Team:Freiburg Bioware/NoteBook/Labjournal/September2

From 2010.igem.org

(Difference between revisions)

Latest revision as of 21:35, 27 October 2010

=> Back to Notebook overview

NoteBook Navigator

September

124. labday 19.09.2010

Continuation with Colony-PCR of pSB1C3_CD and ViralBrick motif Z34C

Investigator: Bea

Comment: Since the colony PCR of the last try did not work exactly the way we expected it, another colony PCR approach with new primers was conducted.

Loading plan:
upper lanes

M   CD1  CD2  CD3  CD4  CD5  CD6  CD7  CD8  CD9  CD10   +ctrl(CFP) +ctrl(BAP) -ctrl(pAAV_MCS)   11Q1  12Q1  13Q1 13Q2  M

lower lanes

M   11T41  11T42  11T43  11T44    12T41  12T42  12T43  12T44    13T41  13T42  13T43  13T44    14T41  14T42 14T43  14T44  M

Expected sizes of the PCR products are:

Cytosine deaminase (CD) = 1300bp
Z34C loops insertion motif = 220bp
Positive control 1 = CFP = 750bp
Positive control 2 = BAP_587 = 170bp

Results:
The Colony PCR of the Cytosine Deaminase (CD) did not work out. The detectable bands at around 700 bp correspond to CFP. Therefore, BioBrick production of the CD must be repeated. The following three bands represent the controls. Three different controls were used. The first corresponds to pSB1C3_CFP, the second to BAP_587 and third control is the negative control. Unfortunately now bands can be detected in the postive controls. A faint band can be seen in the negative control which is the only lane in which no band should be detectable.
The following bands after the three controls correspond to the approaches of the Z34C Viralbrick production. Some bands in the lower and the upper lanes show positive results. The corresponding inoculated overnight culture were centrifuged and prepared in order to perform a Mini-Prep tomorrow.

Freiburg10 ColonyPCR Results 19.09.2010.jpg

Comment: hmm, seems that the CD-assambly didn't work at all.. Should i try it again or are we gonna skip it for good due to other priorities?(kira)
No, we cannot skip it. Can we change something else?? Any ideas what we can alter in the protocol? Because problem is that we are still waiting for the tk... so we should aswell focus on the other prodrug activating enzmye!! (Bea)

Testtransduction of the final modified capsid coding constructs

Investigator: Adrian

Aim of the experiment:
During the project 22 silent nucleotide exchange mutations were introduced into the capsid coding construct to make it compatible with the RFC standards and to have single cutting restriction enzymes flanking the 453 and the 587 loop sequence. Two point mutations had to be dismissed, because either a first test transduction showed that the construct was not working anymore or the insertion of the synthesized gene posed serious problems, because the restriction enzyme did not work.
Finally, we have a construct that is shown to produce infectious particles comparable to the current AAV systems and carries 20 point mutations. Now we can announce that the Adeno-associated Virus is compatible to the RFC standard and the idea to replace the loop sequences via ViralBricks works!

Impression from the moment:

The construct with the insertion of the Rep and the Cap synthesis worked! Reintroduction of the KpnI restriction site recovered the functionality of the viral genome!

Miniprep of serveral constructs

Investigator: Stefan

Glycerol stocks were prepared:

B430 = pCerulean_ZEGFR:1907_Longlinker_VP2/3
B431 = pCerulean_CFP_Middlelinker_VP2/3_insCap
B432 = pCerulean_ZEGFR:1907_Shortlinker_VP2/3_insCap

Mini-Prep was performed according to the standard protocol

P527 = pCerulean_ZEGFR:1907_Longlinker_VP2/3 c = 230,61 ng/µl
P528 = pCerulean_CFP_Middlelinker_VP2/3_insCap c = 290,81 ng/µl
P529 = pCerulean_ZEGFR:1907_Shortlinker_VP2/3_insCap c = 269,39 ng/µl

Several other constructs were preped, but need to be confirmed before being added to plasmid/glycerol stock.

125. labday 20.09.2010

Picking the clones and preparing the over-night culture

Investigator: Kira

VP2/3_Gsat-linker as well as VP2/3_cap_Gsat-linker plates contain colonies, thus 3 clones from each plate were inoculated into 5 ml DYT+ 5ul Chloramphenicol and incubated @ 37 C

Minipreps and Sequencing of ViralBrick clones

Investigator: Achim

The following clones were prepped:

Quickligation:
- 11.1, c = 85,41 ng/µl
- 13.1, c = 96,93 ng/µl
T4-Ligation:
- 11.4, c = 76,42 ng/µl
- 12.1, c = 80,36 ng/µl
- 12.4, c = 85,43 ng/µl
- 13.1, c = 90,06 ng/µl
- 13.2, c = 80,87 ng/µl
- 13.4, c = 76,62 ng/µl
- 14.1, c = 76,50 ng/µl
- 14.2, c = 98,52 ng/µl

Clones 11.4, 12.1, 13.2, 14.2 (T4) were sent for sequencing.

Cloning of pCerulean_Affibody_VP2/3 and pSB1C3_Affibody_middlelinker_GFP_his

Investigator: Jessica

Comment:Affibody_VP2/3 will be cloned in pCerulean and Affibody_middlelinker will be cloned together with GFP_His in pSB1C3

P407= pCerulean_CFP_middlelinker c=482,76 ng/µl
P516= pSB1C3_ZEGFR:1907_VP2/3 clone 1 c= 191,6 ng/µl
P290= pSB1C3_Affibody_Middlelinker clone 1 c= 227,4 ng/µl
P518= pSB1C3_GFP_RFC25_upper band clone 1 c= 138,3 ng/µl
P520= pSB1C3_GFP_RFC25_lower band clone 1 c= 141,6 ng/µl

Digestion:

components	P407	P516	P290	P518	P520
DNA	3,5	10	7	10	10
BSA (10x)	2	2	2	2	2
Buffer 4 (10x)	2	2	2	2	2
EcoRI	0,8	0,8	-	-	-
AgeI	0,8	0,8	0,8	-	-
NgoMIV	-	-	-	0,8	0,8
SpeI	-	-	0,8	0,8	0,8
H₂O	10,9	4,4	7,4	4,4	4,4
Total volume	20	20	20	20	20

1,0 g Agarose,100 ml TAE (1%), 6 µl GELRED , at 120 Volt

P516, P518, P520 will be repeated tomorrow (no DNA after gel-ex)

Gelextraction:

The gelextraction was performed according to the standard protocol. DNA concentration of the extracts:

P407 c= 6,5 ng/µl
P516 c= - ng/µl
P290 c= 7,3 ng/µl
P518 c= - ng/µl
P520 c= - ng/µl

stands in 4°C room for comtinuation tomorrow

Cloning of P5_TATAless downstream of pSB1C3_001_RC_insrepcap_KpnI_back and P5 upstream of pSB1C3_001_RC_insrepcap_KpnI_back

Investigator: Anissa
Digestion of the constructs:

P320 = pSB1C3_001_RC_insrepcap_KpnI_back c=408 ng/µL
P320 = pSB1C3_001_RC_insrepcap_KpnI_back c=408 ng/µL
P180 = pSB1C3_pTAV2 (P5)clone 1 c=108,8 ng/µL
P184 = pSB1C3_pAAV_RC (P5TATAless)clone 3 c=176,9 ng/µL

Components	v_{P320 upstream} /µL	v_{P180 upstream}/µL	v_{P320 downsteam} /µL	v_{P184 downsteam}/µL
DNA	2,5	13,8	2,5	8,5
BSA (10x)	1,5	2	1,5	1,5
Buffer no. 4 (10x)	1,5	2	1,5	1,5
Enzyme 1	XbaI 1	SpeI 1	SpeI 1	XbaI 1
Enzyme 2	EcoRI 1	EcoRI 1	PstI 1	PstI 1
H₂O	7,5	0,2	7,5	1,5
Total volume	15	20	15	15

Loading plan:

M    P320(upstream)    P320(downstream)    P180    P184

Results:

After gel extraction has been performed, the ligation was carried out.

Ligation:

v_{=P320_up}=7,37µL
v_{=P180_up}=0,63µL
v_{=P320_down}=7µL
v_{=P184_down}=1µL

The ligation mix was transformed into XL1-Blue cells and plated on agar plates containing chloramphenicol.

Next steps:
Picking clones and perform Mini-Prep.

Test digestion of VP2-N-terminal fusion constructs

Investigator: Hanna

Comment: On Satureday a colony PCR was performed of:
1. pCerulean_Zegfr:1907_ShortLinker_VP2/3 (P530)
2. pCerulean_Zegfr:1907_SEG_VP2/3 (P531)
3. pCerulean_CFP_MiddleLinker_VP2/3 (P532)
4. pCerulean_6xHis_MiddleLinker_VP2/3 (P533)
5. pCerulean_6xHis_MiddleLinker_VP2/3_insCap (P534)
6. pCerulean_Zegfr:1907_MiddleLinker_VP2/3_insCap (P535)

Because all constructs (4 clones of each approach), including the negative control (pAAV_RFC25), showed positive results, one test digestion of each construct was performed.

Digestion

components	Components Master Mix /µl
BSA (10x)	7
Buffer 4 (10x)	7
EcoRI	3.5
SpeI	3.5
H₂O	35

--> 2 µL DNA + 8 µL Master Mix

Incubation: 1.5 h

Agarose-Gel:

0.4 g Agarose, 50 mL TAE (0.8 %), 3 µL GELRED, at 100 Volt, running time: 50 minutes

Sample	Sample/µl]	Loading dye (6x)/µl	Expected size 1	Expected size 2
P 530	10 µl	2 µl	2710 bp	3937 bp
P 531	10 µl	2 µl	2710 bp	3937 bp
P 532	10 µl	2 µl	2710 bp	3937 bp
P 533	10 µl	2 µl	2710 bp	3937 bp
P 534	10 µl	2 µl	2710 bp	3937 bp
P 535	10 µl	2 µl	2710 bp	3937 bp

Marker: GeneRuler ladder mix

	Marker /µL	Sample P530 /µl	Sample P531 /µl	Sample P532 /µl	Sample P533 /µl	Sample P534 /µl	Sample P535 /µl
Lane	4	12	12	12	12	12	12

Test Digestion N-terminal VP2 Fusion

Comment: Test digestion delivered positive results: Expected fragment size after VP2/3 fusion to Zegfr:1907_Linker: 2180 bp - compared to failed VP2/3 insertion: ~ 220 bp.
Expected fragment size after VP2/3 fusion to CFP_MiddleLinker: 2710 bp - compared to failed VP2/3 insertion: ~ 760 bp.
pCerulean_ZEGFR:1907_Longlinker_VP2/3
pCerulean_CFP_Middlelinker_VP2/3_insCap
pCerulean_ZEGFR:1907_Shortlinker_VP2/3_insCap
pCerulean_ZEGFR:1907_Shortlinker_VP2/3
pCerulean_ZEGFR:1907_SEG_VP2/3
pCerulean_CFP_MiddleLinker_VP2/3
pCerulean_6xHis_MiddleLinker_VP2/3
pCerulean_6xHis_MiddleLinker_VP2/3_insCap
pCerulean_ZEGFR:1907_MiddleLinker_VP2/3_insCap
will be sent for sequencing to GATC.

BioBrick production: PCR of pAAV_RC_InsRepCap_KpnIback_VP1-ko and VP2-ko

Investigator: Stefan

DNA samples were diluted 1:1000

P455 = pAAV_RC_1.2 SDM SalI
P463 = pAAV_RC_CapIns_prepSDM clone 3

PCR progam:

Ingredients	Volume P455 / µl	Volume P463 / µl
5X Phusion HF buffer	10	10
10 mM dNTP mix	1	1
forward primer: O93	2,5	2,5
reverse primer: O115	2,5	2,5
DNA Template	3	3
DMSO	2	2
Phusion Polymerase	0,5	0,5
H₂O	28,5	28,5
Total volume	50	50

PCR program:

Cycles	Temperature / °C	Time / s
1	98	60
2 ( step 2-4: 8x)	98	15
3	59	25
4	72	75
5 (step 5-6: 17x)	98	15
6	72	85
7	72	300
Hold	4	4

Gel:
0,5 g agarose (1%), 50 ml TAE, 3µl GELRED running time: 45 minutes at 110V

Gel-Extraction:
Gel-extraction was performed according to standard protocol. The complete amount eluted was used for PCR digestion.

Digestion of PCR product:

Components	PCR products Volume/µL
DNA	30
BSA (10x)	4
Buffer no. 4 (10x)	4
EcoRI	1
SpeI	1
H₂O	-
Total volume	40

Digestion was performed at 37 °C for 2 hours.

PCR-Purification:
Gel-extraction was performed according to standard protocol.

c (P455) = 13,5 ng/µl
c (P463) = ng/µl

Digestion of plasmid backbone:
Plasmid used: pSB1C3_VCK_Bla (P320)
c (pSB1C3_VCK_Bla) = 408,0 ng/ µl

Components	vector Volume/µL
DNA	3
BSA (10x)	2
Buffer no. 4 (10x)	2
EcoRI	1
SpeI	1
H₂O	11
Total volume	20

Digestion was performed at 37 °C for 2 hours.

Gel:
0,5 g agarose (1%), 50 ml TAE, 3µl GELRED running time: 50 minutes at 120V

Gel-Extraction:
Gel-extraction was performed according to standard protocol.
c(P320) = 0,8 ng/µl

Ligation:

1 µl T4 DNA ligase
1 µl 10x Buffer
8 µl DNA mix (vector + insert)

Amounts of DNA used:

c(P320) = 7,73 µl
c(P455) = 0,27 µl

c(P320) = 7,19 µl
c(P463) = 0,81 µl

Incubation time: 45 minutes at room temperature.

Transformation:
Transformation was performed according to standard protocol using XL1b cells and Chloramphenicol as antibiotic.

2x repetition of CD biobrick

Investigator: Kira

Ingredients	CD sample
5X Phusion HF buffer	10 µl
10 mM dNTP mix	1µl
forward primer: O158	2,5µl
reverse primer: O159	2,5 µl
DNA Template (1:100 dil)	0,5 µl
DMSO	0 µl
Phusion Polymerase	0,5 µl
H₂O	33µl
Total volume	50 µl

PCR program:

Cycles	Temperature	Time
	98°C	1
10x	98°C	15"
	58°C	25"
	72°C	40"
17x	98°C	15"
	65°C	25"
	72°C	40"
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	0,5 µl
Enzyme 2 AgeI HF	0,5 µl
H₂O	10,8 µl
Total volume	20

incubation @ 37 C for approx. 6 h

1% agarose gel

According to the gel results, PCR was repeated twice.. But both tries revealed the same unexpected results. Insert from the last cloning procedure was found and used for the ligation and further transformation.

Ligation
T4 ligase was used
1 ul T4 Buffer
1 ul T4 Ligase
8 ul (0,9 ul vector+ 7,1 ul insert) DNA-mix

incubation @ RT for 45 min

Transformation was performed according to the standard protocol and the cells were spread on the agar plate containing Chloramphenicol.

126. labday 21.09.2010

Trafo evalutation of CD biobrick plate

Investigator: Kira

the agar plate was checked at approx. 4 pm and there were no colonies visible. Taking in account that the plate was incubated from 10.30 pm till 8 am @ 37C due to the electricity failure, the plate was put back @ 37C at 4.30 pm

Comment: the plate was picked this morning by a lab member and put in the coldroom

Continuation of cloning of pCerulean_Affibody_VP2/3 and pSB1C3_Affibody_middlelinker_GFP_his

Investigator: Jessica

Comment:Affibody_VP2/3 will be cloned in pCerulean and Affibody_middlelinker will be cloned together with GFP_His in pSB1C3

P407= pCerulean_CFP_middlelinker c=482,76 ng/µl
P516= pSB1C3_ZEGFR:1907_VP2/3 clone 1 c= 191,6 ng/µl
P290= pSB1C3_Affibody_Middlelinker clone 1 c= 227,4 ng/µl
P518= pSB1C3_GFP_RFC25_upper band clone 1 c= 138,3 ng/µl
P520= pSB1C3_GFP_RFC25_lower band clone 1 c= 141,6 ng/µl

Digestion:

components	P516	P518	P520
DNA	10	10	10
BSA (10x)	2	2	2
Buffer 4 (10x)	2	2	2
EcoRI	0,8	-	-
AgeI	0,8	-	-
MscI	0,8	-	-
NgoMIV	-	0,8	0,8
SpeI	-	0,8	0,8
H₂O	3,6	4,4	4,4
Total volume	20	20	20

0,5 g Agarose,50 ml TAE (1%), 3 µl GELRED , at 120 Volt

Gelextraction:

The gelextraction was performed according to the standard protocol. DNA concentration of the extracts:

P516= c= ng/µl
P518= c= ng/µl
P520= c= ng/µl

T4 Ligation:

The Ligation was performed as following:

Vector Volume: µl
Insert Volume: µl

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

Incubating for 40 minutes.

Transformation:

Trafo was performed according to the standard protocol (XL1blue). The cells were plated on a agar plate with Kana/Cm

Sequencing result of pSB1C3_EGFP_His upper and (!) lower band

Investigator: Jessica
1. pSB1C3_EGFP_His suffix:

2. pSB1C3_EGFP_His prefix:

results look in both plasmids and are used for cloning of pSB1C3_Affibody_middlelinker_GFP_His

Midi-Prep of pHelper & pSB1C3_leftITR_CMV_beta-globin_mVenus_hGH_rightITR

Investigators: Chris W.

Midi-Preps of pHelper=P540 and pSB1C3_leftITR_CMV_beta-globin_mVenus_hGH_rightITR=P541

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

plasmid-no.	P540	P541
concentration (ng/µl)	480,45	1264,20

New aliquots (60µl) of XL1blue can be used ! (Jessica)

127. labday 22.09.2010

Sequencing results of ViralBrick ligations using dephosphorylated vector

Investigator: Achim

Sequencing confirmed a correct sequence for clone 11.4 (453 Z34C). Clone 12.1 (587 Z34C)has several missing bases at the 3' end of the insert, clone 13.2 has an a -> c mutation and a c insertion in the insert (although the a->c might be a sequencing error.). Clone 14.2 contained a c deletion.

We have several new approaches:

-Correction of the mutations via PCR: We'll use the hybridisation oligo for the side of the insert containing the mutations, the rfc 25 primer on the other side. The amplified insert will be ligated into dephosphorized vector.

-As a backup, SDM-primers will be ordered and should be available next week.

-Also, a new colony pcr with several clones from the last ligation plates will be carried out.

-clone 13.4 (already prepped) will be sent for sequencing

Cloning pSB1C3_Viral Brick 587KO-empty (B274/P542) into pSB1C3_VP2/3_Capins (B438/P514)

Investigator Patrick
After an over night digestion with BamHI and PvuII at 37°C ....

My dear friend - what do you mean with "..."?? overnight digest at which temperature?? Did you look it up whether the enzymes show star activity at longer digestions or not?? ;-)

The Gelextraction with P514 was performed according to the standard protocol yielding 16,9 ng/ml.
The P542 insert should be 48 bp long and therefore was extracted with a QIAGEN kit able to extract even very small DNA fragments (40 bp) (QiaEX II Gel Extraction Kit (150)).

Expected size of the fragments:
P542: 2112 & 48 bp
P514: 3956 & 48 bp

The 48 bp band of P514 can't be seen clearly on the picture due to the bad resolution.

Ligation with T4 DNA ligase: 1 µl buffer (10x), 1 µl T4 DNA ligase, 7 µl Vector, 1 µl Insert, 70 minutes.

The transformation with XL1B was performed according to the standard protocol and plated: pSB1C3_VP2/3_Capins_587KO-empty

Cellculture: Serum-free cells

Investigator Patrick
We want our virus production to be serum-free to simplify the following purification.
15 ml cell-medium, 25% serum-free: 3,75 ml serum-free DMEM + 11,25 ml DMEM
15 ml cell-medium, 50% serum-free: 7,5 ml serum-free DMEM + 7,5 DMEM

PCR of P40

Investigator: Jessica
DNA sample P432 was diluted 1:1000

Ingredients	Volume / µl
5X Phusion HF buffer	10
10 mM dNTP mix	1
forward primer: O152	2,5
reverse primer: O188	2,5
DNA Template	3,0
DMSO	-
Phusion Polymerase	0,5
H₂O	31
Total volume	50,5

PCR program:

Cycles	Temperature / °C	Time / s
	98	60
8x	98	15
	61	25
	72	8
17x	98	15
	69	25
	72	8
1x	72	300
Hold	4

Digestion of plasmid backbone:
Plasmid used: pSB1C3_CFP (P51.2)
c (pSB1C3_CFP) = 151, 1 ng/ µl

Components	vector Volume/µL
DNA	10
BSA (10x)	2
Buffer no. 4 (10x)	2
XbaI	1
PstI	1
H₂O	4
Total volume	20

incubation @ 37 C for approx. 2 h

Comment:

Digestion of PCR product:

Components	PCR products Volume/µL
DNA	40
BSA (10x)	6
Buffer no. 4 (10x)	6
PstI	2
XbaI	2
H₂O	4
Total volume	60

Digestion was performed at 37 °C for 2 hours.

PCR-Purification:

c (P432) = 31,8ng/µl

Gel-Extraction:
Gel-extraction was performed according to standard protocol.
c(P51.2) = 3,7ng/µl

Ligation:

1 µl T4 DNA ligase
1 µl 10x Buffer
8 µl DNA mix (vector + insert)

Amounts of DNA used:

(P51.2) = 7,74 µl
(P432) = 0,26µl

Incubation time: 45 minutes at room temperature.

Transformation:
Transformation was performed according to standard protocol using XL1b cells and Chloramphenicol as antibiotic.

Mini-Prep of pSB1C3_001_RC_InsRepCap_KpnIback_VP1-ko

Investigator: Stefan

Comment:

Glycerol stocks were prepared:

B463 = pSB1C3_001_RC_InsRepCap_KpnIback_VP1-ko_P5tataless clone 1
B464 = pSB1C3_001_RC_InsRepCap_KpnIback_VP1-ko_P5tataless clone 2

Mini-Prep was performed according to standard protocol:

P548 = pSB1C3_001_RC_InsRepCap_KpnIback_VP1-ko_P5tataless clone 1 c = 435,82 ng/µl
P549 = pSB1C3_001_RC_InsRepCap_KpnIback_VP1-ko_P5tataless clone 2 c = 409,21 ng/µl

Cloning of CMV promotor into pSB1C3_VP123_inscap

Investigator: Anna

Vector name: pSB1C3_VP123_inscap P489
Insert name: pSB1C3_CMV P193
new vector name: pSB1C3_CMV_VP123_capins P580
buffer used: 4
DNA concentration (vector): 350,0 ng/µl ; DNA concentration (insert): 333,5 µg/µl

components	volume of pSB1C3_VP123_capins /µl	volume of pSB1C3_CMV /µl
DNA	3	4,5
BSA (10x)	1,5	1,5
Buffer 4 (10x)	1,5	1,5
Enzyme I	EcoI HF 1	EcoI HF 1
Enzyme II	XbaI 1	SpeI 1
H2O	7	5,5
Total volume (e.g. 15,20,25,30 µl)	15	15

0,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 120 Volt, running time:45

Loading plan for agarose gel:
Loading dye with SDS (6X), 3 µl
Marker used: GeneRuler ladder mix (Fermentas), 4 µl

	Marker	Sample 489, 18µl	Sample 193, 18µl
Lane	1	3	5
Fragment size		4404 bp	681 bp

Gel extraction:

	pSB1C3_VP123_capins_cut	CMV
DNA-concentration [ng/µl]	14,09	32,61

T4 Ligation:
Volume vector: 3,86 µl
Volume insert: 4,14 µl

Transformation:

Was performed following the standard protocol using XL1B cells.

Sequencing of Zegfr:1907-Linker Library, His-Tag and imaging appoaches

Investigator: Hanna

Comment: After several problems were managed (cloning difficulties, colony PCR troubles, interchanges of samples,...), sequences of the final constructs needed to be verified in order to test the constructs in cell culture.

Sample gallery
pCerulean_CFP_MiddleLinker_ VP2/3_InsCap (P528) forward	pCerulean_CFP_MiddleLinker_ VP2/3_InsCap (P528) reverse
pCerulean_ZEGFR:1907_ShortLinker_ VP2/3_InsCap (P527) forward	pCerulean_ZEGFR:1907_ShortLinker_ VP2/3_InsCap (P527) reverse
pCerulean_6xHis_MiddleLinker_ VP2/3 (P533) forward	pCerulean_6xHis_MiddleLinker_ VP2/3 (P533) reverse
pCerulean_6xHis_MiddleLinker_ VP2/3_insCap (P534) forward	pCerulean_6xHis_MiddleLinker_ VP2/3_insCap (P534) reverse
pCerulean_ZEGFR:1907_MiddleLinker_ VP2/3_insCap (P535) forward	pCerulean_ZEGFR:1907_MiddleLinker_ VP2/3_insCap (P535) reverse
pCerulean_ZEGFR:1907_SEG_ VP2/3_insCap (P502) reverse	pCerulean_ZEGFR:1907_LongLinker_ VP2/3_insCap (P503) reverse
pCerulean_ZEGFR:1907_MiddleLinker_ VP2/3 (P504) reverse

Comment: Sequences looked well. The 6 samples with VP2/3_insCap will be tested today in cell culture.

Mass Midi-Prep

Investigator: Chris W.

