-g Agarose, 100 ml TAE (1%), 6 µl GELRED , at 115 Volt, running time: 50 minutes
+Investigator: <b>Bea </b>
+<br />
+<p style="font-size:13px; color:#003399;"><b>Comments</b>: pSB1C3_hTERT was sent for sequencing and revealed that the PCR and the inserting of the PCR product : promoter for hTERT was sucessfully performed. But the sequencing results showed a new AgeI restriciton site in the plasmid backbone. We could not see if the new recognition site was due to the bad sequence read or that there is really a new AgeI site. Therefore, a test digestion will be perfomed with PstI and AgeI in order to figure our wheter AgeI is present in the backbone or not.</p>
+<br />
+<p style="font-size:13px;"><b>Sequence analysis of pSB1C3_hTERT: </b></p>
+<gallery widths=450px heights=300px perrow=2 caption="Sequencing results of pSB1C3_hTERT">
+Image:Freiburg10 Sequence analysis of pSB1C3 hTERT suffix.jpg
+Image:Freiburg10 Sequence analysis of pSB1C3 hTERT CAT mutations.jpg
+</gallery>
+<br />
+<br />
+<b>First the sequenced plasmid P177 was digested:</b>
+<br />
+<table border=1 cellpadding=1 cellspacing=1 width=284 style='border-collapse:
+ collapse;table-layout:fixed;width:214pt'>
+ <tr height=30 style='mso-height-source:userset;height:22.5pt'>
+  <td height=30 class=xl6312733 width=142 style='height:22.5pt;width:107pt'>&nbsp;</td>
+  <td class=xl6412733 width=142 style='border-left:none;width:107pt'>P177/µL</td>
+ </tr>
+ <tr height=30 style='mso-height-source:userset;height:22.5pt'>
-====<p style="font-size:15px; background-color:#66bbff;"><b>Repetition: Prepatation for SDM: cloning of Cap into pAAV</b></p>====
+  <td height=30 class=xl6512733 width=142 style='height:22.5pt;border-top:none;
-Investigator: Stefan
+  width:107pt'>DNA</td>
+  <td class=xl6612733 style='border-top:none;border-left:none'>3</td>
+ </tr>
+ <tr height=30 style='mso-height-source:userset;height:22.5pt'>
+  <td height=30 class=xl6512733 width=142 style='height:22.5pt;border-top:none;
+  width:107pt'>BSA (10x)</td>
+  <td class=xl6612733 style='border-top:none;border-left:none'>1,5</td>
+ </tr>
-[[Image:Freiburg10_Kopfkratzen.gif|thumb|right|Schönen Abend dir noch]]
+ <tr height=30 style='mso-height-source:userset;height:22.5pt'>
+  <td height=30 class=xl6512733 width=142 style='height:22.5pt;border-top:none;
+  width:107pt'>Buffer 4<span style='mso-spacerun:yes'>   </span>(10x)</td>
+  <td class=xl6612733 style='border-top:none;border-left:none'>1,5</td>
+ </tr>
+ <tr height=30 style='mso-height-source:userset;height:22.5pt'>
+  <td height=30 class=xl6512733 width=142 style='height:22.5pt;border-top:none;
+  width:107pt'>Enzyme PstI</td>
-<p style="font-size:13px; color:red;"><b>Comment</b>: On yesterday's plates nothing grew. Because gelex and ligation products were stored in coldroom, new ligation and trafo approaches were performed. </p>
+  <td class=xl6612733 style='border-top:none;border-left:none'>0,5</td>
-<br/>
+ </tr>
+ <tr height=30 style='mso-height-source:userset;height:22.5pt'>
+  <td height=30 class=xl6512733 width=142 style='height:22.5pt;border-top:none;
+  width:107pt'>Enzyme AgeI</td>
+  <td class=xl6612733 style='border-top:none;border-left:none'>0,5</td>
+ </tr>
+ <tr height=30 style='mso-height-source:userset;height:22.5pt'>
+  <td height=30 class=xl6512733 width=142 style='height:22.5pt;border-top:none;