Midi-Prep of:

pSB1C3_001_RC_InsRepCap_KpnIback_P5tataless clone 1 =P544
pSB1C3_001_RC_InsRepCap_KpnIback_P5tataless clone 2 =P545
pSB1C3_001_P5_RC_InsRepCap_KpnIback clone 1 =P546
pSB1C3_001_P5_RC_InsRepCap_KpnIback clone 2 =P547
pHelper =P550
pHelper =P551
pSB1C3_litr_pTert_ßglobin_mvenus_hgh_ritr clone 1 =P552
pAAV_RC_RepCapIns_SDMKpnl_VP1ko clone 1 =P553
pAAV_RC_RepCapIns_SDMKpnl_VP2ko clone 1 =P554
pAAV_RC_RepCapIns_SDMKpnl_VP2ko clone 1 =P555
pCerulean_ZEGFR:1907_SEG_VP2/3_CapIns clone 3 =P556
pCerulean_ZEGFP:1907_LongLinker_VP2/3_CapIns clone 2 =P557
pCerulean_CFP_Middlelinker_VP2/3_insCap =P558
pCerulean_ZEGFR:1907_Shortlinker_VP2/3_insCap =P559
pCerulean_6xHis_MiddleLinker_VP2/3_insCap =P560
pCerulean_ZEGFR:1907_MiddleLinker_VP2/3_insCap =P561
pCerlulean_ZEGFR:1907_Shortlinker_VP2/3_insCap clone 4.8 =P562

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

plasmid-no.	P544	P545	P546	P547	P550	P551	P552	P553	P554	P555	P556	P557	P558	P559	P560	P561	P562
concentration (ng/µl)	1851,91	1822,3	1783,48	2625,57	1524,63	3333,48	2641,57	2165,22	1818,23	2318,58	3255,81	2818,15	2761,32	3289,23	3134,26	3725,27	1965,28

RNA isolation and cDNA synthesis

Investigator Kira

Motivation: in order to figure out if our cell lines do express telomerase, cell pellets were used for RNA isolation.

RNeasy Kit was used for RNA isolation. The cells were harvested and pellets washed 2x with PBS. add RLT buffer
homogenize the lysate with syringe ans blunt needle
add 1 volume of 70% EtOH
centrifuge for 15s @ 10.000 rpm
add 700 ul Buffer RW1 and centrifuge again
add 500 ul Buffer RPE and centrifuge
add 500 ul Buffer RPE and centifuge for 2 min
place the column in 1.5 ml tube and add RNase free water (50 ul)

concentrations:
c(293)= 41, 68 ng/ul
c(a431) = 135, 48 ng/ul

Gel apparatus (chamber, tray and comb) for RNA purity gel has to be prepared a day ahead with : water, SDS and NaOH

cDNA synthesis

Investigator: Kira

The yielded DNA was used for cDNA synthesis.
QuantiTect Reverse Transcription (Qiagen) reaction was performed according to the manufacturer protocol. DNA elimination reaction mix:

components	a431/µl	293/µl
7xgDNA Wipeout Buffer	2	2
Template RNA	1,6	2
RNase-free H2O	10,4	10
Total volume	14	14

Reverse-transcription reaction mix:

components	1xreaction	MM
Quantiscript Reverse Transcriptase	1	3
5x Quantiscript RT buffer	4	12
RT primer Mix	1	3
DNA elimination reaction mix	14	-
Total volume	20	-

incubation for 15 min @ 42C
incubation for 3 min @ 95C

128. labday 23.09.2010

PCR of VB constructs to remove mutations

Investigator Achim

Colony PCR of new clones from the last ligations

Investigator Achim

Sequencing of the previously picked clones revealed that the inserts were successfully cloned into pSB1C3. Sadly, apart from 453 Z34C every other insert contained various mutations (deletions, insertions, base exchanges in different positions). The reasons are unclear, probably difficulties with the fill in reaction or incorrectly synthesized oligos. We picked more clones from the last ligations' plates and carried out a colony pcr on them:

Contuniation: Cloning pSB1C3_Viral Brick 587KO-empty (B274/P542) into pSB1C3_VP2/3_Capins (B438/P514)

Investigator Patrick
3 Clones were picked in the morning and in each case inoculated 10 ml DYT. Clone 3 didnt grew fast enough. There were not enough bacteria in the eppi even after 8 ml were centrifuged. The mini-prep of clone 1 and 2 was performed according to the standrd protocol yielding the following concentrations:
Clone 1: 36,64 ng/µl
Clone 2: 7,8 ng/µl
Therefore only clone 1 was sent for sequencing (labelling: pat1, primer:VR2) and only this clone received a plasmid number: P569
No test-digestion was performed.
Because all medium was used to receive a sufficient amount of bacteria from clone 1 there was no cell suspension left to prepare a glycerol stock. Therefore again each clone was used to inoculated 10 ml DYT, following a mini-prep tomorrow.

Sequencing results:

Obviously there is something wrong with the backbone or the sequencing.

Mini-Prep and test digestion of pCerulean_Affibody_VP2/3, pSB1C3_Affibody_middlelinker_EGFP_His, pSB1C3_001_RC_InsRepCap_KpnIback_VP2-ko

Investigator: Jessica

Comment:

Glycerol stocks were prepared:

B465 = pCerulean_ZEGFR:1907_VP23 clone1
B466 = pCerulean_ZEGFR:1907_VP23 clone2
B467 = pSB1C3_ZEGFR:1907_middlelinker_EGFP_His clone1
B468 = pSB1C3_ZEGFR:1907_middlelinker_EGFP_His clone2
B469 = pSB1C3_001_RC_InsRepCap_KpnIbackVP2-KO clone1
B470 = pSB1C3_001_RC_InsRepCap_KpnIbackVP2-KO clone2

Mini-Prep was performed according to standard protocol:

P563 = pCerulean_ZEGFR:1907_VP23 clone1 = 227,4 ng/µl
P564 = pCerulean_ZEGFR:1907_VP23 clone2 = 337,2 ng/µl
P565 = pSB1C3_ZEGFR:1907_middlelinker_EGFP_His clone1 = 252,7 ng/µl
P566 = pSB1C3_ZEGFR:1907_middlelinker_EGFP_His clone2 = 209,5 ng/µl
P567 = pSB1C3_001_RC_InsRepCap_KpnIback_VP1-KO clone1 = 304,7 ng/µl
P568 = pSB1C3_001_RC_InsRepCap_KpnIback_VP1-KO clone2 = 383,1 ng/µl

Test digestion of

P563 = pCerulean_ZEGFR:1907_VP23 clone1

P564 = pCerulean_ZEGFR:1907_VP23 clone2

P565 = pSB1C3_ZEGFR:1907_middlelinker_EGFP_His clone1

P566 = pSB1C3_ZEGFR:1907_middlelinker_EGFP_His clone2

Components	P563-566 Volume/µL
DNA	2
BSA (10x)	1
Buffer no. 4 (10x)	1
PstI	0,5
XbaI	0,5
H₂O	5
Total volume	10

Results:

P566 = P565 ; P567 = P566 - P566 is not OK!!!
P563 and P566 was sent for sequencing with primer VF2 and VF2/VR2

PCR for 587 Z34C ViralBricks

Investigators: Achim, Anna

Plasmids used as template:

12_T4_1: c = 80,36 ng/µl
13_T4_2: c = 80,87 ng/µl
14_T4_2: c = 98,52 ng/µl

Primer used:

Template	Primer for	Primer rev
12_T4_1	RFC25	O146
13_T4_2	RFC25	O148
14_T4_2	O149	RFC25

Ingredients	Volume / µl
5X Phusion HF buffer	10
10 mM dNTP mix	1
forward primer: see above	2,5
reverse primer: see above	2,5
DNA Template (1:100 dilution)	1,0
DMSO	1,0
Phusion Polymerase	0,5
H₂O	31,5
Total volume	50

PCR program:

Cycles	Temperature / °C	Time / s
	98	60
	98	15
25x	68	25
	72	10
1x	72	300
Hold	4°C

Digestion of samples:

Restriction enzymes used: BamHI and PvuI.

Comment:

PCR of Vp1_ex, Vp2_ex and Vp3_ex and cloning into pSB1C3_001

Investigator: Anissa

DNA sample P72 (pkex_Vp1), P73(pkex_Vp2) and P74(pkex_Vp3) were diluted 1:100
used primers: O89 = Präfix_Vp1ex, O90= Präfix_Vp2ex, O91= Präfix_Vp2ex, O92= Suffix_Vp123ex, O120= Suffix_Vp123ex_reg

Ingredients	Volume / µl
5X Phusion HF buffer	10
10 mM dNTP mix	1
forward primer: O152	2,5
reverse primer: O188	2,5
DNA Template	2,0
DMSO	1
Phusion Polymerase	0,5
H₂O	30,5
Total volume	50

PCR program:

Cycles	Temperature / °C	Time / s
1x	98	60
25x	98	15
25x	60	25
25x	72	55
1x	72	5
Hold	4

Comment:The primer O120 was firstly given to the samples. It's a different primer for the Vp123_suffix, which binds to the regulatory-sequence. Because there was no knowledge, if the Vp_ex constucts have this sequence or not, O92 was also given to the samples.

Comment:Because gel-picture showed only DNA within the gel-bags, PCR was repeated.

Digestion of plasmid backbone:
Plasmid used: pSB1C3_001 (P320)
c (pSB1C3_001) = 408 ng/ µl

Components	vector Volume/µL
DNA	2,5
BSA (10x)	1,5
Buffer no. 4 (10x)	1,5
SpeI	1
NgomIV	1
H₂O	7,5
Total volume	15

incubation @ 37 C for approx. 1,5 h

Comment:Strangely, PCR-products did not run into the gel, altough the PCR was repeated, after first PCR had two reverse primers in the sample. This could be because of a complex with the polymerase.However, ligation will be continued with the DNA within the bags.

</br>

Digestion of PCR product:

Components	PCR products Volume/µL
DNA	20
BSA (10x)	3
Buffer no. 4 (10x)	3
SpeI	1
NgomIV	1
H₂O	2
Total volume	30

Digestion was performed at 37 °C for 2 hours.

PCR-Purification:

was peformed according the standard-protocol.

c (P432) =-- ng/µl

Comment:THE WHOLE PCR WILL BE REPEATED ONCE AGAIN

RNA Purity Gel

Investigator: Kira
10x FA buffer: 200mM MOPS, 50mM Sodium Acetat, 10mM EDTA, RNase free water
1x FA running buffer: 10x FA buffer, 37% Formamid, RNAase free water

Agarose gel: Agarose 0,6 g; 10x FA Buffer 5ml; RNAse free water 45ml; 37% Formamid 0,9 ml

hTERT PCR Reaction

Investigator: Kira

@Kira: Do you think that we can (suggestion?) use the A431 for detection of gene expression driven by phTERT promoter?? We should keep in mind that the transduction efficieny will not be that well ;-) (Bea)

Ingredients	Volume / µl
10x PCR buffer	2
10 mM dNTP mix	0,4
50mM MgCl2	0,6
Primer 1	0,5
Primer 2	0,5
cDNA template	1
Taq Polymerase	0,1
H₂O	14,9
Total volume	20

PCR program:

Cycles	Temperature / °C	Time
1x	94	3min
30x	94	45sec
	51	30
	72	1min 30sec
1x	72	10
Hold	4

1% agarose gel:

Evaluation: The agarose gel reveals that all samples show telomerase activity but in different levels.

Cloning of pBAD_Affibody_middlelinker_EGFP_His

Investigator: Jessica

Vector: name: pBAD_ OmpA His FluA LL Foki PGerrit
Insert: name: pSB1C3_ZEGFR:1907_middlelinker_EGFP_His P566
new vector name: pBAD_ZEGFR:1907_middlelinker_EGFP_His P
buffer used: 4
DNA concentration (vector): 97,0 ng/µl ; DNA concentration (insert): 209,5 µg/µl

components	volume of pBAD_ OmpA His FluA LL Foki /µl	volume of pSB1C3_ZEGFR:1907_middlelinker_EGFP_His /µl
DNA	10	6
BSA (10x)	2	2
Buffer 4 (10x)	2	2
Enzyme XbaI	0,8	0,8
Enzyme AgeI	0,8	0,8
H2O	4,4	8,4
Total volume (e.g. 15,20,25,30 µl)	20	20

0,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 120 Volt

Loading plan for agarose gel:
Loading dye with SDS (6X), 3 µl
Marker used: GeneRuler ladder mix (Fermentas), 6 µl

	Marker	Sample PGerrit, 20µl	Sample 566, 20µl
Lane	1	3	5
Fragment size		4047 bp	963 bp

Gel extraction:

	pBAD	Affibody_middlelinker_EGFP_His
DNA-concentration [ng/µl]	8,3	10,2

T4 Ligation:
Volume vector: 5,06 µl
Volume insert: 2,94 µl

Transformation:

XL1B cells were used.

Picking clones of pSB1C3_CMV_VP123_inscap

Investigator: Anna

Three clones were picked (10 ml DYT, 10 µl Cm).

Cloning of * into pSB1C3_CFP

Investigator: Chris W.

Vector: name: pSB1C3_CFP P51,2
Insert: name: email Hybrid Oligo (O184&O185)
new vector name: pSB1C3_email
buffer used: 4
DNA concentration (vector): 151,0 ng/µl ; DNA concentration (insert): 95,3 µg/µl

Interesting, where does the promoter come from the new annotared vector?? ;-)

components	volume of pSB1C3_CFP /µl	volume of email/µl
DNA	6	15
BSA (10x)	2	2
Buffer 4 (10x)	2	2
Enzyme I	NgoMIV 1	NgoMIV 1
Enzyme II	SpeI 1	SpeI 1
H2O	8,4	-
Total volume (e.g. 15,20,25,30 µl)	20	20

0,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 120 Volt, running time:45

Loading plan for agarose gel:
Loading dye with SDS (6X), 4 µl
Marker used: GeneRuler ladder mix (Fermentas), 3 µl

	Marker	Sample Insert, 20µl	Sample Vector, 20µl
Lane	1	3	5
Fragment size		70 bp	2070 bp

Gel extraction:

	pSB1C3_CFP_cut	email
DNA-concentration [ng/µl]	7,8	27,4

T4 Ligation:
Volume vector: 8,74 µl
Volume insert: 0,26 µl

Transformation:

XL1B cells were used.

Repetition: Cloning of P5_TATAless downstream of pSB1C3_001_RC_insrepcap_KpnI_back and P5 upstream of pSB1C3_001_RC_insrepcap_KpnI_back

Investigator: Stefan
Digestion of the constructs:

P432 = pSB1C3_001_RC_insrepcap_KpnI_back c=344,5 ng/µl
P432 = pSB1C3_001_RC_insrepcap_KpnI_back c=344,5 ng/µl
P180 = pSB1C3_pTAV2 (P5)clone 1 c=108,8 ng/µl
P184 = pSB1C3_pAAV_RC (P5TATAless)clone 3 c=176,9 ng/µl

My dear friend, did you mix up the Rep-Cap constructs in the plasmid list? P432 = pAAV_RC_insRepCap_KpnI-back ;)

Components	V P432up /µL	VP180up /µL	V P432down /µL	V P184down /µL
DNA	4,5	14	4,5	11
BSA (10x)	2	2	2	2
Buffer no. 4 (10x)	2	2	2	2
Enzyme 1	XbaI 1	SpeI 1	SpeI 1	XbaI 1
Enzyme 2	EcoRI 1	EcoRI 1	PstI 1	PstI 1
H₂O	9,5	9,5	-	3
Total volume	20	20	20	20

Results:

Gel-Extraction: Gel-Ex was performed according to protocol. The following concentrations were measured:

432up c= 25,73 ng/µl
180up c= 9,57 ng/µl
432down c= 27,34 ng/µl
184down c= 17,80 ng/µl

Ligation:
The following DNA mixes were used for ligation:

432up V= 6,3 µl
180up V= 1,7 µl

432down V= 6,93 µl
184down V= 1,07 µl

Transformation:
The transformation was performed according to standard protocol using BL21 cells. They were plated on agar plates containing chloramphenicol and stored in 37°C room overnight.

129. labday 24.09.2010

Sequencing results of VB 13.4

Investigator: Achim

We sent in another clone of the 587 KO Z34C motif to see if it carries the same mutations as the first one. If that had been the case, we could account the mutations to faulty oligos. However, sequencing showed that the second 587 KO Z34C clone is mutated as well, but in different positions. So we either recieved oligos containing various mutations, or the fill-in reaction was faulty in spite of the proofreading activity of the klenow fragment.

Because 587 KO Z34C is one of our more promising approaches, we sent another two clones from our second colony pcr/clone picking round for sequencing: 13.1 and 13.4

Contuniation: Cloning pSB1C3_Viral Brick 587KO-empty (B274/P542) into pSB1C3_001_VP2/3_Capins (B438/P514)

Investigator Patrick
Because of the sequencing results of clone 1 a mini-prep was performed only with clone 2 and 3 yielding the following concentrations:
pSB1C3_VP2/3_Capins_587KO-empty clone 2: 195 ng/µl
pSB1C3_VP2/3_Capins_587KO-empty clone 3: 224,74 ng/µl

Testdigestion:
pSB1C3_VP2/3_Capins_587KO-empty clone 2 (P578/B472): 3 µl Buffer 4, 0,5 µl BamHI, 0,5 µl PvuII, 22 µl DNA, 4 µl H2O
pSB1C3_VP2/3_Capins_587KO-empty clone 3 (P579/B473): 23 µl Buffer 4, 0,5 µl BamHI, 0,5 µl PvuII, 20 µl DNA, 6 µl H2O
Because somebody switched the 37°C thermoblock off i dont know the exact digestion time. Therefore i switched the thermoblock on again and waited 1 hour. I used that much DNA because the desired insert is 48 bp long.

Clone 3 was sent for sequencing.

Sequencing evaluation of VP2/3_Gsat-linker and VP2/3_cap_Gsat-linker

Investigator Kira

Comment: pSB1C3_VP2/3_cap_Gsat-linker as well as pSB1C3_VP2/3_Gsat-linker can be used for further experiments.

New CD primer ordered

Investigator Stefan

Comment: CD reverse primer was incorrect. A new primer was ordered.

Sequencing of pCerulean_Zegfr:1907_VP2/3

Investigator Hanna

Because I found out, that this plasmid was sent to GATC with the wrong sequencing primers (therefore no sequencing results were available), I sent it again with the GATC_std_CMV-F primer.
--> backbone = pCerulean and not pSB1C3!!! ;)

Repetition: PCR for biobrick production: Cloning RepCap into pSB1C3

Investigator: Stefan

Comment: Construct was cloned mixed RFC10 and RFC25. Therefore, a new approach will be performed consisting of RFC10 only.

Plasmid used:

pAAV_RC_RepCapIns_SDMKpnI (P432) A 1:1000 dilutionof the plasmid was prepared.

PCR protocol:

Ingredients	P432 (v/µl)
5X Phusion HF buffer	10
10 mM dNTP mix	1
forward primer: O93	2,5
reverse primer: O121	2,5
DNA Template	3
DMSO	-
Phusion Polymerase	0,5
H₂O	30,5
Total volume	50

PCR program:

Cycles	Temperature /°C	Time /s
1	98	60
2 (8x step 2-4)	98	15
3	59	25
4	72	70
5 (17x step 5-6)	98	15
6	72	80
71x	72	300
Hold 4°C

Digestion of the vector:

components	pSB1C3_VCK_Bla (P320) (v/µl)
DNA	3,5
BSA	2
Buffer 4 (10x)	2
SpeI	1
EcoRI	1
H₂O	10,5
Total volume	20

Comment:Digestion was performed 2 hours at 37 °C.

Gel:
0,5 g Agarose,50 ml TAE (1%), 3 µl Gelred , at 110 Volt; run for ~50 minutes

Gelextraction:

The gelextraction was performed according to the standard protocol. DNA concentration of the vector:

pSB1C3 (P320): c= 8,5 ng/µl

Digestion of the PCR-products:

components	PCR product (v/µl)
DNA	30
BSA	4
Buffer 4 (10x)	4
SpeI	1
EcoRI	1
H₂O	-
Total volume	40

Comment:Digestion was performed 2 hours at 37 °C.

PCR purification:
Purification was performed accoding to the standard protocol. The following concentrations were measured:

PCR of P432: c= 6,4 ng/µl

Ligation:
1 µl T4 Ligase buffer (2x) 8 µl DNA mix 1 µl T4 Ligase
Incubating for 45 minutes at room temperature.

The Ligation was performed using the following amounts of DNA:

Vector Volume: 0,92 µl
Insert Volume: 7,08 µl

Transformation:

Trafo was performed according to the standard protocol using XL1b cells. The cells were plated on a agar plates containing chlorampenicol.

Picking clones of pSB1C3_CFP_email

Investigator: Anna

Three clones were picked (10 ml DYT, 10 µl Chloramphenicol).

MiniPreps and Test digestion of pSB1C3_CMV_VP123_capins

Investigator: Anna

Sample	Concentration [ng/µl]
pSB1C3_CMV_VP123_capins_clone1	377,29
pSB1C3_CMV_VP123_capins_clone2	369,92
pSB1C3_CMV_VP123_capins_clone3	387,57

Test digestion:

Components	Volume /µl
DNA	2
BSA	-
Buffer 4 (10x)	1
EcoRI	0,5
NgoMIV	0,5
H₂O	6
Total volume	10

Expected size (CFP): 681 bp

Comment: Clone 1 was sent for sequencing with the following primers: VF2, 4000 for, 4200 rev, 2800 for and 2800 rev.

MiniPreps of 587 Z34C ViralBricks and pSB1C3_p40

Investigator: Anna

Sample	Clone	Concentration [ng/µl]
pSB1C3_587_KO_Z34C	13.1	266,97
pSB1C3_587_KO_Z34C	13.4	277,47

Comment: Both clones were sent for sequencing.

Sample	Clone	Concentration [ng/µl]
pSB1C3_p40	1	266,97
pSB1C3_p40	2	277,47
pSB1C3_p40	3	167,20

Re-Trafo of DARPin

Investigator Stefan

Comment: A Re-Trafo of the synthesized DARPin was performed using XL1b cells.

130. labday 25.09.2010

Sequencing of VB: 13.1, 13.4 (approach w. dephosphorylated vector, second clone picking round

Investigator: Achim

The two clones that were sequenced both contained a deletion in the same position in the insert. We really seem to have bad luck picking clones. Hopefully our PCR attempt works better.

Miniprep of serveral constructs

Investigator: Jessica

Glycerol stocks were prepared:

B489 = pBAD_EGFP_His clone1
B490 = pBAD_EGFP_His clone2
B491 = pBAD_EGFP_His clone3
B492 = pSB1C3_CFP_email clone 1
B493 = pSB1C3_CFP_email clone 2
B494 = pSB1C3_CFP_email clone 3

Mini-Prep was performed according to the standard protocol

P588= pBAD_EGFP_His clone1 c=71,0 ng/µl
P589 = pBAD_EGFP_His clone2 c=74,8 ng/µl
P590 = pBAD_EGFP_His clone3 c=58,3 ng/µl
P591 = pSB1C3_CFP_email clone 1 c=132,7 ng/µl
P592 = pSB1C3_CFP_email clone 2 c=168,9 ng/µl
P593 = pSB1C3_CFP_email clone 3 c=153,6 ng/µl

Test digestion:

Components	Volume P588-590 /µl	Volume P591-593 /µl	Volume P583-585 /µl
DNA	4,5	2,5	2
BSA	1	1	1
Buffer 4 (10x)	1	1	1
XbaI	0,4	0,4	0,4
PstI	0,4	0,4	0,4
H₂O	2,7	4,7	5,2
Total volume	10	10	10

Expected size : bp

Comment: test digestion of P591-593 and P583-585 (pSB1C3_P40) is just an attempt because I can't find any sequences in geneious.P583 looks well. P591, P588 and P583 will be sent for sequencing on monday.

Sequencing results of pSb1C3_Affibody_middlelinker_EGFP_His

Comment: there was anywhere a problem in the cloning process. approach will be repeated today. there is pBAD_EGFP_His, affibody_middlelinker will be cloned in, also in pSB1C3_EGFP_His

Sequencing result of pSB1C3_CMV_VP123_capins_clone1

Investigators: Volker, Anna

For test digestion go to labday 24.09.10

Comment: The following primers were used for sequencing: VF2, 4000 for, 4200 rev, 2800 for and 2800 rev. There is a point mutation in the non-coding sequence, which should not influence the performence of the construct, so it can be used for further cloning steps.

Cloning of 453 and 587 ViralBricks into pSB1C3_CMV_VP123_capins

Investigators: Achim, Anna

Vector name: pSB1C3_CMV_VP123_capins P580
Inserts: different ViralBricks (see pdf underneath), pSB1C3_VCK_Bla P320
buffer used: 4

Update: ViralBricks ready to use:

media:Freiburg10_Production of ViralBricks_new.pdf

Digestion of vector and inserts:

media:Freiburg10_Cloning of ViralBricks into pSB1C3_CMV_VP123_capins.pdf

The vector p580 was dephosphorylated.
Two gels were prepared with 1 g Agarose, 100 ml TAE (1%) and 6 µl GELRED; at 120 Volt, running time:45

Gel run:
Loading dye(6X), 6 µl
Marker used: GeneRuler ladder mix (Fermentas), 3 µl

Expected sizes of fragments: see Pdf under Gel extraction and overnight T4 Ligation

Gel extraction and overnight T4 Ligation:

media:Freiburg10_Cloning of ViralBricks into pSB1C3_CMV_VP123_capinsII.pdf

Sequencing results: pSB1C3_001_VP2/3_HSPG-KO

Investigator: Hanna

Comment: In order to knock down the natural tropism of the virus, the HSPG knock-out motif (two aa exchanges) was cloned into VP2/3. This fragment can then be used for the VP2 N-terminal fusion or VP1 insertion approaches.

Conclusion: Sequencing results looked well: The HSPG-KO ViralBrick was cloned successfully into VP2/3.

Cloning of pBAD_Affibody_middlelinker_EGFP_His and pSB1C3_Affibody_middlelinker_EGFP_His

Investigator: Jessica
Comment: There was a mistake in cloning pSB1C3_Affibody_middlelinker_EGFP_His so there is just pSB1C3_EGFP_His. in this plasmid will be cloned Affibody_middlelinker, also in pBAD_EGFP_His

Vector: name: pBAD_EGFP_His P588
Vector: name: pSB1C3_EGFP_His P565
Insert: name: pSB1C3_ZEGFR:1907_middlelinker_ P290
new vector name: pBAD_ZEGFR:1907_middlelinker_EGFP_His P
new vector name: pSb1C3_ZEGFR:1907_middlelinker_EGFP_His P
buffer used: 4
DNA concentration (vector): 71,0 ng/µl / 252,7 ng/µl; DNA concentration (insert): 227,4 µg/µl

components	volume of pBAD_EGFP_His /µl	volume of pSB1C3_EGFP_His /µl	volume of pSB1C3_ZEGFR:1907_middlelinker /µl
DNA	15	4	7
BSA (10x)	2	2	2
Buffer 4 (10x)	2	2	2
Enzyme XbaI	0,8	0,8	0,8
Enzyme AgeI	-	-	0,8
Enzyme NgoMIV	0,8	0,8	-
H2O	-	10,4	7,4
Total volume (e.g. 15,20,25,30 µl)	20,6	20	20

0,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 120 Volt

	Marker	P290, 20µl	P565, 20µl	P588, 20µl
Sample	4	1	2	3
Fragment size		210 bp	2800 bp	4700 bp

Gel extraction:

	pBAD	pSB1C3	Affibody_middlelinker
DNA-concentration [ng/µl]

T4 Ligation pBAD:
Volume vector: 3,5 µl
Volume insert: 4,5 µl

T4 Ligation pSB1C3:
Volume vector: 2,3 µl
Volume insert: 5,7 µl

131. labday 26.09.2010

Continuation of cloning of pBAD_Affibody_middlelinker_EGFP_His and pSB1C3_Affibody_middlelinker_EGFP_His

Transformation:

BL21 cells were used - in 37°C at 8.30am

pBAD_Affibody_middlelinker_EGFP_His
pSB1C3_Affibody_middlelinker_EGFP_His

Comment:pSB1C3_Affibody_middlelinker_EGFP_His was not successful (no colonies on plate), will be repeated on monday

Picking clones of different constructs

Investigator: Anna

Clones were picked of:

pBad_Affibody_middlelinker_EGFP_His
pSB1C3_001_RC_InsRepCap_KpnIback_RFC10
Darpin (ReTrafo)
pSB1C3_453_BAP (p402, ReTrafo)
pSB1C3_587_KO_RGD (p390, ReTrafo)
pSB1C3_587_KO_His (p391, ReTrafo)

In addition, preparations for Mini-Preps of several ViralBricks were done:

B289: 587_BAP
B270: 587_KO_BAP
B271: 587_RGD
B272: 453_His
B273: 587_His
B274: 587_KO_empty
B488: 453_Z34C

Comment: Inoculating of 10 mL DYT medium containing 10µL chloramphenicol (except pBad with Amp).
There were no clones on the plate with pSB1C3_Affibody_middlelinker_EGFP_His.

Continuation of cloning of 453 and 587 inserts into pSB1C3_CMV_VP123_capins

Investigator: Achim, Anna

Transformation:

Trafo was performed according to the standard protocol using XL1b cells. The cells were plated on agar plates containing chlorampenicol and stored in the 37°C room.

Colony PCR of remaining 587 constructs

Investigator: Achim, Anna

Comment: New clones of the remaining 587 constructs were picked (from new cloning approach with T4 Ligation and dephosphorylated vector, see labdays 15.09. and 22.09.).

Constructs:

12: 587_Z34C
13: 587_KO_Z34C
14: 587_Z34C_KO_Spacer

Components	Volume /µl
10x Standard Taq Buffer (with MgCl2)	1
MgCl2 (50mM)	0,1
dNTPs	0,2
Primer 1: RFC25 for	0,2
Primer 2: RFC25 rev	0,2
Taq Polymerase	0,05
H2O	8,25
Total volume	10

Cycles	Temperature	Time
	95°C	6 min
30x	95°C	25 sec
(Tm -3°C)	60°C	30 sec
1 min/kb	68°C	55 sec
1x	68°C	5 min
Hold 4°C

Clone 13.3, 14.1 and 14.3 will be sent for sequencing.

Sequencing results: pCerulean_Zegfr:1907_VP2/3

Investigator: Hanna

Sequencing results revealed that VP2/3 (unmodified!) was successfully fused to the Affibody (without linker).
Next step: Fusion of VP2/3-HSPG-KO to the C-terminus of the Affibody.

N-terminal VP2-Fusion & VP1 Insertion: Fusion of VP2/3_HSPG-KO

Investigator: Hanna

Comment: In order to target tumor cells with our AAV2 two VP2 fusion strategies were figuered out: The so called VP2-fusion and VP1 insertions. These approaches were successfully cloned and are now tested in cell culture. In order to prevent targeting of other (healthy) cells, the natural tropism of the virus needs to be knocked down. For this purpose a ViralBrick, "587-KO_empty", was designed and cloned into pSB1C3_001_VP2/3_Capins.
Today this VP2/3_HSPG-KO sequence will be fused to the N-terminus of the Affibody, CFP/mVenus and His-Tag of both, the N-terminal fusion to VP2 and the VP1 insertion, approach.

DIGESTION:

1. pCerulean_CFP_MiddleLinker (P407)
2. pCerulean_Z_EGFR:1907_MiddleLinker (P408)
3. pCerulean_Z_EGFR:1907_SEG (P409)
4. pCerulean_Z_EGFR:1907_ShortLinker (P410)
5. pCerulean_Z_EGFR:1907_LongLinker (P412)
6. pCerulean_6xHis_MiddleLinker (P374)
7. pCerulean_VP1up_NLS_Z_EGFR:1907 (P422)
8. pCerulean_VP1up_NLS_6xHis (P424)
9. pCerulean_VP1up_NLS_mVenus (P426)
10.1 pSB1C3_001_Vp2/3_HSPG-KO (P579)
10.2 pSB1C3_001_Vp2/3_HSPG-KO (P579)

Incubation: 2 hours, 37°C.
Agarose gel: 0.8%

Sample	Sample/µl]	Loading dye (6x)/µl	Expected size
1	20 µl	4 µl	4710 bp
2	20 µl	4 µl	4169 bp
3	20 µl	4 µl	4254 bp
4	20 µl	4 µl	4158 bp
5	20 µl	4 µl	4181 bp
6	20 µl	4 µl	2129 bp
7	20 µl	4 µl	4583 bp
8	20 µl	4 µl	4428 bp
9	20 µl	4 µl	5124 bp
10.1	20 µl	4 µl	1937 bp
10.2	20 µl	4 µl	1937 bp

Marker: GeneRuler ladder mix

	Marker /µL	Sample 1 /µl	Sample 2 /µl	Sample 3 /µl	Sample 4 /µl	Sample 5 /µl	Sample 6 /µl	Sample 7 /µl	Sample 8 /µl	Sample 9 /µl	Sample 10.1 /µl	Sample 10.2 /µl
Lane	4.5	24	24	24	24	24	24	24	24	24	36	36

LIGATION:

TRAFO:
Trafo was performed following our standard protocol. Cells: XL1b, DNA: 2µL.
Plates will be stored over night @ the 37°C room.

Next step: Picking 2 clones of each construct, colony PCR!

132. labday 27.09.2010

Sent for sequencing

Investigator: Jessica

P591 pSB1C3_email: VR2
P583 pSB1C3_P40: VR2
P588 pBAD_EGFP_His: pBAD-FP
P596 pBAD_Affibody_middlelinker_EGFP_His: pBAD-FP / pTrcHis-RP

Picking clones of VP1 insertion and VP2 fusion HSPG-KO approaches

Investigator: Hanna
2 clones were picked of each ligation approach = 18 falcons (Kanamycin).

To do: Mini-Prep and test digestion - sequencing.

MiniPreps of different constructs

Investigator: Anna

The following constructs were prepped according to the standard protocol:

pSB1C3_453_BAP (p402, ReTrafo)
pSB1C3_587_KO_RGD (p390, ReTrafo)
pSB1C3_587_KO_His (p391, ReTrafo)
B289: 587_BAP
B290: 453_RGD
B270: 587_KO_BAP
B271: 587_RGD
B272: 453_His
B273: 587_His
B274: 587_KO_empty
B488: 453_Z34C

B473:

Miniprep of serveral constructs

Investigator: Stefan

Glycerol stocks were prepared:

B489 = pSB1C3_001_RC_InsRepCap_KpnIback_RFC10 clone 1
B490 = pSB1C3_001_RC_InsRepCap_KpnIback_RFC10 clone 2
B491 = pBAD_Affibody_middlelinker_EGFP_His clone 1
B492 = pBAD_Affibody_middlelinker_EGFP_His clone 2
B493 = pBAD_Affibody_middlelinker_EGFP_His clone 3

Mini-Prep was performed according to the standard protocol

P594= pSB1C3_001_RC_InsRepCap_KpnIback_RFC10 clone 1 c= 140,9 ng/µl
P595 = pSB1C3_001_RC_InsRepCap_KpnIback_RFC10 clone 2 c= 117,5 ng/µl
P596 = pBAD_Affibody_middlelinker_EGFP_His clone 1 c= 101,4 ng/µl
P597 = pBAD_Affibody_middlelinker_EGFP_His clone 2 c= 92,9 ng/µl
P598 = pBAD_Affibody_middlelinker_EGFP_His clone 3 c= 92,1 ng/µl

Test digestion:

Components	Volume P594+P595 /µl	Volume P596-598 /µl
DNA	2,5	2,5\|
BSA	1	1
Buffer 4 (10x)	1	1
XbaI	0,4	0,4
PstI	0,4	0,4
H₂O	4,7	4,7
Total volume	10	10

Comment:

Re-Trafo of pSB1C3_pTAV (P5)

Investigator: Stefan

Comment:After inocculating from glycerol-stock, the plasmid showed strange results during digestion. Therefore a re-trafo will have to be performed to replace the stock.

Repetition: Cloning of P5_TATAless downstream of pSB1C3_001_RC_insrepcap_KpnI_back and P5 upstream of pSB1C3_001_RC_insrepcap_KpnI_back

Investigator: Stefan
Digestion of the constructs:

P594 = pSB1C3_001_RC_insrepcap_KpnI_back c=344,5 ng/µl
P594 = pSB1C3_001_RC_insrepcap_KpnI_back c=344,5 ng/µl
P586 = pSB1C3_pTAV2 (P5)clone 1 c=137,37 ng/µl
P587 = pSB1C3_pAAV_RC (P5TATAless)clone 3 c=191,61 ng/µl

Components	V P594up /µL	VP586up /µL	V P594down /µL	V P587down /µL
DNA	10	14	10	13
BSA (10x)	2	2	2	2
Buffer no. 4 (10x)	2	2	2	2
Enzyme 1	XbaI 1	SpeI 1	SpeI 1	XbaI 1
Enzyme 2	EcoRI 1	EcoRI 1	PstI 1	PstI 1
H₂O	9,5	9,5	-	3
Total volume	20	20	20	20

Results:

Comment:P5 and P5TATAless do not fit the expected results. For P5TATAless, a new digestion using the P184 plasmid was performed. For P5 no old plasmid stock was available, therefore a re-trafo will have to be performed.

Components	V P184down /µL
DNA	10
BSA (10x)	2
Buffer no. 4 (10x)	2
XbaI	1
PstI	1
H₂O	4
Total volume	20

Comment:No gel picture available because computer crashed completely...

Gel-Extraction:
Gel-Ex was performed according to protocol. The following concentrations were measured:

594down c= 29,9 ng/µl
184down c= 3,8 ng/µl

Ligation:
The following DNA mixes were used for ligation:

432down V= 4,48 µl
184down V= 3,52 µl

Transformation:
The transformation was performed according to standard protocol using BL21 cells. They were plated on agar plates containing chloramphenicol and stored in 37°C room overnight.

Picking clones of VP1 insertion and VP2 fusion HSPG-KO approaches

Investigator: Hanna
2 clones were picked of each ligation approach = 18 falcons (Kanamycin).

To do: Mini-Prep and test digestion - sequencing.

Picking clones of VP1 insertion and VP2 fusion HSPG-KO approaches

Investigator: Hanna
2 clones were picked of each ligation approach = 18 falcons (Kanamycin).

To do: Mini-Prep and test digestion - sequencing.

133. labday 28.09.2010

Cloning of the ViralBricks BAP-HSPG-ko and His-HSPG-ko into pSB1C3_VP2/3

Investigator: Bea

Comment: After discussing the finals constructs, we decided to clone HSPG-KO with BAP and His motifs into the N-terminal approaches which means that the plasmids pCerulean_Targeting_VP2/3 contains His and BAP ViralBricks integrated in the 587 loop, respectively. Therefore I started the first cloning step in order to obtain the fully assembled targeting construct which can be cotransfected with the plasmids containing rep and cap genes (with or wihtout HSPG-ko)

Digestion of the constructs:

P604 = pSB1C3_001_587-ko_BAP
P606 = pSB1C3_001_587-ko_His
P525 = pSB1C3_001_VP2/3capins

Components	v_P606 /µL	v_{P525 upstream}/µL	v_P604 /µL
DNA	21	6	18
BSA (10x)	4	2	4
Buffer no. 4 (10x)	4	2	4
Enzyme 1	BamHI	BamHI	BamHI
Enzyme 2	SpeI	PvuII	PvuII
H₂O	9	8	12
Total volume	40	20	40

Loading plan of a 1% agarose gel:

M    P525

Loading plan of a 2% agarose gel:

M    P604    P606

Expected sizes of the digested products are:

P525= 48,3800 bp
P604= 2216, 81bp
P606 = 2216, 108bp

Results:

Freiburg10 VP23-BAP KO and His KO 28.09.2010.png

After gel extraction has been performed, the 2µL of each ligated plasmids were transformed into BL-21 cells.

Test digestion: ViralBricks in pSB1C3_CMV_VP123_capins

Investigator: Achim

We digested preps of all our 453 Inserts with BamHI & SspI and all our 587 Inserts with SalI and PvuII. That way we get bands of ~50 bp difference between our loop inserts and the wt loop region. (Eg. 453 BAP: 455 with insert, 396 without insert.)

Nomenclature as in previous VB assays.

Clone 11.2 is missing , I forgot to inoculate it.

P580 (pSB1C3_CMV_VP123_capins)

The framed samples were midiprepped and will be used for transfection

Sequencing result of pSB1C3_email and pBAD_Affibody_middlelinker_EGFP_His

Investigator: Jessica
1. pSB1C3_email:

2. pBAD_Affibody_middlelinker_EGFP_His:

Preparation of PBS Buffer and PBS Buffer with Imidazole

Investigator: Jessica

The following protocol was used:

dissolve the following in 800ml ddH₂O:
- 8g of NaCl
- 0.2g of KCl
- 1.44g of Na₂HP0₄ (1.69 because of the crystal water in the reagent)
- 0.24 g of KH₂PO₄
adjust to pH 7.4
adjust to 1000ml
steril filtrate the solution

dissolve the following in 180ml ddH₂O:
- 6,4g of NaCl
- 0,16g of KCl
- 1,15g of Na₂HP0₄ (1.69 because of the crystal water in the reagent)
- 0,19 g of KH₂PO₄
- 3,4g of Imidazole
adjust to pH 7.4
adjust to 200ml
steril filtrate the solution

ViralBrick Sequencing results: pSB1C3_587_KO_Z34C and pSB1C3_587_KO_Z34C_Spacer

Investigator: Achim

Sequencing showed that the PCR reaction we designed to remove the mutations in the z34c insert were successful! Both pSB1C3_587_KO_Z34C and pSB1C3_587_KO_Z34C_Spacer are correct. We hadn't sent the 587_Z34C for sequencing because the colony PCR hadn't shown any bands. But because this construct is less important for cell culuture, we won't continue working on this construct.

Cloning of Darpin into pCerulean_Vp1up_NLS and pSB1C3

Investigator: Achim

The Darpin needs to be cloned into pSB1C3 for submission to the parts registry as well as into pCerulean for expression.

Darpin ( cut with NgOMIV & SpeI
Vectors cut with AgeI & SpeI

- -> Results in fusion protein

Cloning of pSB1C3_001_CMV and pSB1C3_001_Vp2/3_HSPG-Ko_CMV_ZEGFR:1907

Investigator: Anissa
Comment: By working with three-fragment-ligation, CMV and ZEGFR:1907 will each be cut out of pSB1C3, will be ligated together and into the vector pSB1C3_001_Vp2/3_HSPG-Ko. Additionally, CMV will be cloned freom pSB1C3 into pSB1C3_001

Vector: name:pSB1C3_001_Vp2/3_HSPG-Ko P613 c=273,6 ng/µl
Vector: name: pSB1C3_001_bla P320 c=408 ng/µl
Insert: name: pSB1C3_CMV P146 c=155,6 ng/µl
Insert: name: pSB1C3_ZEGFR:1907 P268 c=162,5 ng/µl
new vector name: pSB1C3_001_CMV
new vector name: pSB1C3_001_Vp2/3_HSPG-Ko_CMV_ZEGFR:1907
buffer used: 4

components	pSB1C3_CMV /µl	pSB1C3_ZEGFR:1907 /µl	volume of pSB1C3_001_bla /µl	volume of pSB1C3_001_Vp2/3_HSPG-Ko/µl
DNA	12,7	12,3	3,6	5,5
BSA (10x)	2	2	1,5	1,5
Buffer 4 (10x)	2	2	1,5	1,5
Enzyme SpeI	1	-	1	-
Enzyme EcoRI	1	-	1	1
Enzyme XbaI	-	1	-	-
Enzyme AgeI	-	1	-	-
Enzyme NgoMIV	-	-	-	1
H2O	1,3	1,7	6,4	4,5
Total volume (e.g. 15,20,25,30 µl)	20	20	15	15

0,5 g Agarose, 55 ml TAE (1%), 1,5 µl GELRED , at 115Volt

	Marker	P146, 20µl	P268, 20µl	P320, 20µl	P613, 20µl
Fragment size	-	650 bp	170 bp	2100 bp	4000 bp

Gel extraction:

	pSB1C3_CMV (p146)	pSB1C3_ZEGFR:1907 (p268)	pSB1C3_001_bla (p320)	pSB1C3_001_Vp2/3_HSPG-Ko (p613)
DNA-concentration [ng/µl]	28,2	13,2	22,1	43,2

T4 Ligation pSB1C3_001_CMV:
Volume vector p320: 4,63 µl
Volume insert p146: 3,37 µl

T4 Ligation pSB1C3_001_Vp2/3_HSPG-Ko_CMV_ZEGFR:1907:
Volume vector p613: 2,9 µl
Volume insert p268: 3 µl
Volume insert p146: 3 µl

Transformation:
Was performed in BL21 according the standard protocol

CD assembly with new suffix primer

Investigator: Kira

PCR program:

components	volume in µl	volume in µl
5x Phusion HF buffer	10	10
10 mM dNTP mix	1	1
0158 primer_for (1:10 dilution)	2,5	2,5
0159 primer_rev (1:10 dilution)	2,5	2,5
DNA template (1:100)	0,5	0,5
DMSO	0	0.5
Phusion polymerase	0,5	0,5
H₂O	33	32,5
Total volume (e.g. 50 µl)	50	50

Cycles	Temperature	Time
	98°C	1
10x	98°C	15"
	60°C	25"
	72°C	40"
20x	98°C	15"
	65°C	25"
	72°C	40"
1x	72°C	5'
Hold 4°C

no PCR bands are visible on the gel..--> PCR reaction failed.

test digestion of all CD constructs

Investigator: Kira

Comment: Because the PCR failed also with new suffix primer, we decided to check if the DNA samples are ok. 3 different CD samples were used as DNA samples.
1_original CD with iGEM binding sites p(223)
2_CD with SDM of PstI
3_CD with SDM of PstI and NgoMIV (p290)

components	volume in µl
DNA	3
BSA 10x	2,0
Buffer 4	2,0
PstI-HF	0,5
NgoMIV	1,0
H₂O	11,5
Total volume (e.g. 20 µl)	20

Cloning of pSB1C3_Affibody_middlelinker_EGFP_His

Investigator: Jessica
Comment: There was a mistake in cloning pSB1C3_Affibody_middlelinker_EGFP_His so there is just pSB1C3_EGFP_His. in this plasmid will be cloned Affibody_middlelinker_EGFP_His

Vector: name: pSB1C3_EGFP_His P565
Insert: name: pBAD_Affibody_middlelinker_EGFP_His P596
new vector name: pSb1C3_ZEGFR:1907_middlelinker_EGFP_His P
buffer used: 4
DNA concentration (vector): 252,7 ng/µl; DNA concentration (insert): 101,4 µg/µl

components	volume of pBAD /µl	volume of pSB1C3 /µl
DNA	15	4
BSA (10x)	2	2
Buffer 4 (10x)	2	2
Enzyme XbaI	0,8	0,8
Enzyme AgeI	0,8	0,8
H2O	-	10,4
Total volume (e.g. 15,20,25,30 µl)	20,6	20

0,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 120 Volt

	Marker	P565, 20µl	P596, 20µl
Sample
Fragment size		2100 bp	1000 bp

Gel extraction:

	pSB1C3	Affibody_middlelinker_EFGP_His
DNA-concentration [ng/µl]	17,5	14,2

T4 Ligation:
Volume vector: 2,9 µl
Volume insert: 5,1 µl

Transformation:

BL21 cells were used

Sequencing analysis of pSB1C3_001_RC_IRCK, pSB1C3_001_RC_IRCK_VP1-ko_P5tataless and pSB1C3_001_RC_IRCK_VP2-ko_P5tataless

Investigator: Stefan

Because all these constructs were cloned via PCR out of the pAAV vector, a complete sequencing was performed:

P548 pSB1C3_001_RC_InsRepCap_KpnIback_VP1-ko_P5tataless clone 1:
Sequence could be verified, can be used for further cloning steps!

P568 pSB1C3_001_RC_InsRepCap_KpnIback_VP2-KO_P5tataless clone 2:
Sequence could be verified, can be used for further cloning steps!

P594 pSB1C3_001_RC_InsRepCap_KpnIback_RFC10 clone 1:
Sequence could be verified, can be used for further cloning steps!

Cloning of HSPG_KO_empty into pSB1C3_001_RC_IRCK_VP1-ko_P5tataless and pSB1C3_001_RC_IRCK_VP2-ko_P5tataless

Investigator: Stefan

Vector name:

pSB1C3_001_RC_IRCK_VP1-ko_P5tataless (P548)
pSB1C3_001_RC_IRCK_VP1-ko_P5tataless (P568)

Insert name:

VB:pSB1C3_001_KO_empty(P611)

components	volume of P548 /µl	volume of P568 /µl	volume of P611 /µl
DNA	3,5	3,5	16
BSA (10x)	2	2	3
Buffer 4 (10x)	2	2	3
Enzyme BamHI	1	1	1
Enzyme PvuII	1	1	1
H2O	10,5	10,5	6
Total volume (e.g. 15,20,25,30 µl)	20	20	30

Gel:

for vector:
0,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 115 Volt

for insert:

1 g Agarose, 50 ml TAE (2%), 3 µl GELRED , at 105 Volt

Gel extraction:
Was performed according to protocol.

T4 Ligation:

VP1-ko:

Volume VP1-ko: 5,57 µl
Volume insert: 2,43 µl

VP2-ko

Volume VP2-ko: 5,04 µl
Volume insert: 2,96 µl

Transformation:
Was performed according to standard protocol using BL21 cells.

Cloning of 587_KO_Z34C and 587_KO_Z34C_Spacer into pSB1C3_001_CMV_VP123_capins

Investigator: Anna

Comment: Todays sequencing results of 587_KO_Z34C and 587_KO_Z34C_Spacer looked well, so they will be cloned into pSB1C3_CMV_VP123_capins. Finally produced ViralBricks:

media:Freiburg10_Production of ViralBricks_End version.pdf

Vector name: pSB1C3_CMV_VP123_capins P580
Insert name:

1. pSB1C3_587_KO_Z34C P599
2. pSB1C3_587_KO_Z34C_Spacer P600

buffer used: 4

DNA concentration (P580): 377,29 ng/µl;
DNA concentration (P599): 102,5 µg/µl
DNA concentration (P600): 90,4 µg/µl

components	volume of P580 /µl	volume of P599 /µl	volume of P600 /µl
DNA	2,7	14,7	16,7
BSA (10x)	2,5	2,5	2,5
Buffer 4 (10x)	2,5	2,5	2,5
Enzyme BamHI	1	1	1
Enzyme PvuII	1	1	1
H2O	15,3	3,3	1,3
Total volume (e.g. 15,20,25,30 µl)	25	25	25

0,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 120 Volt

	Marker, 4 µl	P580	2: P599	3: P600
Construct		pSB1C3_CMV_VP123_cut	587_KO_Z34C	587_KO_Z34C_Spacer
Fragment size		5000 bp	194 bp	209 bp

Gel extraction:
Was performed following the standard protocol.
DNA-concentrations [ng/µl]:

c(vector)= 18,88
c(587_KO_Z34C)= 9,74
c(587_KO_Z34C_Spacer)= 1,72

T4 Ligation:

587_KO_Z34C:
Volume vector: 1,5 µl
Volume insert: 6,5 µl

587_KO_Z34C_Spacer:
Volume vector: 4,6 µl
Volume insert: 3,4 µl

Trafo:
Was performed following the standard protocol using BL21 cells.

Mini-Prep and Test-digestion of VP1 insertion and VP2 fusion HSPG-KO approaches

Investigator: Hanna

Comments: Yesterday, 2 clones of each construct were picked. Today mini-prep and test digestion will be performed of one of each approach - the other clones will be spinned down and stored at -20°C - waiting for test digestion and sequencing results.

Mini-Prep was performed, following the standard protocol.

New plasmid names:
P617: pCerulean_CFP_MiddleLinker_VP2/3_HSPG-KO
P618: pCerulean_ZEGFR:1907_MiddleLinker_VP2/3_HSPG-KO
P619: pCerulean_ZEGFR:1907_SEG_VP2/3_HSPG-KO
P620: pCerulean_ZEGFR:1907_ShortLinker_VP2/3_HSPG-KO
P621: pCerulean_ZEGFR:1907_LongLinker_VP2/3_HSPG-KO
P622: pCerulean_6xHis_MiddleLinker_VP2/3_HSPG-KO
P623: pCerulean_VP1up_NLS_ZEGFR:1907_VP2/3_HSPG-KO
P624: pCerulean_VP1up_NLS_6xHis_VP2/3_HSPG-KO
P625: pCerulean_VP1up_NLS_mVenus_VP2/3_HSPG-KO

TEST DIGESTION:
Mastermix:

BSA (10x): 10 µL
Buffer 4: 10 µL
EcoRI: 5 µL
PstI: 5 µL
H₂O: 37 µL

DNA: 3.3 µL + 6.7 µL Master Mix.

Conclusion: Test digestion looked well - except of P618: There is an additional band visible, which can't be correlated to any construct.
All samples were sent for sequencing.