+  width:107pt'>H2O</td>
+  <td>8</td>
+ </tr>
+ <tr height=30;height:22.5pt'>
+  <td height=30  width=142 style='height:22.5pt;
+  width:107pt'><b>Total volume</b></td>
+  <td><b>15</b></td>
+ </tr>
+ <tr height=0 style='display:none'>
+  <td width=142 style='width:107pt'></td>
+  <td width=142 style='width:107pt'></td>
+ </tr>
+</table>
 <br />
-'''Ligation approaches:'''<br />
+<ul>
-* ligation with Quick Ligase (as performed yesterday)
+<li>Incubation time: 45minutes</li>
-* ligation with T4 Ligase
+<li>Incubation tempereature: 37°C</li>
+</ul>
+After the incubation,the samples were loaded on the 1% agarose gel, and run at 110 V for 45 minutes.
 <br />
 <br />
-'''Transformation approaches:'''<br />
+<b>Result of the test digestion:</b>
-* Quick Ligase (approach from yesterday):
-** 2 µl of ligation product
-** 4 µl of ligation product<br />
 <br />
-* Quick Ligase (new approach):
+<gallery widths=400px heights=300px caption="Test digestion of pSB1C3_hTERT">
-** 2 µl of ligation product
+Image: Freiburg10 Testdigestion pSB1C3 hTERT 14 08.jpg
-** 4 µl of ligation product<br />
+</gallery>
 <br />
-* T4 Ligase:
+<p style="font-size:13px; color:#33cc33;"><b>Results:</b> As it can be seen in the sequencing results of pSB1C3_hTERT there could have been an additional AgeI site in the vector. If AgeI would have been in the vector, two fragments have been expected by digetsing the plasmid with AgeI and PstI. As it can be seen in the agarose gel, lane 11 (labeled with the green P177) only reveals one lane instead of two. Therefore it can be assumed that NO AgeI site is in the pSB1C3 backbone.</p>
-** 2 µl of ligation product
-** 4 µl of ligation product<br />
+====<p style="font-size:15px; background-color:#66bbff;"><b>Picking clones ... </b></p>====
+Investigator: Patrick
+Clones were picked saturday night so that a mini-prep could be performed on sunday.
+=== 90. labday 15.08.2010===
+====<p style="font-size:15px; background-color:#66bbff;"><b>Sequence analysis of pSB1C3_Rep52</b></p>====
+<b>Investigator: Bea </b>
 <br />
-'''Transformation:'''<br />
+<p style="font-size:13px; color:#003399;"><b>Comments</b>: Clone 3 was sent for sequencing because this clone revealed the right band sizes of the test digestion performed friday. For more details see: [http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/index.php/Laborjournal#Mini-Prep_and_Test_digestion_of_Rep40_and_Rep52_of_the_cloning_experiment_.28.22Cloning_of_Rep40.2F52.22_11.08.2010_Investigator:_Anna.29 Test digestion] </p>
-Trafo of each approach was performed according to the standard protocol (XL1b). The cells were plated on a agar plate with ampicilin.
+<gallery widths=700px heights=300px caption="Sequencing results of pSB1C3_Rep52 clone 3">
-<br>
+Image:Freiburg10 Sequence analysis of pSB1C3 Rep52 14 08 2010.JPG
+</gallery>
+<br />
+<b>Results:</b> <p style="color:#00bbff;"> Sequence assembly showed that the suffix of the Rep protein 52 is ok and that PCR worked well. </p> <p style="color:#990000;">There can be seen that a silent mutation from AGG to AGA was inserted, but it will have no effect on the protein because codon usage in <i>H. sapiens </i>is nearly the same for both codons.</p>