134. labday 29.09.2010

CD assembly with new suffix primer

Investigator: Kira

PCR program:

as DNA samples p291 and p292 with and wo DMSO were used.

components	volume in µl	volume in µl
5x Phusion HF buffer	10	10
10 mM dNTP mix	1	1
0158 primer_for (1:10 dilution)	2,5	2,5
0159 primer_rev (1:10 dilution)	2,5	2,5
DNA template (1:100)	0,5	0,5
DMSO	0	0.5
Phusion polymerase	0,5	0,5
H₂O	33	32,5
Total volume (e.g. 50 µl)	50	50

Cycles	Temperature	Time
	98°C	1
10x	98°C	15"
	60°C	25"
	72°C	40"
20x	98°C	15"
	65°C	25"
	72°C	40"
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 (10x)	2 µl
Buffer no. 4 (10x)	2,0 µl
Enzyme 1 XbaI	1,0 µl
Enzyme 2 AgeI	1,5 µl
H₂O	7,5 µl
Total volume	20

incubation @ 37 C for approx. 2 h

1% agarose gel

Digestion of PCR product:

Components	PCR product Volume/µL
DNA	30,0 µl
BSA (100x)	0,4 µl
Buffer no. 4	4,0 µl
Enzyme 1 XbaI	1,5 µl
Enzyme 2 AgeI	2,0 µl
H₂O	2,1 µl
Total volume	40

incubation @ 37 C for approx. 2 h

ligation with T4 ligase:
c(insert)= 31,35 ng/ul
c(vector)= 10,45 ng/ul
8ul DNA mix = insert 3 ul + vector 5 ul
T4 ligase 1 ul
T4 buffer 1 ul

Transformation: Anna

Miniprep of serveral constructs

Investigator: Stefan

Glycerol stocks were prepared:

B516 = pSB1C3_001_RC_ICRK_P5tataless_RFC10 clone 1
B517 = pSB1C3_pTAV (P5)
B518 = pSB1C3_001_RC_ICRK_P5tataless_RFC10 clone 2

Mini-Prep was performed according to the standard protocol

P628 = pSB1C3_001_RC_ICRK_P5tataless_RFC10 clone 1
P629 = pSB1C3_pTAV (P5)
P630 = pSB1C3_001_RC_ICRK_P5tataless_RFC10 clone 2

Test digestion:

Components	Volume P628 + P630 /µl
DNA	3
BSA	1
Buffer 4 (10x)	1
Enzyme I	0,4
Enzyme II	0,4
H₂O	4,2
Total volume	10

Comment:First test digestion using XmaI and SpeI did not work out, thererfore, two different approaches using MngBI/PstI and SnaBI and PstI were performed. This verified successful cloning of P5tataless into the target vector.

Sent for sequencing:

pSB1C3_001_RC_ICRK_P5tataless_RFC10 clone 1 (P628) was sent for sequencing using VR2 primer.

mGMK_TK30 approaches

Investigator: Bea

Comment: Since we are still waiting for the TK30 gene ordered at Mr.Gene we decided to take another road to produce a BioBrick compatible thymidine kinase gene. Therefore, we are cloning the mGMK_TK30 fusion construct into the pSB1C3 and after removing the PstI site (see next topic) it is ready for submitting it to the parts registry. Additionally, we are fusing the mGMK_TK30 to the composite part pSB1C3-leftITR_PROMOTER_betaglobin for testing it in cell culture with pur final super construct.

Digestion of the constructs:

P51.2 = pSB1C3_CFP
P81 = pAAV_RFC25_mGMK_TK30
P434 = pSB1C3_leftITR_CMV_betaglobin
P437 = pSB1C3_leftITR_phTERT_betaglobin

Components	v_P51.2 /µL	v_{P81 upstream}/µL	v_P81 /µL	v_P434/µL	v_P437/µL
DNA	5	5	10	4,5	4,5
BSA (10x)	2	2	2	2	2
Buffer no. 4 (10x)	2	2	2	2	2
Enzyme 1	EcoRI	SpeI	SpeI 1	-	-
Enzyme 2	SpeI	XbaI	EcoRI	SpeI	SpeI
H₂O	9	9	4	10,5	10,5
Total volume	20	20	20	20	20

Overview cloning plan:

Loading plan of a 0,8% agarose gel:

M    P51.2    P81 (digested with E+S)    P81 (digested with X+S)    P434    P437

Expected sizes of the digested products are:

pAAV_RFC25_mGMK_TK30= 4626, 1717bp
pAAV_RFC25_mGMK_TK30= 4626, 1717bp
pSB1C3_CFP = 2052, 756bp
pSB1C3_leftITR_CMV_betaglobin= 5094b
pSB1C3_leftITR_phTERT_betaglobin= 5094b

Results:

Freiburg10 mGMK TK30 several approaches 29.09.2010.png

After Gel extraction have been performed the ligation was conducetd:

Freiburg10 mGMK TK30 ligation 29.09.2010.png

Design of mutagenesis primers for deletion of PstI in mGMK_TK30

Investigator: Bea

Comment: Since we are still waiting for the TK30 gene ordered at Mr.Gene we decided to take another road to produce a BioBrick compatible thymidine kinase gene. Therefore, new primers were designed in order to remove the PstI restriction sites within the TK30 gene. The primers will be ordered tomorrow.

Freiburg10 PrimerDesign TK30 SDM PstI 29.09.2010.PNG

Cloning of Darpin into pCerulean_Vp1up_NLS and pSB1C3 Part Two

Investigator: Achim

I accidentally plated yesterdays trafo with the wrong antibiotics and I had to digest pSB1C3 again anyway, so I prepared a new digestion of both vectors with Age & Spe.

After watching the gel picture I realized I had digested pSB1C3 with the wrong enzymes. I should have used NgOMIV and Spe in order to cut out BLA.

pCerulean_Vp1up_NLS was ligated with yesterdays Darpin fragment and plated on Ampicillin, the pSB1C3_BLA construct will be cloned correctly tomorrow

Cloning of pGGTBT7_Affibody_middlelinker_EGFP_His

Investigator: Jessica
Comment: pBAD is not really working, so we test another expression-plasmid

Vector: name: pGGTBT7_MVenus P627
Insert: name: pBAD_Affibody_middlelinker_EGFP_His 596prepared yesterday
new vector name: pGGTBT7_ZEGFR:1907_middlelinker_EGFP_His P
buffer used: 4
DNA concentration (vector): 144,1 ng/µl; DNA concentration (insert): 101,4 µg/µl

components	volume of pBAD /µl
DNA	10
BSA (10x)	2
Buffer 4 (10x)	2
Enzyme XbaI	0,8
Enzyme AgeI	0,8
H2O	4,4
Total volume (e.g. 15,20,25,30 µl)	20

0,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 120 Volt

Fragment size		5200 bp	730 bp

Gel extraction:

	pGGTBT7	Affibody_middlelinker_EFGP_His
DNA-concentration [ng/µl]	20,79	7,84

T4 Ligation:
Volume vector: 3,2 µl
Volume insert: 4,8 µl

Transformation:

BL21 DE3 R2L(Kana+Cm), BL21 DE3(Kana), BL21DE3 R2(Kana+Cm) cells were used

Cloning of CMV promotor and Affibody into pSB1C3_001_VP2/3_capins and pSB1C3_001_VP2/3_HSPG_KO

Investigator: Anna

Comment: Cloning of CMV promotor and Affibody into pSB1C3_001_VP2/3_HSPG_KO was repeated, because it was not clear if the first attempt worked.

Vector name:

1. pSB1C3_001_VP2/3_capins P514: 318,9 ng/µl
2. pSB1C3_001_VP2/3_HSPG_KO P613: 273,6 ng/µl

Insert name:

1. pSB1C3_CMV P146: 155,6 ng/µl
2. pSB1C3_ZEGFR:1907 P248: 146,5 ng/µl

buffer used: 4

components	volume of P514 /µl	volume of P613 /µl	volume of P146 /µl	volume of P248 /µl
DNA	3,1	3,7	12,8	13,7
BSA (10x)	2,0	2,0	2,0	2,0
Buffer 4 (10x)	2,0	2,0	2,0	2,0
Enzyme I	EcoRI 1	EcoRI 1	XbaI 1	SpeI 1
Enzyme II	NgoMIV 1	NgoMIV 1	AgeI 1	EcoRI 1
H2O	10,9	10,3	1,2	0,3
Total volume (e.g. 15,20,25,30 µl)	20	20	20	20

0,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 120 Volt

	Marker, 4 µl	Vector 1: pSB1C3_001_VP2/3_capins	Vector 2: pSB1C3_001_VP2/3_HSPG_KO	CMV	Affibody
Fragment size		4000 bp	4000 bp	650 bp	170 bp

Gel extraction:
Was performed following the standard protocol.
DNA-concentrations [ng/µl]:

c (pSB1C3_001_VP2/3_capins) = 40.9
c (pSB1C3_001_VP2/3_HSPG_KO)= 51.94
c (CMV)= 12.67
c (Affibody)= 14.44

T4 Ligation:

Vector 1:

Volume vector: 2,8 µl
Volume Affibody: 2,0 µl
Volume CMV: 3,2 µl

Vector 2:

Volume vector: 2,5 µl
Volume Affibody: 2,0 µl
Volume CMV: 3,5 µl

Trafo:
Was performed following the standard protocol using BL21 cells.

Cloning of CFP into pSB1C3_lITR_phTERT_beta-globin

Investigator: Anissa

Vector name:

pSB1C3_lITR_phTERT_beta-globin P514: 333,46 ng/µl

Insert name:

pSB1C3_CFP P146: 151,1 ng/µl

buffer used: 4

components	volume of P51.2 /µl	volume of P437 /µl
DNA	13,2	4,5
BSA (10x)	2,0	1,5
Buffer 4 (10x)	2,0	1,5
Enzyme I	XbaI 1	SpeI 1
Enzyme II	PstI 1	PstI 1
H2O	0,8	5,5
Total volume (e.g. 15,20,25,30 µl)	20	15

0,5 g Agarose, 50 ml TAE (1%), 1,5 µl GELRED , at 115 Volt

	Marker, 4 µl	Vector	Insert
Fragment size		3180 bp	750 bp

Gel extraction:
Was performed following the standard protocol.
DNA-concentrations [ng/µl]:

c (pSB1C3_CFP) = 11,6
c (pSB1C3_lITR_phTERT_beta-globin)= 24,8

T4 Ligation:

Volume vector: 3,2 µl
Volume insert: 4,8 µl

Trafo:
Was performed following the standard protocol using BL21 cells.

Sequencing results: VP1 insertion and VP2 fusion: Fusion of VP2/3_HSPG-KO

Investigator: Hanna

Sample gallery
pCerulean_CFP_MiddleLinker_ VP2/3_HSPG-KO (P617)	pCerulean_Z_EGFR:1907_MiddleLinker_ VP2/3_HSPG-KO (P618)
pCerulean_Z_EGFR:1907_SEG_ VP2/3_HSPG-KO (P619)	pCerulean_Z_EGFR:1907_ShortLinker_ VP2/3_HSPG-KO (P620)
pCerulean_Z_EGFR:1907_LongLinker_ VP2/3_HSPG-KO (P621)	pCerulean_6xHis</sub>_MiddleLinker_ VP2/3_HSPG-KO (P622)
pCerulean__VP1up_NLS_Z_EGFR:1907_ VP2/3_HSPG-KO (P623)	pCerulean_VP1up_NLS_6xHis_ VP2/3_HSPG-KO (P624)
pCerulean_VP1up_NLS_mVenus_ VP2/3_HSPG-KO (P625)

Conclusion: Except of pCerulean_Z_EGFR:1907_MiddleLinker_ VP2/3_HSPG-KO (P618), all sequencing results looked well. This means: The VP2/3-HSPG-KO motif was cloned successfully to the VP2-Fusion and VP1-Insertion approaches and are ready to be tested in cell culture via qPCR and ELISA. --> Co-transfection with pSB1C3_001_RC_iRCK_VP1or2-KO_HSPG-KO + pHelper + pSB1C3_GOI.

In addition to that, clone 2 of pCerulean_Z_EGFR:1907_MiddleLinker_ VP2/3_HSPG-KO will be preped and test digested tomorrow.

Cloning of HSPG_KO_empty into pSB1C3_001_RC_IRCK_P5tataless

Investigator: Stefan

Vector name:

pSB1C3_001_RC_IRCK_P5tataless cl1 (P628)
pSB1C3_001_RC_IRCK_P5tataless cl2 (P630)

Insert name:

VB:pSB1C3_001_KO_empty(P611)

components	volume of P628 /µl	volume of P630 /µl	volume of P611 /µl
DNA	3,5	3,5	16
BSA (10x)	2	2	3
Buffer 4 (10x)	2	2	3
Enzyme BamHI	1	1	1
Enzyme PvuII	1	1	1
H2O	10,5	10,5	6
Total volume (e.g. 15,20,25,30 µl)	20	20	30

Gel:
for vector:
0,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 110 Volt

for insert:
1 g Agarose, 50 ml TAE (2%), 3 µl GELRED , at 110 Volt

Gel extraction:
Was performed according to protocol.

T4 Ligation:

Volume vector P628: 7,11 µl
Volume insert: 0,89 µl

Volume vector P630: 7,33 µl
Volume insert: 0,67 µl

Transformation:
Was performed according to standard protocol using BL21 cells.

Mass Midi-Prep II

Investigator: Chris W.

Midi-Prep of:

453_BAP =P631
587_BAP =P632
587_KO_BAP =P633
453_RGD =P634
587_RGD =P635
587_KO_RGD =P636
453_HIS =P637
587_HIS =P638
587_KO_HIS =P639
587_KO_empty =P640
453_Z34C =P641
pSB1C3_001_RC_IRCK_VP1-ko_P5tataless =P642 =B463
pSB1C3_001_RC_IRCK_VP2-ko_P5tataless =P643 =B470

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

plasmid-no.	P631	P632	P633	P634	P635	P636	P637	P638	P639	P640	P641	P642	P643
concentration (ng/µl)	4758,69	448,12	3243,97	2231,44	1401,68	3289,15	3441,22	3058,92	4425,05	2339,06	4377,05	5045,55	5201,73

135. labday 30.09.2010

picking CD clones

Investigator: Kira The agaro plate contained many clones, 4 of them were picked and inoculated into media

ViralBricks BAP-ko and His-ko in VP23

Investigator: Bea

Comment: In order to verify the insertion of the ViralBricks BAP-ko and His-ko into the VP23 construct we digested the produced constructs with SalI and BamHI (both HF) and loaded it on a 1%a agarose gel. The constructs were used for creating the final super constructs (yay). Sequencing will verify if we subcloned the ViralBrick truly/seriously into the plasmids.

Digestion of the constructs:

P660 = pSB1C3_001_VP2/3_HSPG-ko_587_BAP
P661 = pSB1C3_001_VP2/3_HSPG-ko_587_BAP

Expected size: 464bp

P662 = pSB1C3_001_VP2/3_HSPG-ko_587_His
P663 = pSB1C3_001_VP2/3_HSPG-ko_587_His

Expected size: 437bp

P525 = pSB1C3_001_VP2/3_capins

Expected size: 404bp

Freiburg10 Testdigestion BiralBricks VP23 29.09.10.png

Results:
The detected bands correspond to the expected sizes, but we cannot distinguish between the exact sizes because they are too similar. Therefore we sent P660 and P663 for sequencing in order to confirm if the ViralBricks have been successfully subcloned in the pSB1c3_VP2/3 construct.

Cloning of Darpin into pCerulean_Vp1up_NLS and pSB1C3 Part Three

Investigator: Achim

Clones of the pCerulean_Vp1up_NLS_Darpin construct were picked and will be prepped tonight.

pSB1C3_001_BLA (P320) and pMA_Darpin (P614) were digested with NgOMIV and SpeI. Bands were cut out accordingly, ligated with T4 ligase and plated on Chloramphenicol.

Test digestion of pCerulean_Z_EGFR:1907_MiddleLinker_VP2/3_HSPG-KO clone 2

Investigator: Hanna

Comment: Yesterday's sequencing results revealed, that VP2/3_HSPG-KO was successfully cloned to the VP2 fusion and VP1 insertion approaches, except of pCerulean_Z_EGFR:1907_MiddleLinker_VP2/3_HSPG-KO clone 2. The chromatogram showed that fusion worked, but there was a kind of contamination in the sample - already visible in the test digestion.

DNA = 2 µL
BSA (10x) = 1 µL
Buffer 4 = 1 µl
EcoRI = 0.5 µL
PstI = 0.5 µL
H₂0 = 5 µL

Incubation time = 45 minutes.
0.9 % Agarose gel.

Test digestion looked well. Sample was sent for sequencing.

Cloning VP2/3_Capins and VP2/3_HSPG-KO downstream of Middle Linker

Investigator: Hanna

Comment: Besides the Affibody we also want to test and characterize the DARPin for its binding properties referring to the VP2 fusion and VP1 insertion. Therefore some preliminary cloning steps have to be performed. Today the VP2/3_insCap and VP2/3_HSPG-KO sequence will be cloned downstream of the Middle Linker for the VP2 fusion.

Practical Cloning:

- Vector: pGA14_MiddleLinker (P301)
- Insert: pSB1C3_VP2/3_insCap (P525) and pSB1C3_001_VP2/3_HSPG-KO (P613)
new vector name: pGA14_MiddleLinker_VP2/3_insCap and pGA14_MiddleLinker_VP2/3_HSPG-KO
buffer used: 4 ; Restriction-enzymes used: PstI, AgeI/NgoMIV

Digestion

components	volume of P301 /µl	volume of P525 /µl	volume of P613 /µl
DNA	5	7.6	5.5
BSA (10x)	2	2	2
Buffer 4 (10x)	2	2	2
PstI	1	1	1
AgeI	1	-	-
NgoMIV	-	1	1
McsI	0.5	0.5	0.5
H₂O	9	6.4	8.5
Total volume	20	20	20

Comment: After 30 minutes of digestion I remembered that it would be adventageous to digest the plasmid backbone of the VP2/3 constructs. Therefore 0.5 µL of McsI was added to each sample - fortunately McsI does not have any restriction sites in the pGA14_MiddleLinker to which it was also added by mistake.

Incubation: 20 minutes + 2 hours.

Agarose-Gel:

0.5 g Agarose, 50 mL TAE (1 %), 3 µL GELRED, at 10 Volt, running time: 45 minutes

Sample	Sample/µl]	Loading dye (6x)/µl	Expected size 1	Expected size 2	Expected size 3
P301	20 µl	4 µl	~ 2450 bp
P525	20 µl	4 µl	1951 bp	738 bp	1324bp
P613	20 µl	4 µl	1951 bp	738 bp	1324bp

Marker: GeneRuler ladder mix

	Marker /µl	Sample P301 /µl	Sample P525 /µl	Sample P613 /µl
Lane	4.5	24	24	24

Gel extraction

Gel measurement:

Sample	Weight	Concentration
P301	250 mg	38.41
P525	270 mg	18.21
P613	300 mg	21.55

Ligation

Construct	Vector (µl)	Insert (µl)	T4 Ligase Buffer (µl)	T4 Ligase (µl)
pGA14_MiddleLinker_VP2/3_insCap	1.32	6.68	1	1
pGA14_MiddleLinker_VP2/3_HSPG-KO	1.52	6.48	1	1

Miniprep of serveral constructs

Investigator: Jessica

Glycerol stocks were prepared:

B527 pSB1C3_001_CMV_VP2/3_587-KO_Z34C_spacer clone3
B528 pSB1C3_001_CMV_VP123_587-KO_Z34C clone1
B529 pSB1C3_001_CMV_VP123_587-KO_Z34C clone2
B530 pSB1C3_001_CMV_VP123_587-KO_Z34C clone3
B531 pSB1C3_oo1_CMV clone1
B532 pSB1C3_oo1_CMV clone2
B533 pSB1C3_001_CMV_ZEGFR:1907_VP2/3_HSPG-KO clone1
B534 pSB1C3_001_CMV_ZEGFR:1907_VP2/3_HSPG-KO clone2
B535 pSB1C3_001_VP2/3_ins_HSPG-KO_CMV_ZEGFR:1907 clone 1
B536 pSB1C3_001_VP2/3_ins_HSPG-KO_CMV_ZEGFR:1907 clone 2
B537 pBS1C3_001_VP2/3_587_BAP_HSPG-KO clone1
B538 pBS1C3_001_VP2/3_587_BAP_HSPG-KO clone2
B539 pBS1C3_VP2/3_capins_His clone1
B540 pBS1C3_VP2/3_capins_His clone2
B541 pSB1C3_ZEGFR:1907 _middlelinker_EGFP_His clone1
B542 pSB1C3_ZEGFR:1907 _middlelinker_EGFP_His clone2

Mini-Prep was performed according to the standard protocol

P644 pSB1C3_001_RC_IRCK_VP1-ko_HSPG-ko_P5tataless cl1 c= 151,0 ng/µl
P645 pSB1C3_001_RC_IRCK_VP1-ko_HSPG-ko_P5tataless cl2 c= 115,8 ng/µl
P646 pSB1C3_001_RC_IRCK_VP2-ko_HSPG-ko_P5tataless cl1 c= 173,1 ng/µl
P647 pSB1C3_001_RC_IRCK_VP2-ko_HSPG-ko_P5tataless cl2 c= 119,9 ng/µl
P648 pSB1C3_001_CMV_VP123_587-KO_Z34C_spacer clone1 c= 226,8 ng/µl
P649 pSB1C3_001_CMV_VP123_587-KO_Z34C_spacer clone2 c= 290,3 ng/µl
P650 pSB1C3_001_CMV_VP123_587-KO_Z34C_spacer clone3 c= 284,2 ng/µl
P651 pSB1C3_001_CMV_VP123_587-KO_Z34C clone1 c= 283,8 ng/µl
P652 pSB1C3_001_CMV_VP123_587-KO_Z34C clone2 c= 290,5 ng/µl
P653 pSB1C3_001_CMV_VP123_587-KO_Z34C clone3 c= 251,7 ng/µl
P654 pSB1C3_oo1_CMV clone1 c= 199,5 ng/µl
P655 pSB1C3_oo1_CMV clone2 c= 192,7 ng/µl
P656 pSB1C3_001_CMV_ZEGFR:1907_VP2/3_HSPG-KO clone1 c= 200,3 ng/µl
P657 pSB1C3_001_CMV_ZEGFR:1907_VP2/3_HSPG-KO clone2 c= 325,0 ng/µl
P658 pSB1C3_001_CMV_ZEGFR:1907_VP2/3_HSPG-KO clone3 c= 222,9 ng/µl
P659 pSB1C3_001_CMV_ZEGFR:1907_VP2/3_HSPG-KO clone4 c= 201,3 ng/µl
P660 pBS1C3_001_VP2/3_587_BAP_HSPG-KO clone1 c= 267,1 ng/µl
P661 pBS1C3_001_VP2/3_587_BAP_HSPG-KO clone2 c= 193,1 ng/µl
P662 pBS1C3_VP2/3_capins_His clone1 c= 209,1 ng/µl
P663 pBS1C3_VP2/3_capins_His clone2 c= 252,5 ng/µl
P664 pSB1C3_ZEGFR:1907 _middlelinker_EGFP_His clone1 c= 185,7 ng/µl
P665 pSB1C3_ZEGFR:1907 _middlelinker_EGFP_His clone2 c= 192,0 ng/µl
P666 pSB1C3_CFP c= 212,7 ng/µl

Test digestion of pSB1C3_ZEGFR:1907 _middlelinker_EGFP_His and mCherry iGEM 2008

Investigator: Jessica

components	volume of P664 pSB1C3_ZEGFR:1907 _middlelinker_EGFP_His /µl	volume of P665 pSB1C3_ZEGFR:1907 _middlelinker_EGFP_His /µl	volume of P626 mCherry /µl
DNA	1,5	1,5	1,5
BSA (10x)	1	1	1
Buffer 4 (10x)	1	1	1
XbaI	0,4	0,4	0,4
AgeI	0,4	0,4	0,4
H₂O	5,7	5,7	5,7
Total volume	10	10	10

Sample gallery

Test digestion of pSB1C3_001_CMV_affibody_HSPG_KO and pSB1C3_001_CMV_VP123_587_KO_Z34C

Investigator: Anna

Comment: 587_KO_Z34C and 587_KO_Z34C_Spacer were cloned into pSB1C3_001_CMV_VP123 as already done with the other 453 and 587 constructs (see test digestion from labday 28.09.) The test digestion looks well, nevertheless one sample out of these constructs should be sent for sequencing.

components	volume of pSB1C3_001_CMV_affibody_HSPG_KO /µl	volume of pSB1C3_001_CMV_VP123_587_KO_Z34C /µl	volume of pSB1C3_001_CMV_VP123_587_KO_Z34C_Spacer /µl
DNA	3	3	3
BSA (10x)	1,5	1,5	1,5
Buffer 4 (10x)	1,5	1,5	1,5
EnzymeI	SspI 0,3	SalI 0,3	SalI 0,3
EnzymeII	EcoRI 0,3	PvuII 0,3	PvuII 0,3
H₂O	4,8	4,8	4,8
Total volume	15	15	15

Sample	1	2	3	4	5	6	7
Construct	587_KO_Z34C	587_KO_Z34C	587_KO_Z34C	587_KO_Z34C_Spacer	587_KO_Z34C_Spacer	587_KO_Z34C_Spacer	p580
Clone	1	2	3	1	2	3

Sample	8	9	10	11	12
Construct	p613	CMV_EGFR:1907	CMV_EGFR:1907	CMV_EGFR:1907	CMV_EGFR:1907
Clone		1	2	3	4

Midiprep of pSB1C3_001_CMV_VP1/2/3_capins_587bla and pSB1C3_001_RC_IRCK_P5tataless clone1

Investigators: Chris W.

Midi-Preps of:
pSB1C3_001_CMV_VP1/2/3_capins_587bla =P667
pSB1C3_001_RC_IRCK_P5tataless clone1 =P668

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

plasmid-no.	P667	P668
concentration (ng/µl)	1502,3	991,6

Cloning of VP2/3_BAP_HSPG-KO and VP2/3_His_HSPG-KO into pCerulean_Zegfr:1907_Middlelinker and VP2/3_His_HSPG-KO into pCerulean_VP1up_NLS_mVenus

Investigator: Stefan

Vector name:

pCerulean_Zegfr:1907_Middlelinker (P408)
pCerulean_VP1up_NLS_mVenus (P426)

Insert name:

pBS1C3_001_VP2/3_587_BAP_HSPG-KO clone1 (P660)
pBS1C3_001_VP2/3_587_BAP_HSPG-KO clone2 (P661)
pBS1C3_001_VP2/3_587_His_HSPG-KO clone1 (P662)
pBS1C3_001_VP2/3_587_His_HSPG-KO clone2 (P663)

components	volume for inserts (P660 - P663) /µl	volume of P408 /µl	volume of P426 /µl
DNA	10	3	3
BSA (10x)	3	2	2
Buffer 4 (10x)	3	2	2
Enzyme NgoMIV	1	-	-
Enzyme PstI	1	1	1
Enzyme MscI	1	-	-
Enzyme AgeI	-	1	1
H2O	11	11	11
Total volume (e.g. 15,20,25,30 µl)	30	20	20

Gel:
0,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 115 Volt

Gel extraction:
Was performed according to protocol.

T4 Ligation:

ligation name	408 + 660	408 + 661	408 + 662	408 + 663	426 + 662	426 + 663
volume of vector	3,4	3,05	3,35	2,56	2,74	3,13
volume of insert	4,6	4,95	4,65	5,44	5,26	4,87

Transformation:
Was performed according to standard protocol using BL21 cells.

=> Go to Labjournal October part 1 (labday 136 - 145 )