+The prefix could not be analysed because of bad sequence read quality. For further verification, another sequencing with the forward primer has to be performed.
+<br />
+<b>Next steps: Send plasmid for another sequencing round with forward primer in order to analyse the prefix. </b>
+<br />
+<br />
+[http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/index.php/Laborjournal top of page]<br />
-====<p style="font-size:15px; background-color:#66bbff;"><b>Ligation and trafo of the modified Cap insert , the Viral Bricks 1, 11, 12, 13 and 14</b></p>====
+====<p style="font-size:15px; background-color:#66bbff;"><b>Mini-Prep of pSB1C3_Rep68, pSB1C3_Rep78, pSB1C3_RepAAP, pSB1C3_Rep40, pSB1C3_Rep52</b></p>====
+<b>Investigator: Stefan</b><br>
+<ul>
+<b>Glycerol stocks were prepared:</b>
+<li>B185 = pSB1C3_Rep68 clone 1
+<li>B186 = pSB1C3_Rep68 clone 2
+<li>B187 = pSB1C3_Rep68 clone 3<br />
+<br />
-<b>Investigator: Volker<br /></b>
+<li>B188 = pSB1C3_Rep78 clone 1
+<li>B189 = pSB1C3_Rep78 clone 2
+<li>B190 = pSB1C3_Rep78 clone 3<br />
+<br />
+<li>B191 = pSB1C3_AAP clone 1
+<li>B192 = pSB1C3_AAP clone 2
+<li>B193 = pSB1C3_AAP clone 3<br />
+<br />
-<p style="font-size:15px; font-weight: bold; color: blue;">Ligation</p>
+<li>B194 = pSB1C3_Rep40 clone 1
+<li>B195 = pSB1C3_Rep40 clone 2<br />
 <br />
-{| border="1"
-|'''Construct'''
+<li>B196 = pSB1C3_Rep52 clone 1
-|'''Vector (µl)'''
+<li>B197 = pSB1C3_Rep52 clone 2<br />
-|'''Insert(µl)'''
+<br />
+<li>B198 = pSB1C3_SDM_SspI_Bla14FM clone 4
+<li>B199 = pSB1C3_SDM_SspI_Bla14FM clone 5<br />
+<br />
+<br />
+<br />
+<b>Mini-Prep following the standard protokol</b>
+<br />
+<li>P208 = pSB1C3_Rep68 clone 1 c=230,0
+<li>P209 = pSB1C3_Rep68 clone 2 c=160,5
+<li>P210 = pSB1C3_Rep68 clone 3 c=128,6 <br />
+<br />
+<li>P211 = pSB1C3_Rep78 clone 1 c=150,8
+<li>P212 = pSB1C3_Rep78 clone 2 c=108,6
+<li>P213 = pSB1C3_Rep78 clone 3 c=131,3<br />
+<br />
+<li>P214 = pSB1C3_AAP clone 1 c=142,1
+<li>P215 = pSB1C3_AAP clone 2 c=148,3
+<li>P216 = pSB1C3_AAP clone 3 c=163,0<br />
+<br />
+<li>P217 = pSB1C3_Rep40 clone 1 c=164,5
+<li>P218 = pSB1C3_Rep40 clone 2 c=<145,1br />
+<br />
+<li>P219 = pSB1C3_Rep52 clone 1 c=156,0
+<li>P220 = pSB1C3_Rep52 clone 2 c=164,0<br />
+<br />
+<li>P221 = pSB1C3_SDM_SspI_Bla14FM clone 4 c=220,4
+<li>P222 = pSB1C3_SDM_SspI_Bla14FM clone 5 c=252,2<br />
+</ul>
+<br />
+<br />
+<br />
+<b>Test digestion:</b> <br />
+No test digestion for pSB1C3_SDM_SspI_Bla14FM clone 4 and 5.<br />
+For test digestion, pSB1C3_leftITR_CMV_mVenus (P206-207) and pSB1C3_leftITR_CMV (P188) was digested as well. <br />
+Samples P208-220 were digested with XbaI and SpeI.<br />
+Samples P207, P207 and P188 were digested with XbaI and NgoMIV.<br />
+Gel used:<br />
+ml TAE (1x), 1 g agarose, 6 µl GELRED<br />
+V, 50 minutes
+{| border="1"
+| '''Ingredients''' || '''P208/µl'''|| |'''P209/µl''' || |'''P210/µl'''|| '''P211/µl'''|| |'''P212/µl''' || '''P213/µl'''|| |'''P214/µl''' || '''P215/µl'''|| |'''P216/µl''' || '''P217/µl'''|| |'''P218/µl''' || '''P219/µl'''|| |'''P220/µl''' || '''P206/µl'''|| |'''P207/µl''' || |'''P188/µl'''
 |-
-|'''ViralBrick 1 in 453'''
+| DNA: ||  |4||  |6 ||  |7  ||  |6 ||  |9 || |7 ||  |6 ||  |6 ||  |6||  |6 ||  |6  ||  |6 ||  |6 || |3,5 ||  |3,5 ||  |4
-| 7.91
-| 0.09
 |-
-|'''ViralBrick 11 in 453'''
+| BSA (10x): ||  |2  ||  |2 ||  |2||  |2  ||  |2 ||  |2||  |2  ||  |2 ||  |2||  |2  ||  |2 ||  |2||  |2  ||  |2 ||  |2||  |2
-| 6.17
-| 1.83
 |-
-|'''ViralBrick 12 in 587'''
+| Buffer 4: ||  |2  ||  |2 ||  |2||  |2  ||  |2 ||  |2||  |2  ||  |2 ||  |2||  |2  ||  |2 ||  |2||  |2  ||  |2 ||  |2||  |2
-| 6.15
-| 1.85
 |-
-|'''ViralBrick 13 in 587'''
+| Enzyme 1 ||  |0,5 || |0,5 ||  |0,5||  |0,5 || |0,5 ||  |0,5||  |0,5 || |0,5 ||  |0,5||  |0,5 || |0,5 ||  |0,5||  |0,5 || |0,5 ||  |0,5||  |0,5
-| 5.3
-| 2.7
 |-
-|'''ViralBrick 14 in 587'''
+| Enzyme 2 ||  |0,5 || |0,5 ||  |0,5||  |0,5 || |0,5 ||  |0,5||  |0,5 || |0,5 ||  |0,5||  |0,5 || |0,5 ||  |0,5||  |0,5 || |0,5 ||  |0,5||  |0,5
-| 4.46
-| 3.54
 |-
-|'''p211 in pAAV-RC'''
+|H<sub>2</sub>O||  | 11||  | 9||  |8||  | 9||  | 6||  |8||  | 9||  | 9||  |9||  | 9||  | 9||  |9||  | 9||  | 11,5||  |11,5||  | 11
-| 5.52
-| 3.54
-|-
-|'''p211 in pAAV-RC'''
-| 5.52
-| 3.54
 |-
 |}
-<br />
-====<p style="font-size:15px; background-color:#66bbff;"><b>Preparation of PBS Buffer</b></p>====
-Investigator: Volker
-Two liters of PBS buffer were prepared for the column purification of the viral particles. The following protocol was used:
-*dissolve the following in 800ml ddH<sub>2</sub>O:
-**8g of NaCl
-**0.2g of KCl
-**1.44g of Na<sub>2</sub>HP0<sub>$</sub> (1.69 because of the crystal water in the reagent)
-**0.24 g of KH<sub>2</sub>PO<sub>4</sub>
-*adjust to pH 7.4
-*adjust to 1000ml
-*steril filtrate the solution
-===111. labday 05.09.2010===
-====<p style="font-size:15px; background-color:#66bbff;"><b>Mini-prep of glycerol stock pMA_RepCap Vector_SDM_InsPvuII clone 1 (B182)</b></p>====
-<b>Investigator: Stefan<br /></b>
 <br />
-Glycerol stock: Because glycerol stock B182 was not mixed before putting into -80 °C freezer the cells died. Therefore a new glycerol stock was prepared and labled B302.
-Mini-Prep was performed according to the standard protocol. Two preps were prepared:
 <br />
-<li>P363 = pMA_RepCap Vector_SDM_InsPvuII clone 1 (1) = 215,6 ng/µl
+[[File:Freiburg10 Rep40-78 mVenus.jpg|700px]]
-<li>P364 = pMA_RepCap Vector_SDM_InsPvuII clone 1 (2) = 230,5 ng/µl
 <br />
-====<p style="font-size:15px; background-color:#ff00ff;"><b>Picking clones of pCerulean_Zegfr:1907_"Linker" and pCerulean_CFP_MiddleLinker</b></p>====
-<b>Investigator: Hanna<br /></b>
-<br/>
-clones of each construct (1. pCerulean_Zegfr:1907_ShortLinker, 2. pCerulean_Zegfr:1907_MiddleLinker, 3. pCerulean_Zegfr:1907_LongLinker, 4. pCerulean_Zegfr:1907_SEG and 5. pCerulean_CFP_MiddleLinker) were picked.
-<br/>
-<br/>
-<b>To do tomorrow (6.9.):</b> Mini-Preps and Test digestion (with EcoRI and PstI).
-===112. labday 06.09.2010===
-====<p style="font-size:15px; background-color:#66bbff;"><b>Production of Ampicilin and Chloramphenicol</b></p>====
-<b>Investigator: Jessica<br /></b>
 <br />
-* 10ml ethanol (70%) containing 1g Amp in 60µl aliquots
+<br />
-* 10ml ethanol (70%) containing 0,25g Cm in 60 µl aliquots
+comment: Rep- and AAP approaches have to be repeated. We did not realize that the vector can religate! Plasmids and glycerol stocks were thrown away.
+====<p style="font-size:15px; background-color:#66bbff;"><b>Inoculation of CD colony</b></p>====
+Investigator: Kira
+One colony was picked from agar plate and dispersed into 10 ml DYT+ Amp and incubated over night @ 37 C.
 <html>
 </div>
 </html>