@@ Line 1: / Line 1: @@
+{{:Team:Freiburg_Bioware/css}}
+{{:Team:Freiburg_Bioware/Head}}
+{{:Team:Freiburg_Bioware/menu_notebook}}
+{{:Team:Freiburg_Bioware/jquery}}
 <!-- Freiburg_bioware -->
+[https://2010.igem.org/Team:Freiburg_Bioware/NoteBook => Back to Notebook overview]<br><br>
 <html>
-<!-- Stylesheed -->
+<div class="box_right">
-<style>
+<left><u1>NoteBook Navigator</u1></left>
+<br>
-#content {
+<ul>
-width: 965px;
+<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/March">March (labday 1)</a></li>
-/*background-color: #3300ee;*/
+<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/April">April (labday 2 - 5)</a></li>
-}
+<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/May">May (labday 6 - 17)</a></li>
+<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/June">June (labday 18 - 45)</a></li>
-#banner_top {
+<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/July">July (labday 46 - 75)</a></li>
-opacity: 1;
+<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/August">August part 1 (labday 76 - 92)</a></li>
-width: 965px;
+<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/August2">August part 2 (labday 93 - 106)</a></li>
-height: 200px;
+<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/September">September part 1 (labday 107 - 123)</a></li>
-margin: 0px 0px 0px 0px;
+<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/September2">September part 2 (labday 124 - 135)</a></li>
-}
+<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/October">October part 1 (labday 136 - 149 )</a></li>
+<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/October2">October part 2 (labday 150 - 166 )</a></li>
-/*Menu and the corresponding buttons*/
+<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/November">November  (labday 167 - 170 )</a></li>
+<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/Cellculture">Cellculture</a></li>
-#menu {
+</ul>
-width: 900px;
-margin: 30px 0px 30px 0px;
-}
-div.menu_button {
-float: left;
-width: 110px;
-}
-div.menu_button a {
-font-weight: bold;
-font-size: 12px;
-/*border: 1px solid black;*/
-text-decoration: none;
-color: #555555;
-background: transparent url(http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/images/7/7e/Freiburg10_Buttongrau100.png) no-repeat scroll center center;
-}
-div.menu_button a:hover {
-/*color: #999999;*/
-background: transparent url(http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/images/9/99/Freiburg10_Buttongruen100.png) no-repeat scroll center center;
-}
-#BHome a {
-padding: 20px 35px 20px 35px;
-margin: 10px 2px 10px 2px;
-}
-#BTeam a {
-padding: 20px 35px 20px 35px;
-margin: 10px 2px 10px 2px;
-}
-#BProject a {
-padding: 20px 30px 20px 30px;
-margin: 10px 2px 10px 2px;
-}
-#BBioBricks a {
-padding: 20px 15px 20px 15px;
-margin: 10px 2px 10px 2px;
-}
-#BNote a {
-padding: 20px 22px 20px 21px;
-margin: 10px 2px 10px 2px;
-}
-#BSponsors a {
-padding: 20px 24px 20px 22px;
-margin: 10px 2px 10px 2px;
-}
-#BSafety a {
-padding: 20px 32px 20px 32px;
-margin: 10px 2px 10px 2px;
-}
-#BModelling a {
-padding: 20px 24px 20px 24px;
-margin: 10px 2px 10px 2px;
-}
-/* Main area */
-div.overall {
-width: 965px;
-margin: 30px 0px 0px 0px;
-}
-#index {
-margin: 100px 0px 0px 50px;
-}
-div.box_right {
-width: 965px;
-height: auto;
-float: left;
-margin: 40px 0px 0px 0px;
-/*border: 1px solid black;*/
-}
-</style>
-<!-- Start stuff you see -->
-<!-- Banner -->
-<img src="http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/images/3/31/Freiburg10_Header_wiki.png" alt="banner" id="banner_top"/>
-<!-- Menu -->
-<center>
-<div id="menu">
-<div class="menu_button" id="BHome"><a href="https://2010.igem.org/Team:Freiburg_Bioware" target="blank">Home</a></div>
-<div class="menu_button" id="BTeam"><a href="https://2010.igem.org/Team:Freiburg_Bioware/Team" target="blank">Team</a></div>
-<div class="menu_button" id="BProject"><a href="https://2010.igem.org/Team:Freiburg_Bioware/Project" target="blank">Project</a></div>
-<div class="menu_button" id="BBioBricks"><a href="https://2010.igem.org/Team:Freiburg_Bioware/BioBricks" target="blank">BioBricks &trade;</a></div>
-<div class="menu_button" id="BNote"><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook" target="blank">Note Book</a></div>
-<div class="menu_button" id="BSponsors"><a href="https://2010.igem.org/Team:Freiburg_Bioware/Sponsors" target="blank">Sponsors</a></div>
-<div class="menu_button" id="BSafety"><a href="https://2010.igem.org/Team:Freiburg_Bioware/Safty" target="blank">Safety</a></div>
-<div class="menu_button"id="BModelling"><a href="https://2010.igem.org/Team:Freiburg_Bioware/Modelling" target="blank">Modelling</a></div>
 </div>
-</center>
-<!-- Main area -->
-<ul id="index">
-<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/March">March</a></li>
-<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/April">April</a></li>
-<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/May">May</a></li>
-<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/June">June</a></li>
-<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/July">July</a></li>
-<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/August">August</a></li>
-<ul><li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/August2">August Part 2 (labday 99 - 106)</a></li></ul>
-<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/September">September</a></li>
-<ul><li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/September2">September Part 2 (labday 124 - xxx)</a></li></ul>
-<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/October">October</a></li>
-<li><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/November">November</a></li>
-</ul>
 </html>
 ==September==
@@ Line 796: / Line 694: @@
 Trafo was performed according to the standard protocol (XL1blue). The cells were plated on a agar plate with Kana/Cm
 <br>
-====<p style="font-size:15px; background-color:#66bbff;"><b>Sequenzing result of pSB1C3_EGFP_His upper and (!) lower band</b></p>====
+====<p style="font-size:15px; background-color:#66bbff;"><b>Sequencing result of pSB1C3_EGFP_His upper and (!) lower band</b></p>====
 <b>Investigator: Jessica </b><br>
 <b>1. pSB1C3_EGFP_His suffix:</b> <br/>
@@ Line 819: / Line 717: @@
 <br>
 ====<p style="font-size:15px; background-color:#66bbFF;"><b>New aliquots (60µl) of XL1blue can be used !  (Jessica)</b></p>====
-<br/>
+<br />
-<br/>
+===<p style="font-size:17px; background-color:#00dd77;">127. labday 22.09.2010</p>===
+====<p style="font-size:15px; background-color:#66bbff;"><b>Sequencing results of ViralBrick ligations using dephosphorylated vector</b></p>====
+'''Investigator: Achim <br>'''
-<br />
+Sequencing confirmed a correct sequence for clone 11.4 (453 Z34C). Clone 12.1 (587 Z34C)has several missing bases at the 3' end of the insert, clone 13.2 has an a -> c mutation and a c insertion in the insert (although the a->c might be a sequencing error.). Clone 14.2 contained a c deletion.
+We have several new approaches:
+-Correction of the mutations via PCR: We'll use the hybridisation oligo for the side of the insert containing the mutations, the rfc 25 primer on the other side. The amplified insert will be ligated into dephosphorized vector.
+-As a backup, SDM-primers will be ordered and should be available next week.
+-Also, a new colony pcr with several clones from the last ligation plates will be carried out.
+-clone 13.4 (already prepped) will be sent for sequencing
+<br>
-===<p style="font-size:17px; background-color:#00dd77;">127. labday 22.09.2010</p>===
 ====<p style="font-size:15px; background-color:#66bbff;"><b>Cloning pSB1C3_Viral Brick 587KO-empty (B274/P542) into pSB1C3_VP2/3_Capins (B438/P514) </b></p>====
-Investigator Patrick <br>
+'''Investigator Patrick <br>'''
-After an over night digestion with BamHI and PvuII ....
+After an over night digestion with BamHI and PvuII at 37°C ....
 <br>
 [[Image: Mistake.png|thumb|right|100px| My dear friend - what do you mean with "..."?? overnight digest at which temperature?? Did you look it up whether the enzymes show star activity at longer digestions or not?? ;-)]]
@@ Line 847: / Line 755: @@
 Ligation with T4 DNA ligase: 1 µl buffer (10x), 1 µl T4 DNA ligase, 7 µl Vector, 1 µl Insert, 70 minutes.
-The transformation was performed according to the standard protocol and plated: pSB1C3_VP2/3_Capins_587KO-empty
+The transformation with XL1B was performed according to the standard protocol and plated: pSB1C3_VP2/3_Capins_587KO-empty
 ====<p style="font-size:15px; background-color:#66bbff;"><b>Cellculture: Serum-free cells</b></p>====
-Investigator Patrick <br>
+'''Investigator Patrick <br>'''
 We want our virus production to be serum-free to simplify the following purification.  <br>
 ml cell-medium, 25% serum-free: 3,75 ml serum-free DMEM + 11,25 ml DMEM <br>
@@ Line 984: / Line 892: @@
 Transformation was performed according to standard protocol using XL1b cells and Chloramphenicol as antibiotic.
-====<p style="font-size:15px; background-color:#66bbff;"><b>Mini-Prep and test digestion of pSB1C3_001_RC_InsRepCap_KpnIback_VP1-ko</b></p>====
+====<p style="font-size:15px; background-color:#66bbff;"><b>Mini-Prep of pSB1C3_001_RC_InsRepCap_KpnIback_VP1-ko</b></p>====
 <b>Investigator: Stefan</b><br>
@@ Line 1,003: / Line 911: @@
 <li>P549 = pSB1C3_001_RC_InsRepCap_KpnIback_VP1-ko_P5tataless clone 2 c = 409,21 ng/µl</li>
 </ul>
-<b>Test digestion:</b>
-<br />
-<br />
-<b>Results:</b> <br />
-[[Image:new|500px]]
 ====<p style="font-size:15px; background-color:#66bbff;">'''Cloning of CMV promotor into pSB1C3_VP123_inscap'''</p>====
 '''Investigator: Anna'''
-*Vector: name: pSB1C3_VP123_inscap '''P489'''
+*Vector name: pSB1C3_VP123_inscap '''P489'''
-*Insert: name: pSB1C3_CMV '''P193'''
+*Insert name: pSB1C3_CMV '''P193'''
-*new vector name: pSB1C3_CMV_VP123_inscap '''P'''
+*new vector name: pSB1C3_CMV_VP123_capins '''P580'''
 *buffer used: 4
 *DNA concentration (vector): 350,0 ng/µl ; DNA concentration (insert): 333,5 µg/µl
@@ Line 1,020: / Line 922: @@
 <br />
 {| border="1"
-| '''components'''   || align="right" |'''volume of pSB1C3_VP123_inscap /µl''' || align="right" |'''volume of pSB1C3_CMV /µl'''
+| '''components'''   || align="right" |'''volume of pSB1C3_VP123_capins /µl''' || align="right" |'''volume of pSB1C3_CMV /µl'''
 |-
 | DNA  ||  align="right" |3 ||  align="right" |4,5
@@ Line 1,073: / Line 975: @@
 {| border="1"
 |
-!pSB1C3_VP123_inscap_cut
+!pSB1C3_VP123_capins_cut
 !CMV
 |-
@@ Line 1,088: / Line 990: @@
 '''Transformation''': <br>
-XL1B cells were used.
+Was performed following the standard protocol using XL1B cells.
 ====<p style="font-size:15px; background-color:#66bbff;">'''Sequencing of Zegfr:1907-Linker Library, His-Tag and imaging appoaches'''</p>====
@@ Line 1,151: / Line 1,053: @@
 ====<p style="font-size:15px; background-color:#66bbff;"><b>RNA isolation and cDNA synthesis</b></p>====
-Investigator Kira <br>
+'''Investigator Kira <br>'''
 Motivation: in order to figure out if our cell lines do express telomerase, cell pellets were used for RNA isolation.
@@ Line 1,211: / Line 1,113: @@
 ===<p style="font-size:17px; background-color:#00dd77;">128. labday 23.09.2010</p>===
+====<p style="font-size:15px; background-color:#66bbff;"><b>PCR of VB constructs to remove mutations </b></p>====
+'''Investigator Achim<br>'''
+====<p style="font-size:15px; background-color:#66bbff;"><b>Colony PCR of new clones from the last ligations </b></p>====
+'''Investigator Achim<br>'''
+Sequencing of the previously picked clones revealed that the inserts were successfully cloned into pSB1C3. Sadly, apart from 453 Z34C every other insert contained various mutations (deletions, insertions, base exchanges in different positions). The reasons are unclear, probably difficulties with the fill in reaction or incorrectly synthesized oligos. We picked more clones from the last ligations' plates and carried out a colony pcr on them:
+[[Image:Freiburg10 239vblabel2.png|400px|thumb|none|]]
+====<p style="font-size:15px; background-color:#66bbff;"><b>Contuniation: Cloning pSB1C3_Viral Brick 587KO-empty (B274/P542) into pSB1C3_VP2/3_Capins (B438/P514)</b></p>====
+'''Investigator Patrick<br>'''
+Clones were picked in the morning and in each case inoculated 10 ml DYT. Clone 3 didnt grew fast enough. There were not enough bacteria in the eppi even after 8 ml were centrifuged. The mini-prep of clone 1 and 2 was performed according to the standrd protocol yielding the following concentrations:  <br>
+Clone 1: 36,64 ng/µl <br>
+Clone 2: 7,8 ng/µl <br>
+Therefore only clone 1 was sent for sequencing  (labelling: pat1, primer:VR2) and only this clone received a plasmid number: P569 <br>
+No test-digestion was performed. <br>
+Because all medium was used to receive a sufficient amount of bacteria from clone 1 there was no cell suspension left to prepare a glycerol stock. Therefore again each clone was used to inoculated 10 ml DYT, following a mini-prep tomorrow.
+Sequencing results:
+[[Image:Freiburg10_seq_pat1.JPG]]
+Obviously there is something wrong with the backbone or the sequencing.
 ====<p style="font-size:15px; background-color:#66bbff;"><b>Mini-Prep and test digestion of pCerulean_Affibody_VP2/3, pSB1C3_Affibody_middlelinker_EGFP_His, pSB1C3_001_RC_InsRepCap_KpnIback_VP2-ko</b></p>====
@@ Line 1,270: / Line 1,196: @@
 <b>Results:</b> <br />
 [[Image:new123.jpg|500px]]
+* P566 = P565 ; P567 = P566 - P566 is not OK!!!
 * P563 and P566 was sent for sequencing with primer VF2 and VF2/VR2
@@ Line 1,342: / Line 1,269: @@
 Restriction enzymes used: BamHI and PvuI.
+<p style="font-size:13px; color:red;"><b>Comment</b>: </p>
 ====<p style="font-size:15px; background-color:#66bbff;"><b>PCR of Vp1_ex, Vp2_ex and Vp3_ex and cloning into pSB1C3_001</b></p>====
@@ Line 1,392: / Line 1,321: @@
 <p style="font-size:13px; color:red;"><b>Comment</b>:The primer O120 was firstly given to the samples. It's a different primer for the Vp123_suffix, which binds to the regulatory-sequence. Because there was no knowledge, if the Vp_ex constucts have this sequence or not, O92 was also given to the samples.  </p>
 <br>
+<p style="font-size:13px; color:red;"><b>Comment</b>:Because gel-picture showed only DNA within the gel-bags, PCR was repeated.  </p>
+<br>
 <b>Digestion of plasmid backbone:</b> <br />
 Plasmid used: pSB1C3_001 (P320)<br />
@@ Line 1,419: / Line 1,349: @@
 [[Image:Freiburg10 pSb1C3_PAnissa.jpg|500px|]]
-<p style="font-size:13px; color:red;"><b>Comment</b>: </p>
+<p style="font-size:13px; color:red;"><b>Comment</b>:Strangely, PCR-products did not run into the gel, altough the PCR was repeated, after first PCR had two reverse primers in the sample. This could be because of a complex with the polymerase.However, ligation will be continued with the DNA within the bags. </p></br>
 <b>Digestion of PCR product:</b>
 {| border="1"
 | align="left" | '''Components''' ||align="left"| <b>PCR products</b> Volume/µL
 |-
-| align="left" | DNA   ||align="left"| 40
+| align="left" | DNA   ||align="left"| 20
 |-
-| align="left" | BSA (10x) ||align="left"| 6
+| align="left" | BSA (10x) ||align="left"| 3
 |-
-| align="left" | Buffer no. 4 (10x) ||align="left"| 6
+| align="left" | Buffer no. 4 (10x) ||align="left"| 3
 |-
-| align="left" | PstI ||align="left"| 2
+| align="left" | SpeI ||align="left"| 1
 |-
-| align="left" | XbaI ||align="left"| 2
+| align="left" | NgomIV ||align="left"|1
 |-
-| align="left" | H<sub>2</sub>O ||align="left"| 4
+| align="left" | H<sub>2</sub>O ||align="left"| 2
 |-
-| align="left" | '''Total volume''' ||align="left"| <b>60</b>
+| align="left" | '''Total volume''' ||align="left"| <b>30</b>
 |}
 <br />
@@ Line 1,442: / Line 1,372: @@
 <b>PCR-Purification:</b><br />
+*was peformed according the standard-protocol.
 <ul>
-<li>c (P432) = ng/µl</li>
+<li>c (P432) =-- ng/µl</li>
 </ul>
 <br>
-<b>Gel-Extraction:</b><br />
+<p style="font-size:13px; color:red;"><b>Comment</b>:THE WHOLE PCR WILL BE REPEATED ONCE AGAIN  </p>
-Gel-extraction was performed according to standard protocol.<br />
-c(P51.2) = ng/µl
-<b>Ligation:</b> <br />
-<ul>
-<li>1 µl T4 DNA ligase</li>
-<li>1 µl 10x Buffer</li>
-<li>8 µl DNA mix (vector + insert)</li><br>
-</ul>
-Amounts of DNA used:
-<ul>
-<li>(P51.2) =  µl</li>
-<li>(P432) =  µl</li>
-</ul>
-Incubation time: 45 minutes at room temperature. <br />
-<b>Transformation:</b> <br />
-Transformation was performed according to standard protocol using XL1b cells and Chloramphenicol as antibiotic.
 ====<p style="font-size:15px; background-color:#66bbff;"><b>RNA Purity Gel</b></p>====
@@ Line 1,477: / Line 1,388: @@
 ====<p style="font-size:15px; background-color:#66bbff;"><b>hTERT PCR Reaction</b></p>====
-Investigator: Kira <br />
+'''Investigator: Kira <br />'''
+[[Image: Mistake.png|thumb|right|150px| <p style="color:#66bbff;">
+@Kira: Do you think that we can (suggestion?) use the A431 for detection of gene expression driven by phTERT promoter?? We should keep in mind that the transduction efficieny will not be that well ;-) (Bea)</p> ]]
 <br>
@@ Line 1,522: / Line 1,435: @@
 % agarose gel: <br />
+<br>
+Evaluation: The agarose gel reveals that all samples show telomerase activity but in different levels.
 [[Image:Freiburg10_hTERT_PCR.jpg]]
-Evaluation: The agarose gel reveals that all samples show telomerase activity but in different levels.
 ====<p style="font-size:15px; background-color:#66bbff;">'''Cloning of pBAD_Affibody_middlelinker_EGFP_His'''</p>====
 '''Investigator: Jessica'''
@@ Line 1,580: / Line 1,493: @@
 |-
 |}
-<br>
-<br>
+[[Image:Freiburg10 pSb1C3_PAnissa2.jpg|500px|]]
-[[Image:Freiburg10_Cloning_CMV into pBAD_ZEGFR:1907_middlelinker_EGFP_His.jpg|400px]] <br>
-<br/>
 <br/>
 '''Gel extraction''': <br>
@@ Line 1,593: / Line 1,505: @@
 |-
 !DNA-concentration [ng/µl]
+|8,3
+|10,2
+|-
+|}
+<br>
+'''T4 Ligation''': <br>
+Volume vector:  5,06 µl <br>
+Volume insert:  2,94 µl <br>
+<br>
+'''Transformation''': <br>
+XL1B cells were used.
+====<p style="font-size:15px; background-color:#66bbff;">'''Picking clones of pSB1C3_CMV_VP123_inscap'''</p>====
+'''Investigator: Anna'''
+Three clones were picked (10 ml DYT, 10 µl Cm).
+====<p style="font-size:15px; background-color:#66bbff;">'''Cloning of ***** into pSB1C3_CFP'''</p>====
+'''Investigator: Chris W.'''
+*Vector: name: pSB1C3_CFP P51,2
+*Insert: name: email Hybrid Oligo (O184&O185)
+*new vector name: pSB1C3_email
+*buffer used: 4
+*DNA concentration (vector): 151,0 ng/µl ; DNA concentration (insert): 95,3 µg/µl
+[[Image: Mistake.png|thumb|right|150px|Interesting, where does the promoter come from the new annotared vector?? ;-)]]
+<br />
+{| border="1"
+| '''components'''   || align="right" |'''volume of pSB1C3_CFP /µl''' || align="right" |'''volume of email/µl'''
+|-
+| DNA  ||  align="right" |6 ||  align="right" |15
+|-
+| BSA (10x) ||  align="right" |2 ||  align="right" | 2
+|-
+| Buffer 4 (10x)||  align="right" |2||  align="right" |2
+|-
+|Enzyme I||  align="right" |NgoMIV 1 ||  align="right" |NgoMIV 1
+|-
+|Enzyme II||  align="right" |SpeI 1 ||  align="right" |SpeI 1
+|-
+|H2O||  align="right" |8,4 ||  align="right" |-
+|-
+|'''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 120 Volt, running time:45
+<br />
+<br />
+<br />
+'''Loading plan for agarose gel''': <br>
+Loading dye with SDS (6X), 4 µl <br>
+Marker used: GeneRuler ladder mix (Fermentas), 3 µl<br>
+{| border="1"
 |
+!Marker
+!Sample Insert, 20µl
+!Sample Vector, 20µl
+|-
+!Lane
+|1
+|3
+|5
+|-
+!Fragment size
 |
+|70 bp
+|2070 bp
+|-
+|}
+<br>
+<br>
+[[Image:Freiburg10_pSB1C3_001009.jpg|400px]] <br>
+<br/>
+<br/>
+'''Gel extraction''': <br>
+{| border="1"
+|
+!pSB1C3_CFP_cut
+!email
+|-
+!DNA-concentration [ng/µl]
+|7,8
+|27,4
 |-
 |}
 <br>
 '''T4 Ligation''': <br>
-Volume vector:  µl <br>
+Volume vector: 8,74 µl <br>
-Volume insert:  µl <br>
+Volume insert: 0,26 µl <br>
 <br>
 '''Transformation''': <br>
 XL1B cells were used.
-===<p style="font-size:15px; background-color:#66bbff;">'''Picking clones of pSB1C3_CMV_VP123_inscap'''</p>===
+====<p style="font-size:15px; background-color:#66bbff;"><b>Repetition: Cloning of P5_TATAless downstream of pSB1C3_001_RC_insrepcap_KpnI_back and P5 upstream of pSB1C3_001_RC_insrepcap_KpnI_back</b></p>====
+<b>Investigator: Stefan</b>
+<br />
+<b>Digestion of the constructs:</b>
+<ul>
+<li>P432 = pSB1C3_001_RC_insrepcap_KpnI_back c=344,5 ng/µl</li>
+<li>P432 = pSB1C3_001_RC_insrepcap_KpnI_back c=344,5 ng/µl</li>
+<li>P180 = pSB1C3_pTAV2 (P5)clone 1 c=108,8 ng/µl</li>
+<li>P184 = pSB1C3_pAAV_RC (P5TATAless)clone 3 c=176,9 ng/µl</li>
+</ul>
+[[Image:Cartoons48.jpg|200px|thumb|right|My dear friend, did you mix up the Rep-Cap constructs in the plasmid list? P432 = pAAV_RC_insRepCap_KpnI-back ;)]]
+<br />
+{| border="1"
+| align="left" | '''Components''' ||align="left"| <b>V P432up /µL</b> ||align="left"| <b>VP180up /µL</b> ||align="left"| <b>V P432down /µL</b> ||align="left"| <b>V P184down /µL</b>
+|-
+| align="left" | DNA  ||align="left"| 4,5||align="left"|14 ||align="left"| 4,5 ||align="left"|11
+|-
+| align="left" | BSA (10x) ||align="left"| 2||align="left"|2 ||align="left"| 2||align="left"| 2
+|-
+| align="left" | Buffer no. 4 (10x) ||align="left"| 2||align="left"|2 ||align="left"| 2||align="left"| 2
+|-
+| align="left" | Enzyme 1 ||align="left"|XbaI 1||align="left"|SpeI 1 ||align="left"|SpeI 1||align="left"|XbaI 1
+|-
+| align="left" | Enzyme 2 ||align="left"|EcoRI 1||align="left"|EcoRI 1 ||align="left"|PstI 1||align="left"|PstI 1
+|-
+| align="left" | H<sub>2</sub>O ||align="left"| 9,5||align="left"|9,5||align="left"|-||align="left"|3
+|-
+| align="left" | '''Total volume''' ||align="left"| '''20''' ||align="left"| '''20''' ||align="left"| '''20''' ||align="left"| '''20'''
+|-
+|}
+<br />
+<br />
+<b>Results:</b><br />
+[[Image:Freiburg10 cloning P5 P5tataless into pSB1C3 001.jpg|500px]]
+<br />
+<b>Gel-Extraction:</b>
+Gel-Ex was performed according to protocol. The following concentrations were measured:
+<br />
+<ul>
+<li>432up c= 25,73 ng/µl</li>
+<li>180up c= 9,57 ng/µl</li>
+<li>432down c= 27,34 ng/µl</li>
+<li>184down c= 17,80 ng/µl</li>
+</ul>
+<br />
+<b>Ligation:</b><br />
+The following DNA mixes were used for ligation:<br />
+<ul>
+<li>432up V= 6,3 µl</li>
+<li>180up V= 1,7 µl</li><br />
+<br />
+<li>432down V= 6,93 µl</li>
+<li>184down V= 1,07 µl</li>
+</ul>
+<b>Transformation:</b><br />
+The transformation was performed according to standard protocol using BL21 cells. They were plated on agar plates containing chloramphenicol and stored in 37°C room overnight.
+<br />
+<br />
+===<p style="font-size:17px; background-color:#00dd77;">129. labday 24.09.2010</p>===
+====<p style="font-size:15px; background-color:#66bbff;"><b>Sequencing results of VB 13.4</b></p>====
+'''Investigator: Achim<br>'''
+We sent in another clone of the 587 KO Z34C motif to see if it carries the same mutations as the first one. If that had been the case, we could account the mutations to faulty oligos. However, sequencing showed that the second 587 KO Z34C clone is mutated as well, but in different positions. So we either recieved oligos containing various mutations, or the fill-in reaction was faulty in spite of the proofreading activity of the klenow fragment.
+Because 587 KO Z34C is one of our more promising approaches, we sent another two clones from our second colony pcr/clone picking round for sequencing: 13.1 and 13.4
+====<p style="font-size:15px; background-color:#66bbff;"><b>Contuniation: Cloning pSB1C3_Viral Brick 587KO-empty (B274/P542) into pSB1C3_001_VP2/3_Capins (B438/P514)</b></p>====
+'''Investigator Patrick <br>'''
+Because of the sequencing results of clone 1 a mini-prep was performed only with clone 2 and 3 yielding the following concentrations: <br>
+pSB1C3_VP2/3_Capins_587KO-empty clone 2: 195 ng/µl <br>
+pSB1C3_VP2/3_Capins_587KO-empty clone 3: 224,74 ng/µl <br>
+Testdigestion: <br>
+pSB1C3_VP2/3_Capins_587KO-empty clone 2 (P578/B472): 3 µl Buffer 4, 0,5 µl BamHI, 0,5 µl PvuII, 22 µl DNA, 4 µl H2O <br>
+pSB1C3_VP2/3_Capins_587KO-empty clone 3 (P579/B473): 23 µl Buffer 4, 0,5 µl BamHI, 0,5 µl PvuII, 20 µl DNA, 6 µl H2O <br>
+Because somebody switched the 37°C thermoblock off i dont know the exact digestion time. Therefore i switched the thermoblock on again and waited 1 hour. I used that much DNA because the desired insert is 48 bp long.
+[[Image:Freiburg10_0924_pat.jpg]]
+Clone 3 was sent for sequencing.
+====<p style="font-size:15px; background-color:#66bbff;"><b>Sequencing evaluation of VP2/3_Gsat-linker and VP2/3_cap_Gsat-linker</b></p>====
+'''Investigator Kira<br>'''
+[[Image:Freiburg10_Seq_2010_09_24.jpg]]
+'''Comment:''' pSB1C3_VP2/3_cap_Gsat-linker as well as pSB1C3_VP2/3_Gsat-linker can be used for further experiments.
+====<p style="font-size:15px; background-color:#66bbff;"><b>New CD primer ordered</b></p>====
+'''Investigator Stefan<br>'''
+<p style="font-size:13px; color:red;"><b>Comment</b>: CD reverse primer was incorrect. A new primer was ordered. </p>
+<br/>
+====<p style="font-size:15px; background-color:#66bbff;"><b>Sequencing of pCerulean_Zegfr:1907_VP2/3</b></p>====
+'''Investigator Hanna<br>'''
+<br/>
+Because I found out, that this plasmid was sent to GATC with the wrong sequencing primers (therefore no sequencing results were available), I sent it again with the GATC_std_CMV-F primer.<br/>
+--> backbone = pCerulean and not pSB1C3!!! ;)
+====<p style="font-size:15px; background-color:#66bbff;"><b>Repetition: PCR for biobrick production: Cloning RepCap into pSB1C3</b></p>====
+<b>Investigator: Stefan </b>
+<p style="font-size:13px; color:red;"><b>Comment</b>: Construct was cloned mixed RFC10 and RFC25. Therefore, a new approach will be performed consisting of RFC10 only.</p>
+<br>
+Plasmid used:<br />
+<li>pAAV_RC_RepCapIns_SDMKpnI (P432)
+A 1:1000 dilutionof the plasmid was prepared.
+<br />
+<br />
+<b>PCR protocol:</b>
+<br />
+{| border="1"
+| '''Ingredients''' || align="right" | P432 (v/µl)
+|-
+| 5X Phusion HF buffer ||  align="right" |10
+|-
+| 10 mM dNTP mix||  align="right" |1
+|-
+| forward primer: O93 ||  align="right" |2,5
+|-
+| reverse primer: O121 ||  align="right" |2,5
+|-
+| DNA Template||  align="right" |3
+|-
+| DMSO ||  align="right" |-
+|-
+| Phusion Polymerase||  align="right" |0,5
+|-
+|H<sub>2</sub>O||  align="right" |30,5
+|-
+|<b>Total volume</b>||  align="right" |<b>50</b>
+|}
+<br>
+<b>PCR program:</b>
+{| border="1"
+|Cycles||Temperature /°C||Time /s
+|-
+|1||98||60
+|-
+|2 (8x step 2-4)||98||15
+|-
+|3||59||25
+|-
+|4||72||70
+|-
+|5 (17x step 5-6)||98||15
+|-
+|6||72||80
+|-
+|71x||72||300
+|-
+|Hold 4°C
+|}
+<br>
+<b>Digestion of the vector:</b>
+{| border="1"
+| components   || align="right" |pSB1C3_VCK_Bla (P320) (v/µl)
+|-
+| DNA  ||  align="right" |3,5
+|-
+| BSA  ||  align="right" |2
+|-
+| Buffer 4 (10x)||  align="right" |2
+|-
+|SpeI ||  align="right" |1
+|-
+|EcoRI  ||  align="right" |1
+|-
+|H<sub>2</sub>O||  align="right" |10,5
+|-
+|'''Total volume '''||  align="right" |20
+|}
+<br />
+<p style="font-size:13px; color:red;"><b>Comment</b>:Digestion was performed 2 hours at 37 °C.</p><br />