Team:Freiburg Bioware/testpage

From 2010.igem.org

Revision as of 11:34, 6 September 2010

Contents

76.Labortag 01.08.2010

Picking clones of pSB1C3_CMV

77.Labortag 02.08.2010

Sequenzing of pSB1C3_RFC25_longlinker, pSB1C3_RFC25_SEG, pSB1C3_RFC25_GSAT

Sequencing of pGA14_Prefix-leftITR

Repetition of test digestion pSB1C3_CFP SDM SspI and PvuII

Mini-Prep and Test digestion of pSB1C3_CMV

Sent for sequencing

Preparation of competent E.coli

Last Mini-Prep and test digestion of ITRs

BioBrick production: mGMK in pSB1C3

Sequencing results of SDM Rep 68 & 78

78.Labortag 03.08.2010

Results of sequencing pSB1C3_CFP_SDM_PvuII

Repetition of the quickchange site-directed mutagenesis of pAAV_RC_1.1_SalI

PCR for Biobrickproduction of Rep 40, 52, 68, 78 and APP

Continuation of preparation of competent E.coli

Sequencing of pSB1C3

Design of Primer for p5 Promoter WT and TATA-less BioBrick production

79.Labortag 04.08.2010

Cloning of right ITR and left ITR into pSB1C3_RFC25_CFP

Cloning of SDM SspI and SDM PvuII

2nd Repetition of Quickchange site-directed mutagenesis of pAAV_RC_1.1_SalI

Mini-Prep of pSB1C3_mGMK

cell culture

Repetition of cloning of SDM SspI and SDM PvuII

Test transformation of XL1 competent cells

Sequencing results of ITRs

Cloning of Rep68, Rep78 and AAP into pSB1C3

80.Labortag 05.08.2010

New LB Agar was prepared.

Sequenc analysis of BioBricks: CMV, hGH and beta globin

Cellculture

Picking clones of pSB1C3_AAP_2, pSB1C3_AAP, pSB1C3_Rep78_2, pSB1C3_Rep78, pSB1C3_Rep68_2 and pSB1C3_Rep68

PCR and ligation for biobrick-production of pSB1C3_hTERT

Transformation evaluation of XL1B cells and repetition of transformation

Cloning of SDM SspI and SDM PvuII

Miniprep of p158 and p159

81.Labortag 06.08.2010

Cloning Rep40 & Rep52 into pSB1C3

BioBrick Assembly of pSB1C3_beta globin_mVenus

Test digestion of SalI SDM

ITR test digestion of pAAV_MCS

Miniprep of pSBC13_Rep78, pSB1C3_Rep68, pSB1C3_AAP, pSB1C3_rightITR and psB1C3_leftITR

82.Labortag 07.08.2010

Cellculture

Continuation: Cloning Rep40 & Rep52 into pSB1C3

Mini-Prep and test digestion of pSB1C3_SDM_SspI/PvuII

Evaluation of test transformation with XL1 blue cells and pUCI

Biobrick production of p5 promoter from pTAV2 and pAAV_RC

Sequencing results of SalI SDM

83. Labortag 08.08.2010

84. Labortag 09.08.2010

Midi-Prep Inoculation

Continuation: Cloning Rep40 & Rep52 into pSB1C3

Repetition: BioBrick production of Rep40 & Rep52

Sequence analysis of pSB1C3_mGMK

Mini-Prep of pSB1C3_hTERT, pSB1C3_beta-globin_mVenus, pSB1C3_pTAV2(P5), pSB1C3_pAAV_RC(P5TATAles)

Cell culture

Transfection on HEK293

Transduction of HT1080

Passaging and seeding of A431

BioBrick Assembly of pSB1C3_leftITR_CMV and pSB1C3_hGH_rightITR

Repetition: Cloning of SDM SspI and SDM PvuII

Design and ordering of primer for P40 Promoter BioBrick production

85. labday 10.08.2010

Retrafo with RepCap gene (Mr.Gene)

Continuation: Cloning Rep40 & Rep52 into pSB1C3

Midi-Prep of pAAV_RC, pAAV_RC_1.2 SDM SalI (P158), pAAV_RFC25_mGMK_TK30 clone 1 (P81) and 2 (P82)

Results of sequencing pSB1C3_pTAV2(P5) and Psb1C3_pAAV_RC(P5TATAless)

Repetition: BioBrick production of Rep40 and Rep 52

Preparation of competent XL1blue and testtrafo

Repetition: Mini-Prep and test digestion of pSB1C3_SDM_SspI/PvuII

Picking clones of pSB1C3_SDM_SspI/PvuII

86. labday 11.08.2010

Biobrick Assembly:Picking Clones, Miniprep, Testdigestion of CMV&lITR/ hGH & rITR