+<br />
+<b>Gel:</b> <br />
+,5 g Agarose,50 ml TAE (1%), 3 µl Gelred , at 110 Volt; run for ~50 minutes<br />
+[[Image:Freiburg10 RC in pSB RFC10.jpg|500px]]<br />
+<br />
+<br />
+<b>Gelextraction:</b><br />
+The gelextraction was performed according to the standard protocol. DNA concentration of the vector:
+<ul>
+<li>pSB1C3 (P320): c= 8,5 ng/µl</li>
+</ul>
+<br/><br/>
+<b>Digestion of the PCR-products:</b>
+{| border="1"
+| components   || align="right" |PCR product (v/µl)
+|-
+| DNA  ||  align="right" |30
+|-
+| BSA  ||  align="right" |4
+|-
+| Buffer 4 (10x)||  align="right" |4
+|-
+|SpeI ||  align="right" |1
+|-
+|EcoRI  ||  align="right" |1
+|-
+|H<sub>2</sub>O||  align="right" |-
+|-
+|'''Total volume '''||  align="right" |40
+|}
+<br />
+<p style="font-size:13px; color:red;"><b>Comment</b>:Digestion was performed 2 hours at 37 °C.</p><br />
+<br />
+<b>PCR purification:</b> <br />
+Purification was performed accoding to the standard protocol. The following concentrations were measured:
+<ul>
+<li>PCR of P432: c= 6,4 ng/µl</li>
+</ul>
+<br>
+<b>Ligation:</b><br />
+µl T4 Ligase buffer (2x)
+µl DNA mix
+µl T4 Ligase
+<br> Incubating for 45 minutes at room temperature.<br />
+<br />
+The  Ligation was performed using the following amounts of DNA:<br />
+<br />
+<ul>
+<li>Vector Volume: 0,92 µl</li>
+<li>Insert Volume: 7,08 µl</li>
+</ul>
+<br>
+<br>
+'''Transformation:'''<br />
+Trafo was performed according to the standard protocol using XL1b cells. The cells were plated on a agar plates containing chlorampenicol.
+<br>
+====<p style="font-size:15px; background-color:#66bbff;">'''Picking clones of pSB1C3_CFP_email'''</p>====
 '''Investigator: Anna'''
+Three clones were picked (10 ml DYT, 10 µl Chloramphenicol).
+====<p style="font-size:15px; background-color:#66bbff;">'''MiniPreps and Test digestion of pSB1C3_CMV_VP123_capins'''</p>====
+'''Investigator: Anna'''
+{| border="1"
+| Sample   || align="right" |Concentration [ng/µl]
+|-
+| pSB1C3_CMV_VP123_capins_clone1  ||  align="right" |377,29
+|-
+|pSB1C3_CMV_VP123_capins_clone2 ||  align="right" |369,92
+|-
+|pSB1C3_CMV_VP123_capins_clone3 ||  align="right" |387,57
+|-
+|}
+<br />
+<b>Test digestion:</b><br />
+{| border="1"
+| Components   || align="right" |Volume /µl
+|-
+| DNA  ||  align="right" |2
+|-
+| BSA  ||  align="right" |-
+|-
+| Buffer 4 (10x)||  align="right" |1
+|-
+|EcoRI ||  align="right" |0,5
+|-
+|NgoMIV  ||  align="right" |0,5
+|-
+|H<sub>2</sub>O||  align="right" |6
+|-
+|'''Total volume '''||  align="right" |10
+|}
+<br />
+<b>Expected size (CFP): 681 bp</b><br />
+[[Image:Freiburg10_Test digestion of pSB1C3_CMV_VP123_capins.jpg|350px]]<br />
+<p style="font-size:13px; color:red;"><b>Comment</b>: Clone 1 was sent for sequencing with the following primers: VF2, 4000 for, 4200 rev, 2800 for and 2800 rev.</p><br />
+====<p style="font-size:15px; background-color:#66bbff;">'''MiniPreps of 587 Z34C ViralBricks and pSB1C3_p40'''</p>====
+'''Investigator: Anna'''
+{| border="1"
+| Sample  || align="right" |Clone || align="right" |Concentration [ng/µl]
+|-
+|pSB1C3_587_KO_Z34C ||  align="right" |13.1||  align="right" |266,97
+|-
+|pSB1C3_587_KO_Z34C ||  align="right" |13.4||  align="right" |277,47
+|-
+|}
+<p style="font-size:13px; color:red;"><b>Comment</b>: Both clones were sent for sequencing.</p><br />
+{| border="1"
+| Sample   || align="right" |Clone|| align="right" |Concentration [ng/µl]
+|-
+|pSB1C3_p40 || align="right" |1||  align="right" |266,97
+|-
+|pSB1C3_p40 || align="right" |2||  align="right" |277,47
+|-
+|pSB1C3_p40 || align="right" |3||  align="right" |167,20
+|-
+|}
+<br />
+====<p style="font-size:15px; background-color:#66bbff;"><b>Re-Trafo of DARPin</b></p>====
+<b>Investigator Stefan</b> <br />
+<p style="font-size:13px; color:red;"><b>Comment</b>: A Re-Trafo of the synthesized DARPin was performed using XL1b cells.</p><br />
+===<p style="font-size:17px; background-color:#00dd77;">130. labday 25.09.2010</p>===
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Sequencing of VB: 13.1, 13.4 (approach w. dephosphorylated vector, second clone picking round</b></p>====
+<b>Investigator: Achim</b>
+The two clones that were sequenced both contained a deletion in the same position in the insert. We really seem to have bad luck picking clones. Hopefully our PCR attempt works better.
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Miniprep of serveral constructs</b></p>====
+<b>Investigator: Jessica</b>
+<b>Glycerol stocks were prepared:</b><br />
+<ul>
+<li>B489 =	pBAD_EGFP_His clone1</li>
+<li>B490 =	pBAD_EGFP_His clone2</li>
+<li>B491 =	pBAD_EGFP_His clone3</li>
+<li>B492 =	pSB1C3_CFP_email clone 1</li>
+<li>B493 =	pSB1C3_CFP_email clone 2</li>
+<li>B494 =	pSB1C3_CFP_email clone 3</li>
+</ul>
+<br />
+<br />
+<b>Mini-Prep was performed according to the standard protocol</b><br />
+<br />
+<ul>
+<li>P588=	pBAD_EGFP_His clone1 c=71,0 ng/µl</li>
+<li>P589 =	pBAD_EGFP_His clone2 c=74,8 ng/µl</li>
+<li>P590 =	pBAD_EGFP_His clone3 c=58,3 ng/µl</li>
+<li>P591 =	pSB1C3_CFP_email clone 1 c=132,7 ng/µl</li>
+<li>P592 =	pSB1C3_CFP_email clone 2 c=168,9 ng/µl</li>
+<li>P593 =	pSB1C3_CFP_email clone 3 c=153,6 ng/µl</li>
+</ul><br />
+<b>Test digestion:</b><br />
+{| border="1"
+| Components   || align="right" |Volume P588-590 /µl|| align="right" |Volume P591-593 /µl|| align="right" |Volume P583-585 /µl
+|-
+| DNA  ||  align="right" |4,5 ||  align="right" |2,5||  align="right" |2
+|-
+| BSA  ||  align="right" |1 ||  align="right" |1 ||  align="right" |1
+|-
+| Buffer 4 (10x)||  align="right" |1||  align="right" |1||  align="right" |1
+|-
+|XbaI ||  align="right" |0,4 ||  align="right" |0,4 ||  align="right" |0,4
+|-
+|PstI  ||  align="right" |0,4||  align="right" |0,4||  align="right" |0,4
+|-
+|H<sub>2</sub>O||  align="right" |2,7 ||  align="right" |4,7||  align="right" |5,2
+|-
+|'''Total volume '''||  align="right" |10||  align="right" |10||  align="right" |10
+|}
+<br />
+<b>Expected size :  bp</b><br />
+[[Image:Freiburg10_Test digestion of minis jessy.jpg|350px]]<br />
+<p style="font-size:13px; color:red;"><b>Comment</b>: test digestion of P591-593 and P583-585 (pSB1C3_P40) is just an attempt because I can't find any sequences in geneious.P583 looks well. P591, P588 and P583 will be sent for sequencing on monday. </p><br />
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Sequencing results of pSb1C3_Affibody_middlelinker_EGFP_His</b></p>====
+[[Image:Freiburg10_sequencing of affi.jpg|350px]]<br />
+<p style="font-size:13px; color:red;"><b>Comment</b>: there was anywhere a problem in the cloning process. approach will be repeated today. there is pBAD_EGFP_His, affibody_middlelinker will be cloned in, also in pSB1C3_EGFP_His</p><br />
+====<p style="font-size:15px; background-color:#66bbff;">'''Sequencing result of pSB1C3_CMV_VP123_capins_clone1'''</p>====
+'''Investigators: Volker, Anna'''
+For test digestion go to labday 24.09.10
+[[Image:Freiburg10_Sequencing of pSB1C3_CMV_VP123_capins.jpg|500px]]<br />
+<p style="font-size:13px; color:red;"><b>Comment</b>: The following primers were used for sequencing: VF2, 4000 for, 4200 rev, 2800 for and 2800 rev. There is a point mutation in the non-coding sequence, which should not influence the performence of the construct, so it can be used for further cloning steps.</p><br />
+====<p style="font-size:15px; background-color:#66bbff;">'''Cloning of 453 and 587 ViralBricks into pSB1C3_CMV_VP123_capins'''</p>====
+'''Investigators: Achim, Anna'''
+*Vector name: pSB1C3_CMV_VP123_capins '''P580'''
+*Inserts: different ViralBricks (see pdf underneath), pSB1C3_VCK_Bla '''P320'''
+*buffer used: 4
+<p style="font-size:13px; color:red;"><b>Update</b>: ViralBricks ready to use:</p>
+[[media:Freiburg10_Production of ViralBricks_new.pdf]]<br />
+<br />
+<b>Digestion of vector and inserts:</b><br />
+[[media:Freiburg10_Cloning of ViralBricks into pSB1C3_CMV_VP123_capins.pdf]]<br />
+The vector p580 was dephosphorylated.<br />
+Two gels were prepared with 1 g Agarose, 100 ml TAE (1%) and 6 µl GELRED; at 120 Volt, running time:45
+<br />
+'''Gel run''': <br>
+Loading dye(6X), 6 µl <br>
+Marker used: GeneRuler ladder mix (Fermentas), 3 µl<br>
+Expected sizes of fragments: see Pdf under '''Gel extraction and overnight T4 Ligation'''
+<br>
+<br>
+[[Image:Freiburg10_Digestion of ViralBricks_Cloning into pSB1C3_CMV_VP123_capins.jpg|400px]]<br/>
+[[Image:Freiburg10_Digestion of ViralBricks and pSB1C3_CMV_VP123_capins.jpg|400px]] <br>
+<br/>
+<br/>
+'''Gel extraction and overnight T4 Ligation''': <br>
+[[media:Freiburg10_Cloning of ViralBricks into pSB1C3_CMV_VP123_capinsII.pdf]]<br />
+====<p style="font-size:15px; background-color:#66bbff;">'''Sequencing results: pSB1C3_001_VP2/3_HSPG-KO'''</p>====
+'''Investigator: Hanna''' <br/>
+<br/>
+<b>Comment:</b> In order to knock down the natural tropism of the virus, the HSPG knock-out motif (two aa exchanges) was cloned into VP2/3. This fragment can then be used for the VP2 N-terminal fusion or VP1 insertion approaches. <br/>
+<br/>
+[[Image:Freiburg10 pSB1C3 VP23-HSPG-KO.png|500px]]
+<br/>
+Conclusion: Sequencing results looked well: The HSPG-KO ViralBrick was cloned successfully into VP2/3. <br/>
+====<p style="font-size:15px; background-color:#66bbff;">'''Cloning of pBAD_Affibody_middlelinker_EGFP_His and pSB1C3_Affibody_middlelinker_EGFP_His'''</p>====
+'''Investigator: Jessica''' <br>
+<b>Comment: There was a mistake in cloning pSB1C3_Affibody_middlelinker_EGFP_His so there is just pSB1C3_EGFP_His. in this plasmid will be cloned Affibody_middlelinker, also in pBAD_EGFP_His</b> <br/>
+*Vector: name: pBAD_EGFP_His  '''P588'''
+*Vector: name: pSB1C3_EGFP_His  '''P565'''
+*Insert: name: pSB1C3_ZEGFR:1907_middlelinker_ '''P290'''
+*new vector name: pBAD_ZEGFR:1907_middlelinker_EGFP_His '''P'''
+*new vector name: pSb1C3_ZEGFR:1907_middlelinker_EGFP_His '''P'''
+*buffer used: 4
+*DNA concentration (vector): 71,0 ng/µl / 252,7 ng/µl; DNA concentration (insert): 227,4 µg/µl
+<br />
+{| border="1"
+| '''components'''   || align="right" |'''volume of pBAD_EGFP_His  /µl''' || align="right" |'''volume of pSB1C3_EGFP_His /µl'''  || align="right" |'''volume of pSB1C3_ZEGFR:1907_middlelinker /µl'''
+|-
+| DNA  ||  align="right" |15 ||  align="right" |4  ||  align="right" |7
+|-
+| BSA (10x) ||  align="right" |2 ||  align="right" | 2 ||  align="right" | 2
+|-
+| Buffer 4 (10x)||  align="right" |2||  align="right" |2  ||  align="right" | 2
+|-
+|Enzyme XbaI||  align="right" |0,8 ||  align="right" |0,8 ||  align="right" |0,8
+|-
+|Enzyme AgeI||  align="right" |- ||  align="right" |- ||  align="right" |0,8
+|-
+|Enzyme NgoMIV||  align="right" |0,8 ||  align="right" |0,8 ||  align="right" |-
+|-
+|H2O||  align="right" |-||  align="right" |10,4||  align="right" |7,4
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 20,6||  align="right" |20 ||  align="right" |20
+|}
+<br />
+,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 120 Volt
+<br />
+<br />
+{| border="1"
+|
+!Marker
+!P290, 20µl
+!P565, 20µl
+!P588, 20µl
+|-
+!Sample
+|4
+|1
+|2
+|3
+|-
+!Fragment size
+|
+|210 bp
+|2800 bp
+|4700 bp
+|-
+|}
+<br/>
+[[Image:Freiburg10_Cloning of PSB1C3_pBad_Affibody_middlelinker_EGFP_His.jpg|150px|]]
+<br/>
+'''Gel extraction''': <br>
+{| border="1"
+|
+!pBAD
+!pSB1C3
+!Affibody_middlelinker
+|-
+!DNA-concentration [ng/µl]
+|
+|
+|
+|-
+|}
+<br>
+'''T4 Ligation pBAD''': <br>
+Volume vector:  3,5 µl <br>
+Volume insert:  4,5 µl <br>
+<br>
+<br>
+'''T4 Ligation pSB1C3''': <br>
+Volume vector:  2,3 µl <br>
+Volume insert:  5,7 µl <br>
+<br>
+===<p style="font-size:17px; background-color:#00dd77;">131. labday 26.09.2010</p>===
+====<p style="font-size:15px; background-color:#66bbff;">'''Continuation of cloning of pBAD_Affibody_middlelinker_EGFP_His and pSB1C3_Affibody_middlelinker_EGFP_His'''</p>====
+'''Transformation''': <br>
+BL21 cells were used - in 37°C at 8.30am
+* pBAD_Affibody_middlelinker_EGFP_His
+* pSB1C3_Affibody_middlelinker_EGFP_His<br>
+<p style="font-size:13px; color:red;"><b>Comment</b>:pSB1C3_Affibody_middlelinker_EGFP_His was not successful (no colonies on plate), will be repeated on monday</p>
+====<p style="font-size:15px; background-color:#66bbff;">'''Picking clones of different constructs'''</p>====
+<b>Investigator: Anna </b><br/>
+Clones were picked of:<br/>
+*pBad_Affibody_middlelinker_EGFP_His<br/>
+*pSB1C3_001_RC_InsRepCap_KpnIback_RFC10<br/>
+*Darpin (ReTrafo)<br/>
+*pSB1C3_453_BAP (p402, ReTrafo)
+*pSB1C3_587_KO_RGD (p390, ReTrafo)
+*pSB1C3_587_KO_His (p391, ReTrafo)
+In addition, preparations for Mini-Preps of several ViralBricks were done:
+*B289: 587_BAP
+*B270: 587_KO_BAP
+*B271: 587_RGD
+*B272: 453_His
+*B273: 587_His
+*B274: 587_KO_empty
+*B488: 453_Z34C
+<p style="font-size:13px; color:red;"><b>Comment</b>: Inoculating of 10 mL DYT medium containing 10µL chloramphenicol (except pBad with Amp).<br/>
+There were no clones on the plate with pSB1C3_Affibody_middlelinker_EGFP_His. </p>
+====<p style="font-size:15px; background-color:#66bbff;">'''Continuation of cloning of 453 and 587 inserts into pSB1C3_CMV_VP123_capins'''</p>====
+<b>Investigator: Achim, Anna</b>
+<br>
+<b>Transformation</b>: <br>
+Trafo was performed according to the standard protocol using XL1b cells. The cells were plated on agar plates containing chlorampenicol and stored in the 37°C room.
+<br>
+====<p style="font-size:15px; background-color:#66bbff;">'''Colony PCR of remaining 587 constructs'''</p>====
+<b>Investigator: Achim, Anna</b>
+<p style="font-size:13px; color:red;"><b>Comment</b>: New clones of the remaining 587 constructs were picked (from new cloning approach with T4 Ligation and dephosphorylated vector, see labdays 15.09. and 22.09.). </p>
+<br />
+Constructs:
+*12: 587_Z34C
+*13: 587_KO_Z34C
+*14: 587_Z34C_KO_Spacer
+<br />
+{| border="1"
+| '''Components'''   || align="right" |'''Volume /µl'''
+|-
+| 10x Standard Taq Buffer (with MgCl2)  ||  align="right" |1
+|-
+| MgCl2 (50mM) ||  align="right" |0,1
+|-
+| dNTPs||  align="right" |0,2
+|-
+|Primer 1: RFC25 for ||  align="right" |0,2
+|-
+|Primer 2: RFC25 rev||  align="right" |0,2
+|-
+|Taq Polymerase||  align="right" |0,05
+|-
+|H2O||  align="right" |8,25
+|-
+|'''Total volume'''||  align="right" | 10
+|}
+<br />
+{| border="1"
+| '''Cycles'''   || align="right" |'''Temperature'''  || align="right" |'''Time'''
+|-
+|   ||  align="right" |95°C ||  align="right" |6 min
+|-
+| 30x ||  align="right" |95°C ||  align="right" |25 sec
+|-
+|(Tm -3°C)||  align="right" |60°C||  align="right" |30 sec
+|-
+|1 min/kb||  align="right" |68°C ||  align="right" |55 sec
+|-
+|1x||  align="right" |68°C||  align="right" |5 min
+|-
+|Hold 4°C||  align="right" | ||  align="right" |
+|-
+|}
+[[Image:Freiburg10_Colony PCR of constructs 12-14.jpg|350px|]]
+<br />
+<p style="font-size:13px; color:red;"> Clone 13.3, 14.1 and 14.3 will be sent for sequencing.<br/></p>
+====<p style="font-size:15px; background-color:#66bbff;">'''Sequencing results: pCerulean_Zegfr:1907_VP2/3'''</p>====
+<b>Investigator: Hanna </b>
+<br/>
+[[Image:Freiburg10 pCerulean Affi VP23.png|700px|thumb|center]] <br/>
+<br/>
+Sequencing results revealed that VP2/3 (unmodified!) was successfully fused to the Affibody (without linker). <br/>
+Next step: Fusion of VP2/3-HSPG-KO to the C-terminus of the Affibody.
+<br/>
+<br/>
+====<p style="font-size:15px; background-color:#66bbff;">'''N-terminal VP2-Fusion & VP1 Insertion: Fusion of VP2/3_HSPG-KO'''</p>====
+<b>Investigator: Hanna </b>
+<br/>
+<p scolor:#80080;"><b>Comment:</b> In order to target tumor cells with our AAV2 two VP2 fusion strategies were figuered out: The so called VP2-fusion and VP1 insertions. These approaches were successfully cloned and are now tested in cell culture. In order to prevent targeting of other (healthy) cells, the natural tropism of the virus needs to be knocked down. For this purpose a ViralBrick, "587-KO_empty", was designed and cloned into pSB1C3_001_VP2/3_Capins. <br/>
+Today this VP2/3_HSPG-KO sequence will be fused to the N-terminus of the Affibody, CFP/mVenus and His-Tag of both, the N-terminal fusion to VP2 and the VP1 insertion, approach. </p>
+<br/>
+<br/>
+<b>DIGESTION:</b> <br/>
+<br/>
+. pCerulean_CFP_MiddleLinker (P407)<br/>
+. pCerulean_Z<sub>EGFR:1907</sub>_MiddleLinker (P408)<br/>
+. pCerulean_Z<sub>EGFR:1907</sub>_SEG (P409)<br/>
+. pCerulean_Z<sub>EGFR:1907</sub>_ShortLinker (P410)<br/>
+. pCerulean_Z<sub>EGFR:1907</sub>_LongLinker (P412)<br/>
+. pCerulean_6xHis_MiddleLinker (P374)<br/>
+. pCerulean_VP1up_NLS_Z<sub>EGFR:1907</sub> (P422)<br/>
+. pCerulean_VP1up_NLS_6xHis (P424)<br/>
+. pCerulean_VP1up_NLS_mVenus (P426)<br/>
+.1 pSB1C3_001_Vp2/3_HSPG-KO (P579)<br/>
+.2 pSB1C3_001_Vp2/3_HSPG-KO (P579)<br/>
+<br/>
+[[Image:Freiburg10 Digestion 26 9.jpg|500px|thumb|center]] <br/>
+<br/>
+Incubation: 2 hours, 37°C. <br/>
+Agarose gel: 0.8% <br/>
+<br/>
+{| border="1" cellspacing="0" cellpadding="2" bordercolor="black"
+!Sample
+!Sample/µl]
+!Loading dye (6x)/µl
+!Expected size
+|--
+|1
+|20 µl
+|4 µl
+|4710 bp
+|--
+|2
+|20 µl
+|4 µl
+|4169 bp
+|--
+|3
+|20 µl
+|4 µl
+|4254 bp
+|--
+|4
+|20 µl
+|4 µl
+|4158 bp
+|--
+|5
+|20 µl
+|4 µl
+|4181 bp
+|--
+|6
+|20 µl
+|4 µl
+|2129 bp
+|--
+|7
+|20 µl
+|4 µl
+|4583 bp
+|--
+|8
+|20 µl
+|4 µl
+|4428 bp
+|--
+|9
+|20 µl
+|4 µl
+|5124 bp
+|--
+|10.1
+|20 µl
+|4 µl
+|1937 bp
+|--
+|10.2
+|20 µl
+|4 µl
+|1937 bp
+|--
+|}
+{| align=right
+|}
+<br />
+*Marker: GeneRuler ladder mix
+{| border="1"
+|
+!Marker /µL
+!Sample 1 /µl
+!Sample 2 /µl
+!Sample 3 /µl
+!Sample 4 /µl
+!Sample 5 /µl
+!Sample 6 /µl
+!Sample 7 /µl
+!Sample 8 /µl
+!Sample 9 /µl
+!Sample 10.1 /µl
+!Sample 10.2 /µl
+|-
+!Lane
+|4.5
+|24
+|24
+|24
+|24
+|24
+|24
+|24
+|24
+|24
+|36
+|36
+|-
+|}
+<br />
+<br/>
+[[Image:Freiburg10 Gel1 26-9-10.png|500px|thumb|center]]<br/>
+[[Image:Freiburg10 Gel2 26-9-10.png|500px|thumb|center]] <br/>
+<br/>
+<b>LIGATION:</b>
+<br />
+[[Image:Freiburg10 26 9 10 Konz.png|500px|thumb|center]]<br/>
+[[Image:Freiburg10 26 9 10 Liagtion.png|500px|thumb|center]]
+<br />
+<br/>
+<b>TRAFO:</b>  <br/>
+Trafo was performed following our standard protocol. Cells: XL1b, DNA: 2µL. <br/>
+Plates will be stored over night @ the 37°C room. <br/>
+<br/>
+<b>Next step:</b> Picking 2 clones of each construct, colony PCR!
+<br/>
+===<p style="font-size:17px; background-color:#00dd77;">132. labday 27.09.2010</p>===
+====<p style="font-size:15px; background-color:#66bbff;">'''Sent for sequencing'''</p>====
+<b>Investigator: Jessica </b><br>
+*P591 pSB1C3_email: VR2
+*P583 pSB1C3_P40: VR2
+*P588 pBAD_EGFP_His: pBAD-FP
+*P596 pBAD_Affibody_middlelinker_EGFP_His: pBAD-FP / pTrcHis-RP
+<br/>
+====<p style="font-size:15px; background-color:#66bbff;"><b>Picking clones of VP1 insertion and VP2 fusion HSPG-KO approaches</b></p>====
+<b>Investigator: Hanna</b>
+<br/>
+clones were picked of each ligation approach = 18 falcons (Kanamycin).<br/>
+<br/>
+To do: Mini-Prep and test digestion - sequencing.
+<br />
+====<p style="font-size:15px; background-color:#66bbff;">'''MiniPreps of different constructs'''</p>====
+<b>Investigator: Anna </b><br/>
+The following constructs were prepped according to the standard protocol:
+*pSB1C3_453_BAP (p402, ReTrafo)
+*pSB1C3_587_KO_RGD (p390, ReTrafo)
+*pSB1C3_587_KO_His (p391, ReTrafo)
+*B289: 587_BAP
+*B290: 453_RGD
+*B270: 587_KO_BAP
+*B271: 587_RGD
+*B272: 453_His
+*B273: 587_His
+*B274: 587_KO_empty
+*B488: 453_Z34C
+*B473:
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Miniprep of serveral constructs</b></p>====
+<b>Investigator: Stefan</b>
+<b>Glycerol stocks were prepared:</b><br />
+<ul>
+<li>B489 =	pSB1C3_001_RC_InsRepCap_KpnIback_RFC10  clone 1</li>
+<li>B490 =	pSB1C3_001_RC_InsRepCap_KpnIback_RFC10  clone 2</li>
+<li>B491 =	pBAD_Affibody_middlelinker_EGFP_His clone 1</li>
+<li>B492 =	pBAD_Affibody_middlelinker_EGFP_His clone 2</li>
+<li>B493 =	pBAD_Affibody_middlelinker_EGFP_His clone 3</li>
+</ul>
+<br />
+<br />
+<b>Mini-Prep was performed according to the standard protocol</b><br />
+<br />
+<ul>
+<li>P594=	pSB1C3_001_RC_InsRepCap_KpnIback_RFC10  clone 1 c= 140,9 ng/µl</li>
+<li>P595 =	pSB1C3_001_RC_InsRepCap_KpnIback_RFC10  clone 2 c= 117,5 ng/µl</li>
+<li>P596 =	pBAD_Affibody_middlelinker_EGFP_His clone 1 c= 101,4 ng/µl</li>
+<li>P597 =	pBAD_Affibody_middlelinker_EGFP_His clone 2 c= 92,9 ng/µl</li>
+<li>P598 =	pBAD_Affibody_middlelinker_EGFP_His clone 3 c= 92,1 ng/µl</li>
+</ul><br />
+<b>Test digestion:</b><br />
+{| border="1"
+| Components   || align="right" |Volume P594+P595 /µl|| align="right" |Volume P596-598 /µl
+|-
+| DNA  ||  align="right" |2,5 ||  align="right" |2,5|
+|-
+| BSA  ||  align="right" |1 ||  align="right" |1
+|-
+| Buffer 4 (10x)||  align="right" |1||  align="right" |1
+|-
+|XbaI ||  align="right" |0,4 ||  align="right" |0,4
+|-
+|PstI  ||  align="right" |0,4||  align="right" |0,4
+|-
+|H<sub>2</sub>O||  align="right" |4,7 ||  align="right" |4,7
+|-
+|'''Total volume '''||  align="right" |10||  align="right" |10
+|}
+<br />
+[[Image:Freiburg10 test digestion InsRepCap KpnIback RFC10 pBAD Affi Middle EGFP His.jpg|450px]]<br />
+<p style="font-size:13px; color:red;"><b>Comment</b>:</p><br />
+====<p style="font-size:15px; background-color:#66bbff;"><b>Re-Trafo of pSB1C3_pTAV (P5)</b></p>====
+<b>Investigator: Stefan </b><br>
+<p style="font-size:13px; color:red;"><b>Comment</b>:After inocculating from glycerol-stock, the plasmid showed strange results during digestion. Therefore a re-trafo will have to be performed to replace the stock.</p><br />
+====<p style="font-size:15px; background-color:#66bbff;"><b>Repetition: Cloning of P5_TATAless downstream of pSB1C3_001_RC_insrepcap_KpnI_back and P5 upstream of pSB1C3_001_RC_insrepcap_KpnI_back</b></p>====
+<b>Investigator: Stefan</b>
+<br />
+<b>Digestion of the constructs:</b>
+<ul>
+<li>P594 = pSB1C3_001_RC_insrepcap_KpnI_back c=344,5 ng/µl</li>
+<li>P594 = pSB1C3_001_RC_insrepcap_KpnI_back c=344,5 ng/µl</li>
+<li>P586 = pSB1C3_pTAV2 (P5)clone 1 c=137,37 ng/µl</li>
+<li>P587 = pSB1C3_pAAV_RC (P5TATAless)clone 3 c=191,61 ng/µl</li>
+</ul>
+<br />
+{| border="1"
+| align="left" | '''Components''' ||align="left"| <b>V P594up /µL</b> ||align="left"| <b>VP586up /µL</b> ||align="left"| <b>V P594down /µL</b> ||align="left"| <b>V P587down /µL</b>
+|-
+| align="left" | DNA  ||align="left"| 10||align="left"|14 ||align="left"| 10 ||align="left"|13
+|-
+| align="left" | BSA (10x) ||align="left"| 2||align="left"|2 ||align="left"| 2||align="left"| 2
+|-
+| align="left" | Buffer no. 4 (10x) ||align="left"| 2||align="left"|2 ||align="left"| 2||align="left"| 2
+|-
+| align="left" | Enzyme 1 ||align="left"|XbaI 1||align="left"|SpeI 1 ||align="left"|SpeI 1||align="left"|XbaI 1
+|-
+| align="left" | Enzyme 2 ||align="left"|EcoRI 1||align="left"|EcoRI 1 ||align="left"|PstI 1||align="left"|PstI 1
+|-
+| align="left" | H<sub>2</sub>O ||align="left"| 9,5||align="left"|9,5||align="left"|-||align="left"|3
+|-
+| align="left" | '''Total volume''' ||align="left"| '''20''' ||align="left"| '''20''' ||align="left"| '''20''' ||align="left"| '''20'''
+|-
+|}
+<br />
+<br />
+<b>Results:</b><br />
+[[Image:Freiburg10 digestion cloning P5tataless downstream RepSDMCap.jpg|500px]]
+<p style="font-size:13px; color:red;"><b>Comment</b>:P5 and P5TATAless do not fit the expected results. For P5TATAless, a new digestion using the P184 plasmid was performed. For P5 no old plasmid stock was available, therefore a re-trafo will have to be performed.</p><br />
+{| border="1"
+| align="left" | '''Components''' ||align="left"| <b>V P184down /µL</b>
+|-
+| align="left" | DNA  ||align="left"| 10
+|-
+| align="left" | BSA (10x) ||align="left"| 2
+|-
+| align="left" | Buffer no. 4 (10x) ||align="left"| 2
+|-
+| align="left" | XbaI ||align="left"| 1
+|-
+| align="left" | PstI ||align="left"| 1
+|-
+| align="left" | H<sub>2</sub>O ||align="left"| 4
+|-
+| align="left" | '''Total volume''' ||align="left"| <b>20</b>
+|-
+|}
+<p style="font-size:13px; color:red;"><b>Comment</b>:No gel picture available because computer crashed completely...</p><br />
+<br />
+<b>Gel-Extraction:</b><br />
+Gel-Ex was performed according to protocol. The following concentrations were measured:
+<br />
+<ul>
+<li>594down c= 29,9 ng/µl</li>
+<li>184down c= 3,8 ng/µl</li>
+</ul>
+<br />
+<b>Ligation:</b><br />
+The following DNA mixes were used for ligation:<br />
+<ul>
+<li>432down V= 4,48 µl</li>
+<li>184down V= 3,52 µl</li>
+</ul>
+<br />
+<b>Transformation:</b><br />
+The transformation was performed according to standard protocol using BL21 cells. They were plated on agar plates containing chloramphenicol and stored in 37°C room overnight.
+<br />
+<br />
+====<p style="font-size:15px; background-color:#66bbff;"><b>Picking clones of VP1 insertion and VP2 fusion HSPG-KO approaches</b></p>====
+<b>Investigator: Hanna</b>
+<br/>
+clones were picked of each ligation approach = 18 falcons (Kanamycin).<br/>
+<br/>
+To do: Mini-Prep and test digestion - sequencing.
+<br />
+====<p style="font-size:15px; background-color:#66bbff;"><b>Picking clones of VP1 insertion and VP2 fusion HSPG-KO approaches</b></p>====
+<b>Investigator: Hanna</b>
+<br/>
+clones were picked of each ligation approach = 18 falcons (Kanamycin).<br/>
+<br/>
+To do: Mini-Prep and test digestion - sequencing.
+<br />
+===<p style="font-size:17px; background-color:#00dd77;">133. labday 28.09.2010</p>===
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Cloning of the ViralBricks BAP-HSPG-ko and His-HSPG-ko into pSB1C3_VP2/3</b></p>====
+<b>Investigator: Bea</b>
+<br/>
+<p style="color:#66bbff;"><i>Comment</i>: After discussing the finals constructs, we decided to clone HSPG-KO with BAP and His motifs into the N-terminal approaches which means that the plasmids pCerulean_Targeting_VP2/3 contains His and BAP ViralBricks integrated in the 587 loop, respectively. Therefore I started the first cloning step in order to obtain the fully assembled targeting construct which can be cotransfected with the plasmids containing rep and cap genes (with or wihtout HSPG-ko) </p>
+<br />
+<b>Digestion of the constructs:</b>
+<ul>
+<li>P604 = pSB1C3_001_587-ko_BAP </li>
+<li>P606 = pSB1C3_001_587-ko_His</li>
+<li>P525 = pSB1C3_001_VP2/3capins</li>
+</ul>
+<br />
+{| border="1"
+| align="left" | '''Components''' ||align="left"| <b>v<sub>P606</sub> /µL</b> ||align="left"| <b>v<sub>P525 upstream</sub>/µL</b> ||align="left"| <b>v<sub>P604</sub> /µL</b>
+|-
+| align="left" | DNA  ||align="left"| 21||align="left"|6 ||align="left"|18
+|-
+| align="left" | BSA (10x) ||align="left"| 4||align="left"|2 ||align="left"| 4
+|-
+| align="left" | Buffer no. 4 (10x) ||align="left"| 4||align="left"|2 ||align="left"| 4
+|-
+| align="left" | Enzyme 1 ||align="left"|BamHI||align="left"|BamHI ||align="left"|BamHI
+|-
+| align="left" | Enzyme 2 ||align="left"|SpeI||align="left"|PvuII||align="left"|PvuII
+|-
+| align="left" | H<sub>2</sub>O ||align="left"|9||align="left"|8||align="left"|12
+|-
+| align="left" | '''Total volume''' ||align="left"| '''40''' ||align="left"| '''20''' ||align="left"| '''40'''
+|-
+|}
+<br />
+<br />
+<b>Loading plan of a 1% agarose gel:</b>
+<br/>
+ M    P525
+<b>Loading plan of a 2% agarose gel:</b>
+ M    P604    P606
+<br/>
+<b>Expected sizes of the digested products are:</b>
+<ul>
+<li> P525= 48<b>,3800 bp</b></li>
+<li> P604= 2216, <b>81bp</b></li>
+<li> P606 = 2216, <b>108bp</b></li>
+</ul>
+<br />
+<b>Results:</b>
+[[Image: Freiburg10_VP23-BAP_KO_and_His_KO_28.09.2010.png|thumb|center|400px]]
+<br />
+After gel extraction has been performed, the 2µL of each ligated plasmids were transformed into BL-21 cells.
+====<p style="font-size:15px; background-color:#66bbff;"><b>Test digestion: ViralBricks in pSB1C3_CMV_VP123_capins</b></p>====
+<b>Investigator: Achim </b><br>
+*We digested preps of all our 453 Inserts with BamHI & SspI and all our 587 Inserts with SalI and PvuII. That way we get bands of ~50 bp difference between our loop inserts and the wt loop region. (Eg. 453 BAP: 455 with insert, 396 without insert.)
+*Nomenclature as in previous VB assays.
+*Clone 11.2 is missing , I forgot to inoculate it.
+*P580 (pSB1C3_CMV_VP123_capins)
+[[Image:Freiburg10 29.9 1.png|thumb|none|500px|The framed samples were midiprepped and will be used for transfection]]
+====<p style="font-size:15px; background-color:#66bbff;"><b>Sequencing result of pSB1C3_email and pBAD_Affibody_middlelinker_EGFP_His</b></p>====
+<b>Investigator: Jessica </b><br>
+<b>1. pSB1C3_email:</b> <br/>
+[[Image:Freiburg10 GFPHis1.jpg|600px|thumb|center|]] <br/>
+<b>2. pBAD_Affibody_middlelinker_EGFP_His:</b> <br/>
+[[Image:Freiburg10 GFPHis3.jpg|600px|thumb|center|]] <br/>
+====<p style="font-size:15px; background-color:#66bbff;"><b>Preparation of PBS Buffer and PBS Buffer with Imidazole</b></p>====
+'''Investigator: Jessica'''
+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>4</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
+<br>
+*dissolve the following in 180ml ddH<sub>2</sub>O:
+**6,4g of NaCl
+**0,16g of KCl
+**1,15g of Na<sub>2</sub>HP0<sub>4</sub> (1.69 because of the crystal water in the reagent)
+**0,19 g of KH<sub>2</sub>PO<sub>4</sub>
+**3,4g of Imidazole
+*adjust to pH 7.4
+*adjust to 200ml
+*steril filtrate the solution
+====<p style="font-size:15px; background-color:#66bbff;"><b>ViralBrick Sequencing results: pSB1C3_587_KO_Z34C and pSB1C3_587_KO_Z34C_Spacer</b></p>====
+'''Investigator: Achim'''
+Sequencing showed that the PCR reaction we designed to remove the mutations in the z34c insert were successful! Both  pSB1C3_587_KO_Z34C and pSB1C3_587_KO_Z34C_Spacer are correct. We hadn't sent the 587_Z34C for sequencing because the colony PCR hadn't shown any bands. But because this construct is less important for cell culuture, we won't continue working on this construct. <br />
+====<p style="font-size:15px; background-color:#66bbff;"><b>Cloning of Darpin into pCerulean_Vp1up_NLS and pSB1C3 </b></p>====
+'''Investigator: Achim'''
+*The Darpin needs to be cloned into pSB1C3 for submission to the parts registry as well as into pCerulean for expression.
+*Darpin ( cut with NgOMIV & SpeI
+*Vectors cut with AgeI & SpeI
+**-> Results in fusion protein
+[[Image:Freiburg10 280910AS.JPG|none|thumb|150px]]
+====<p style="font-size:15px; background-color:#66bbff;">'''Cloning of pSB1C3_001_CMV and pSB1C3_001_Vp2/3_HSPG-Ko_CMV_ZEGFR:1907'''</p>====
+'''Investigator: Anissa''' <br>
+<b>Comment: By working with three-fragment-ligation, CMV and ZEGFR:1907 will each be cut out of pSB1C3, will be ligated together and into the vector pSB1C3_001_Vp2/3_HSPG-Ko. Additionally, CMV will be cloned freom pSB1C3 into pSB1C3_001  </b> <br/>
+*Vector: name:pSB1C3_001_Vp2/3_HSPG-Ko '''P613''' c=273,6 ng/µl
+*Vector: name: pSB1C3_001_bla  '''P320''' c=408 ng/µl
+*Insert: name: pSB1C3_CMV '''P146''' c=155,6 ng/µl
+*Insert: name: pSB1C3_ZEGFR:1907 '''P268''' c=162,5 ng/µl
+*new vector name: pSB1C3_001_CMV
+*new vector name: pSB1C3_001_Vp2/3_HSPG-Ko_CMV_ZEGFR:1907
+*buffer used: 4
+<br />
+{| border="1"
+| '''components'''   || align="right" |'''pSB1C3_CMV /µl'''|| align="right" |'''pSB1C3_ZEGFR:1907  /µl''' || align="right" |'''volume of pSB1C3_001_bla /µl'''  || align="right" |'''volume of pSB1C3_001_Vp2/3_HSPG-Ko/µl'''
+|-
+| DNA  ||  align="right" |12,7 ||  align="right" |12,3  ||  align="right" | 3,6||  align="right" |5,5
+|-
+| BSA (10x) ||  align="right" |2 ||  align="right" | 2 ||  align="right" |1,5 ||  align="right" |1,5
+|-
+| Buffer 4 (10x)||  align="right" |2||  align="right" |2  ||  align="right" |1,5 ||  align="right" |1,5
+|-
+|Enzyme SpeI||  align="right" |1||  align="right" |- ||  align="right" |1||  align="right" |-
+|-
+|Enzyme EcoRI||  align="right" |1 ||  align="right" |- ||  align="right" |1||  align="right" |1
+|-
+|Enzyme XbaI||  align="right" |- ||  align="right" |1 ||  align="right" |-||  align="right" |-
+|-
+|Enzyme AgeI||  align="right" |- ||  align="right" |1 ||  align="right" |-||  align="right" |-
+|-
+|Enzyme NgoMIV||  align="right" |-||  align="right" |-||  align="right" |-||  align="right" |1
+|-
+|H2O||  align="right" |1,3||  align="right" |1,7||  align="right" |6,4||  align="right" |4,5
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 20||  align="right" |20 ||  align="right" |15||  align="right" |15
+|}
+<br />
+,5 g Agarose, 55 ml TAE (1%), 1,5 µl GELRED , at 115Volt
+<br />
+<br />
+{| border="1"
+|
+!Marker
+!P146, 20µl
+!P268, 20µl
+!P320, 20µl
+!P613, 20µl
+|-
+!Fragment size
+| -
+|650 bp
+|170 bp
+|2100 bp
+|4000 bp
+|-
+|}
+<br/>
+[[Image:Freiburg10 p146,p268,p320,p613.jpg|400px|]]
+<br/>
+'''Gel extraction''': <br>
+{| border="1"
+|
+!pSB1C3_CMV (p146)
+!pSB1C3_ZEGFR:1907 (p268)
+!pSB1C3_001_bla (p320)
+!pSB1C3_001_Vp2/3_HSPG-Ko (p613)
+|-
+!DNA-concentration [ng/µl]
+|28,2
+|13,2
+|22,1
+|43,2
+|-
+|}
+<br>
+'''T4 Ligation pSB1C3_001_CMV''': <br>
+Volume vector p320: 4,63 µl <br>
+Volume insert p146: 3,37 µl <br>
+<br>
+<br>
+'''T4 Ligation pSB1C3_001_Vp2/3_HSPG-Ko_CMV_ZEGFR:1907''': <br>
+Volume vector p613:  2,9 µl <br>
+Volume insert p268:  3 µl <br>
+Volume insert p146:  3 µl <br>
+<br>
+'''Transformation''': <br>
+Was performed in BL21 according the standard protocol <br>
+====<p style="font-size:15px; background-color:#66bbff;"><b>CD assembly with new suffix primer</b></p>====
+'''Investigator: Kira'''
+*PCR program:
+<br />
+{| border="1"
+| components   || align="right" |volume in µl  || align="right" |volume in µl
+|-
+| 5x Phusion HF buffer  ||  align="right" | 10|| align="right" |10
+|-
+| 10 mM dNTP mix ||  align="right" |1||  align="right" |1
+|-
+| 0158 primer_for (1:10 dilution)||  align="right" |  2,5||  align="right" | 2,5
+|-
+|0159 primer_rev (1:10 dilution)||  align="right" | 2,5||  align="right" | 2,5
+|-
+|DNA template (1:100)||  align="right" |  0,5||  align="right" | 0,5
+|-
+|DMSO||  align="right" |  0||  align="right" | 0.5
+|-
+|Phusion polymerase||  align="right" | 0,5||  align="right" | 0,5
+|-
+|H<sub>2</sub>O||  align="right" | 33||  align="right" | 32,5
+|-
+|'''Total volume (e.g. 50 µl)'''||  align="right" | 50||  align="right" | 50
+|}
+<br />
+{| border="1"
+|Cycles||Temperature||Time
+|-
+|||98°C||1
+|-
+|10x||98°C||15"
+|-
+|||60°C||25"
+|-
+|||72°C||40"
+|-
+|20x||98°C||15"
+|-
+|||65°C||25"
+|-
+|||72°C||40"
+|-
+|1x||72°C||5'
+|-
+|Hold 4°C
+|}
+<br>
+no PCR bands are visible on the gel..--> PCR reaction failed.<br />
+====<p style="font-size:15px; background-color:#66bbFF;"><b>test digestion of all CD constructs</b></p>====
+<b>Investigator: Kira</b>
+'''Comment''': Because the PCR failed also with new suffix primer, we decided to check if the DNA samples are ok. 3 different CD samples were used as DNA samples.<br />
+_original CD with iGEM binding sites p(223)<br />
+_CD with SDM of PstI <br />
+_CD with SDM of PstI and NgoMIV (p290) <br />
+{| border="1"
+| components   || align="right" |volume in µl
+|-
+| DNA  ||  align="right" | 3
+|-
+| BSA 10x ||  align="right" |2,0
+|-
+| Buffer 4||  align="right" |  2,0
+|-
+|PstI-HF||  align="right" | 0,5
+|-
+|NgoMIV||  align="right" | 1,0
+|-
+|H<sub>2</sub>O||  align="right" | 11,5
+|-
+|'''Total volume (e.g. 20 µl)'''||  align="right" | 20
+|}
+<br />
+[[Image: Freiburg10_testdigestion 2010_09_28.jpg]]
+====<p style="font-size:15px; background-color:#66bbff;">'''Cloning of pSB1C3_Affibody_middlelinker_EGFP_His'''</p>====
+'''Investigator: Jessica''' <br>
+<b>Comment: There was a mistake in cloning pSB1C3_Affibody_middlelinker_EGFP_His so there is just pSB1C3_EGFP_His. in this plasmid will be cloned Affibody_middlelinker_EGFP_His</b> <br/>
+*Vector: name: pSB1C3_EGFP_His  '''P565'''
+*Insert: name: pBAD_Affibody_middlelinker_EGFP_His '''P596'''
+*new vector name: pSb1C3_ZEGFR:1907_middlelinker_EGFP_His '''P'''
+*buffer used: 4
+*DNA concentration (vector): 252,7 ng/µl; DNA concentration (insert): 101,4 µg/µl
+<br />
+{| border="1"
+| '''components'''   || align="right" |'''volume of pBAD  /µl'''  || align="right" |'''volume of pSB1C3 /µl'''
+|-
+| DNA  ||  align="right" |15 ||  align="right" |4
+|-
+| BSA (10x) ||  align="right" |2 ||  align="right" | 2
+|-
+| Buffer 4 (10x)||  align="right" |2||  align="right" |2
+|-
+|Enzyme XbaI||  align="right" |0,8 ||  align="right" |0,8
+|-
+|Enzyme AgeI||  align="right" |0,8 ||  align="right" |0,8
+|-
+|H2O||  align="right" |-||  align="right" |10,4
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 20,6||  align="right" |20
+|}
+<br />
+,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 120 Volt
+<br />
+<br />
+{| border="1"
+|
+!Marker
+!P565, 20µl
+!P596, 20µl
+|-
+!Sample
+|
+|
+|
+|-
+!Fragment size
+|
+|2100 bp
+|1000 bp
+|-
+|}
+<br/>
+[[Image:Freiburg10_Cloning of PSB1C3_pBad_Affibody_middlelinker_EGFP_His3.jpg|400px|]]
+<br/>
+'''Gel extraction''': <br>
+{| border="1"
+|
+!pSB1C3
+!Affibody_middlelinker_EFGP_His
+|-
+!DNA-concentration [ng/µl]
+|17,5
+|14,2
+|-
+|}
+<br>
+'''T4 Ligation''': <br>
+Volume vector:  2,9 µl <br>
+Volume insert:  5,1 µl <br>
+<br>
+'''Transformation''': <br>
+BL21 cells were used
+====<p style="font-size:15px; background-color:#66bbff;"><b>Sequencing analysis of pSB1C3_001_RC_IRCK, pSB1C3_001_RC_IRCK_VP1-ko_P5tataless and pSB1C3_001_RC_IRCK_VP2-ko_P5tataless</b></p>====
+<b>Investigator: Stefan </b><br>
+<p style="font-size:13px; color:red;">Because all these constructs were cloned via PCR out of the pAAV vector, a complete sequencing was performed:</p>
+<b>P548	pSB1C3_001_RC_InsRepCap_KpnIback_VP1-ko_P5tataless clone 1:</b><br>
+Sequence could be verified, can be used for further cloning steps!<br>
+<br>
+<b>P568	pSB1C3_001_RC_InsRepCap_KpnIback_VP2-KO_P5tataless clone 2:</b><br>
+Sequence could be verified, can be used for further cloning steps!<br>
+<br>
+<b>P594	pSB1C3_001_RC_InsRepCap_KpnIback_RFC10  clone 1:</b><br>
+Sequence could be verified, can be used for further cloning steps!<br>
+<br>
+====<p style="font-size:15px; background-color:#66bbff;"><b>Cloning of HSPG_KO_empty into pSB1C3_001_RC_IRCK_VP1-ko_P5tataless and pSB1C3_001_RC_IRCK_VP2-ko_P5tataless</b></p>====
+<b>Investigator: Stefan </b><br>
+<p style="font-size:13px; color:red;"></p>
+Vector name:
+<ul>
+<li>pSB1C3_001_RC_IRCK_VP1-ko_P5tataless (P548)</li>
+<li>pSB1C3_001_RC_IRCK_VP1-ko_P5tataless (P568)</li>
+Insert name:
+<li>VB:pSB1C3_001_KO_empty(P611)</li>
+</ul>
+<br />
+{| border="1"
+| '''components'''   || align="right" |'''volume of P548  /µl''' || align="right" |'''volume of P568 /µl'''  || align="right" |'''volume of P611 /µl'''
+|-
+| DNA  ||  align="right" |3,5 ||  align="right" |3,5  ||  align="right" |16
+|-
+| BSA (10x) ||  align="right" |2 ||  align="right" | 2 ||  align="right" | 3
+|-
+| Buffer 4 (10x)||  align="right" |2||  align="right" |2  ||  align="right" | 3
+|-
+|Enzyme BamHI||  align="right" |1 ||  align="right" |1 ||  align="right" |1
+|-
+|Enzyme PvuII||  align="right" |1 ||  align="right" |1 ||  align="right" |1
+|-
+|H2O||  align="right" |10,5||  align="right" |10,5||  align="right" |6
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 20||  align="right" |20 ||  align="right" |30
+|}
+<br />
+<b>Gel:</b><br />
+for vector:<br />
+,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 115 Volt<br />
+<br />
+for insert:<br />
+g Agarose, 50 ml TAE (2%), 3 µl GELRED , at 105 Volt<br />[[Image: Freiburg10_LabFun_28.09.2010.png|thumb|right|400px]]
+<br/>
+[[Image:Freiburg10 digestion of pSB1C3 VP1 VP2 ko HSPG ko.jpg|450px|]]<br/>
+<br/>
+<b>Gel extraction</b>: <br>
+Was performed according to protocol.
+<br>
+<b>T4 Ligation</b>: <br>
+<b>VP1-ko:</b><br>
+<ul>
+<li>Volume VP1-ko:  5,57 µl</li>
+<li>Volume insert:  2,43 µl</li>
+</ul>
+<b>VP2-ko</b><br>
+<ul>
+<li>Volume VP2-ko:  5,04 µl</li>
+<li>Volume insert:  2,96 µl</li>
+</ul>
+<br>
+<b>Transformation</b>: <br>
+Was performed according to standard protocol using BL21 cells.
+====<p style="font-size:15px; background-color:#66bbff;">'''Cloning of 587_KO_Z34C and 587_KO_Z34C_Spacer into pSB1C3_001_CMV_VP123_capins'''</p>====
+'''Investigator: Anna''' <br>
+<p style="font-size:13px; color:red;">Comment: Todays sequencing results of 587_KO_Z34C and 587_KO_Z34C_Spacer looked well, so they will be cloned into pSB1C3_CMV_VP123_capins. Finally produced ViralBricks:</p>
+[[media:Freiburg10_Production of ViralBricks_End version.pdf]]<br />
+*Vector name: pSB1C3_CMV_VP123_capins  '''P580'''
+*Insert name:
+. pSB1C3_587_KO_Z34C '''P599'''<br/>
+. pSB1C3_587_KO_Z34C_Spacer '''P600'''
+*buffer used: 4
+*DNA concentration (P580): 377,29 ng/µl;
+*DNA concentration (P599): 102,5 µg/µl
+*DNA concentration (P600): 90,4 µg/µl
+<br />
+{| border="1"
+| '''components'''   || align="right" |'''volume of P580  /µl''' || align="right" |'''volume of P599 /µl'''  || align="right" |'''volume of P600 /µl'''
+|-
+| DNA  ||  align="right" |2,7 ||  align="right" |14,7  ||  align="right" |16,7
+|-
+| BSA (10x) ||  align="right" |2,5 ||  align="right" | 2,5 ||  align="right" | 2,5
+|-
+| Buffer 4 (10x)||  align="right" |2,5||  align="right" |2,5  ||  align="right" | 2,5
+|-
+|Enzyme BamHI||  align="right" |1 ||  align="right" |1 ||  align="right" |1
+|-
+|Enzyme PvuII||  align="right" |1 ||  align="right" |1 ||  align="right" |1
+|-
+|H2O||  align="right" |15,3||  align="right" |3,3||  align="right" |1,3
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 25||  align="right" |25 ||  align="right" |25
+|}
+<br />
+,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 120 Volt
+<br />
+<br />
+{| border="1"
+|
+!Marker, 4 µl
+!P580
+!2: P599
+!3: P600
+|-
+!Construct
+|
+|pSB1C3_CMV_VP123_cut
+|587_KO_Z34C
+|587_KO_Z34C_Spacer
+|-
+|-
+!Fragment size
+|
+|5000 bp
+|194 bp
+|209 bp
+|-
+|}
+<br/>
+[[Image:Freiburg10_Digestion of p580.jpg|350px|]]
+[[Image:Freiburg10_Cloning of 587_KO_Z34C into pSB1C3_CMV_VP123_capins.jpg|350px|]]
+<br/>
+'''Gel extraction''': <br>
+Was performed following the standard protocol.
+<br>
+DNA-concentrations [ng/µl]:
+c(vector)= 18,88<br>
+c(587_KO_Z34C)= 9,74<br>
+c(587_KO_Z34C_Spacer)= 1,72<br>
+<br>
+'''T4 Ligation''': <br>
+_KO_Z34C:<br>
+Volume vector:  1,5 µl <br>
+Volume insert:  6,5 µl <br>
+_KO_Z34C_Spacer:<br>
+Volume vector:  4,6 µl <br>
+Volume insert:  3,4 µl <br>
+<br>
+'''Trafo''': <br>
+Was performed following the standard protocol using BL21 cells.
+<br/>
+====<p style="font-size:15px; background-color:#66bbff;">'''Mini-Prep and Test-digestion of VP1 insertion and VP2 fusion HSPG-KO approaches'''</p>====
+'''Investigator: Hanna''' <br>
+<br/>
+<b>Comments:</b> Yesterday, 2 clones of each construct were picked. Today mini-prep and test digestion will be performed of one of each approach - the other clones will be spinned down and stored at -20°C - waiting for test digestion and sequencing results. <br/>
+<br/>
+Mini-Prep was performed, following the standard protocol. <br/>
+<br/>
+<b>New plasmid names:</b> <br/>
+P617: pCerulean_CFP_MiddleLinker_VP2/3_HSPG-KO <br/>
+P618: pCerulean_ZEGFR:1907_MiddleLinker_VP2/3_HSPG-KO <br/>
+P619: pCerulean_ZEGFR:1907_SEG_VP2/3_HSPG-KO <br/>
+P620: pCerulean_ZEGFR:1907_ShortLinker_VP2/3_HSPG-KO <br/>
+P621: pCerulean_ZEGFR:1907_LongLinker_VP2/3_HSPG-KO <br/>
+P622: pCerulean_6xHis_MiddleLinker_VP2/3_HSPG-KO <br/>
+P623: pCerulean_VP1up_NLS_ZEGFR:1907_VP2/3_HSPG-KO <br/>
+P624: pCerulean_VP1up_NLS_6xHis_VP2/3_HSPG-KO <br/>
+P625: pCerulean_VP1up_NLS_mVenus_VP2/3_HSPG-KO <br/>
+<br/>
+<b>TEST DIGESTION:</b> <br/>
+Mastermix: <br/>
+* BSA (10x): 10 µL
+* Buffer 4: 10 µL
+* EcoRI: 5 µL
+* PstI: 5 µL
+* H<sub>2</sub>O: 37 µL
+<br/>
+DNA: 3.3 µL + 6.7 µL Master Mix.
+[[Image:Freiburg10 TestDigestionHSPGKO.png|500px|thumb|center]]
+<br/>
+<b>Conclusion:</b> Test digestion looked well - except of P618: There is an additional band visible, which can't be correlated to any construct. <br/>
+All samples were sent for sequencing. <br/>
+===<p style="font-size:17px; background-color:#00dd77;">134. labday 29.09.2010</p>===
+====<p style="font-size:15px; background-color:#66bbff;"><b>CD assembly with new suffix primer</b></p>====
+'''Investigator: Kira'''
+*PCR program:
+<br />
+as DNA samples p291 and p292 with and wo DMSO were used. <br />
+{| border="1"
+| components   || align="right" |volume in µl  || align="right" |volume in µl
+|-
+| 5x Phusion HF buffer  ||  align="right" | 10|| align="right" |10
+|-
+| 10 mM dNTP mix ||  align="right" |1||  align="right" |1
+|-
+| 0158 primer_for (1:10 dilution)||  align="right" |  2,5||  align="right" | 2,5
+|-
+|0159 primer_rev (1:10 dilution)||  align="right" | 2,5||  align="right" | 2,5
+|-
+|DNA template (1:100)||  align="right" |  0,5||  align="right" | 0,5
+|-
+|DMSO||  align="right" |  0||  align="right" | 0.5
+|-
+|Phusion polymerase||  align="right" | 0,5||  align="right" | 0,5
+|-
+|H<sub>2</sub>O||  align="right" | 33||  align="right" | 32,5
+|-
+|'''Total volume (e.g. 50 µl)'''||  align="right" | 50||  align="right" | 50
+|}
+<br />
+{| border="1"
+|Cycles||Temperature||Time
+|-
+|||98°C||1
+|-
+|10x||98°C||15"
+|-
+|||60°C||25"
+|-
+|||72°C||40"
+|-
+|20x||98°C||15"
+|-
+|||65°C||25"
+|-
+|||72°C||40"
+|-
+|1x||72°C||5'
+|-
+|Hold 4°C
+|}
+<br>
+[[Image: Freiburg10_CDPCR_2010_09_28.jpg]]
+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 (10x) ||align="left"| 2 µl
+|-
+| align="left" | Buffer no. 4 (10x) ||align="left"| 2,0 µl
+|-
+| align="left" | Enzyme 1 XbaI ||align="left"| 1,0 µl
+|-
+| align="left" | Enzyme 2 AgeI  ||align="left"| 1,5 µl
+|-
+| align="left" | H<sub>2</sub>O ||align="left"| 7,5 µl
+|-
+| align="left" | '''Total volume''' ||align="left"| <b>20</b>
+|}
+<br />
+incubation @ 37 C for approx. 2 h
+% agarose gel <br />
+Digestion of PCR product:
+{| border="1"
+| align="left" | '''Components''' ||align="left"| <b>PCR product</b> Volume/µL
+|-
+| align="left" | DNA   ||align="left"| 30,0 µl
+|-
+| align="left" | BSA (100x) ||align="left"| 0,4 µl
+|-
+| align="left" | Buffer no. 4  ||align="left"| 4,0 µl
+|-
+| align="left" | Enzyme 1 XbaI ||align="left"| 1,5 µl
+|-
+| align="left" | Enzyme 2 AgeI  ||align="left"| 2,0 µl
+|-
+| align="left" | H<sub>2</sub>O ||align="left"| 2,1 µl
+|-
+| align="left" | '''Total volume''' ||align="left"| <b>40</b>
+|}
+<br />
+incubation @ 37 C for approx. 2 h <br />
+ligation with T4 ligase: <br />
+c(insert)= 31,35 ng/ul <br />
+c(vector)= 10,45 ng/ul <br />
+ul DNA mix = insert 3 ul + vector 5 ul <br />
+T4 ligase 1 ul <br />
+T4 buffer 1 ul <br />
+Transformation: Anna
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Miniprep of serveral constructs</b></p>====
+<b>Investigator: Stefan</b>
+<b>Glycerol stocks were prepared:</b><br />
+<ul>
+<li>B516 =	pSB1C3_001_RC_ICRK_P5tataless_RFC10  clone 1</li>
+<li>B517 =	pSB1C3_pTAV (P5)</li>
+<li>B518 =	pSB1C3_001_RC_ICRK_P5tataless_RFC10  clone 2</li>
+</ul>
+<br />
+<br />
+<b>Mini-Prep was performed according to the standard protocol</b><br />
+<br />
+<ul>
+<li>P628 =	pSB1C3_001_RC_ICRK_P5tataless_RFC10  clone 1</li>
+<li>P629 =	pSB1C3_pTAV (P5)</li>
+<li>P630 =	pSB1C3_001_RC_ICRK_P5tataless_RFC10  clone 2</li>
+</ul><br />
+<b>Test digestion:</b><br />
+{| border="1"
+| Components   || align="right" |Volume P628 + P630 /µl
+|-
+| DNA  ||  align="right" |3
+|-
+| BSA  ||  align="right" |1
+|-
+| Buffer 4 (10x)||  align="right" |1
+|-
+|Enzyme I ||  align="right" |0,4
+|-
+|Enzyme II  ||  align="right" |0,4
+|-
+|H<sub>2</sub>O||  align="right" |4,2
+|-
+|'''Total volume '''||  align="right" |10
+|}
+<br />
+<p style="font-size:13px; color:red;"><b>Comment</b>:First test digestion using XmaI and SpeI did not work out, thererfore, two different approaches using MngBI/PstI and SnaBI and PstI were performed. This verified successful cloning of P5tataless into the target vector.</p>
+[[Image:Freiburg10 test digestion pSB1C3 001 IRCK P5tataless.jpg|550px]]<br />
+<b>Sent for sequencing:</b><br />
+pSB1C3_001_RC_ICRK_P5tataless_RFC10 clone 1 (P628) was sent for sequencing using VR2 primer.
+====<p style="font-size:15px; background-color:#66bbFF;"><b>mGMK_TK30 approaches</b></p>====
+<b>Investigator: Bea</b>
+<br/>
+<p style="color:#66bbff;"><i>Comment</i>: Since we are still waiting for the TK30 gene ordered at Mr.Gene we decided to take another road to produce a BioBrick compatible thymidine kinase gene. Therefore, we are cloning the mGMK_TK30 fusion construct into the pSB1C3 and after removing the PstI site (see next topic) it is ready for submitting it to the parts registry.  Additionally, we are fusing the mGMK_TK30 to the composite part pSB1C3-leftITR_PROMOTER_betaglobin for testing it in cell culture with pur final super construct.</p>
+<br />
+<b>Digestion of the constructs:</b>
+<ul>
+<li>P51.2 = pSB1C3_CFP </li>
+<li>P81 = pAAV_RFC25_mGMK_TK30</li>
+<li>P434 = pSB1C3_leftITR_CMV_betaglobin</li>
+<li>P437 = pSB1C3_leftITR_phTERT_betaglobin</li>
+</ul>
+<br />
+{| border="1"
+| align="left" | '''Components''' ||align="left"| <b>v<sub>P51.2</sub> /µL</b> ||align="left"| <b>v<sub>P81 upstream</sub>/µL</b> ||align="left"| <b>v<sub>P81</sub> /µL</b> ||align="left"| <b>v<sub>P434</sub>/µL</b>  ||align="left"| <b>v<sub>P437</sub>/µL</b>
+|-
+| align="left" | DNA  ||align="left"| 5||align="left"|5 ||align="left"|10 ||align="left"|4,5||align="left"|4,5
+|-
+| align="left" | BSA (10x) ||align="left"| 2||align="left"|2 ||align="left"| 2||align="left"| 2||align="left"| 2
+|-
+| align="left" | Buffer no. 4 (10x) ||align="left"| 2||align="left"|2 ||align="left"| 2||align="left"| 2||align="left"| 2
+|-
+| align="left" | Enzyme 1 ||align="left"|EcoRI||align="left"|SpeI  ||align="left"|SpeI 1||align="left"|-||align="left"|-
+|-
+| align="left" | Enzyme 2 ||align="left"|SpeI||align="left"|XbaI||align="left"|EcoRI||align="left"|SpeI||align="left"|SpeI
+|-
+| align="left" | H<sub>2</sub>O ||align="left"|9||align="left"|9||align="left"|4||align="left"|10,5||align="left"|10,5
+|-
+| align="left" | '''Total volume''' ||align="left"| '''20''' ||align="left"| '''20''' ||align="left"| '''20''' ||align="left"| '''20'''||align="left"| '''20'''
+|-
+|}
+<br />
+<br />
+<b>Overview cloning plan:</b>
+<br />
+[[Image:Freiburg10 CloningPlan mGMK TK30.PNG|thumb|center|700px]]
+<br/>
+<br/>
+<b>Loading plan of a 0,8% agarose gel:</b>
+<br/>
+ M    P51.2    P81 (digested with E+S)    P81 (digested with X+S)    P434    P437
+<br/>
+<b>Expected sizes of the digested products are:</b>
+<ul>
+<li> pAAV_RFC25_mGMK_TK30= 4626, <b>1717bp</b></li>
+<li> pAAV_RFC25_mGMK_TK30= 4626, <b>1717bp</b></li>
+<li> pSB1C3_CFP = <b>2052</b>, 756bp</li>
+<li> pSB1C3_leftITR_CMV_betaglobin= <b>5094b</b></li>
+<li> pSB1C3_leftITR_phTERT_betaglobin= <b>5094b</b></li>
+</ul>
+<br />
+<b>Results:</b>
+[[Image: Freiburg10_mGMK_TK30_several_approaches_29.09.2010.png|thumb|center|500px]]
+<br />
+<br />
+After Gel extraction have been performed the ligation was conducetd:
+<br />
+[[Image:Freiburg10 mGMK TK30 ligation 29.09.2010.png|thumb|center|700px]]
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Design of mutagenesis primers for deletion of PstI in mGMK_TK30</b></p>====
+<b>Investigator: Bea</b>
+<br/>
+<p style="color:#66bbff;"><i>Comment</i>: Since we are still waiting for the TK30 gene ordered at Mr.Gene we decided to take another road to produce a BioBrick compatible thymidine kinase gene. Therefore, new primers were designed in order to remove the PstI restriction sites within the TK30 gene. The primers will be ordered tomorrow. </p>
+<br />
+<br />
+[[Image: Freiburg10_PrimerDesign_TK30_SDM_PstI_29.09.2010.PNG|thumb|center|700px]]
+====<p style="font-size:15px; background-color:#66bbff;"><b>Cloning of Darpin into pCerulean_Vp1up_NLS and pSB1C3 Part Two </b></p>====
+'''Investigator: Achim'''
+*I accidentally plated yesterdays trafo with the wrong antibiotics and I had to digest pSB1C3 again anyway, so I prepared a new digestion of both vectors with Age & Spe.
+[[Image:Freiburg10 29.9 darpin.png|none|thumb|150px]]
+* After watching the gel picture I realized I had digested pSB1C3 with the wrong enzymes. I should have used NgOMIV and Spe in order to cut out BLA.
+*pCerulean_Vp1up_NLS was ligated with yesterdays Darpin fragment and plated on Ampicillin, the pSB1C3_BLA construct will be cloned correctly tomorrow
+====<p style="font-size:15px; background-color:#66bbff;">'''Cloning of pGGTBT7_Affibody_middlelinker_EGFP_His'''</p>====
+'''Investigator: Jessica''' <br>
+<b>Comment: pBAD is not really working, so we test another expression-plasmid</b> <br/>
+*Vector: name: pGGTBT7_MVenus  '''P627'''
+*Insert: name: pBAD_Affibody_middlelinker_EGFP_His '''596'''prepared yesterday
+*new vector name: pGGTBT7_ZEGFR:1907_middlelinker_EGFP_His '''P'''
+*buffer used: 4
+*DNA concentration (vector): 144,1 ng/µl; DNA concentration (insert): 101,4 µg/µl
+<br />
+{| border="1"
+| '''components'''   || align="right" |'''volume of pBAD  /µl'''
+|-
+| DNA  ||  align="right" |10
+|-
+| BSA (10x) ||  align="right" |2
+|-
+| Buffer 4 (10x)||  align="right" |2
+|-
+|Enzyme XbaI||  align="right" |0,8
+|-
+|Enzyme AgeI||  align="right" |0,8
+|-
+|H2O||  align="right" |4,4
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 20
+|}
+<br />
+,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 120 Volt
+<br />
+<br />
+{| border="1"
+|-
+!Fragment size
+|
+|5200 bp
+|730 bp
+|-
+|}
+<br/>
+[[Image:Freiburg10_Cloning of pGGTBT7_Affibody_middlelinker_EGFP_His.jpg|100px|]]
+<br/>
+'''Gel extraction''': <br>
+{| border="1"
+|
+!pGGTBT7
+!Affibody_middlelinker_EFGP_His
+|-
+!DNA-concentration [ng/µl]
+|20,79
+|7,84
+|-
+|}
+<br>
+'''T4 Ligation''': <br>
+Volume vector: 3,2  µl <br>
+Volume insert: 4,8  µl <br>
+<br>
+'''Transformation''': <br>
+BL21 DE3 R2L(Kana+Cm), BL21 DE3(Kana), BL21DE3 R2(Kana+Cm) cells were used
+====<p style="font-size:15px; background-color:#66bbff;">'''Cloning of CMV promotor and Affibody into pSB1C3_001_VP2/3_capins and pSB1C3_001_VP2/3_HSPG_KO '''</p>====
+'''Investigator: Anna''' <br>
+<p style="font-size:13px; color:red;">Comment: Cloning of CMV promotor and Affibody into pSB1C3_001_VP2/3_HSPG_KO was repeated, because it was not clear if the first attempt worked. </p>
+*Vector name:
+. pSB1C3_001_VP2/3_capins '''P514''': 318,9 ng/µl<br/>
+. pSB1C3_001_VP2/3_HSPG_KO '''P613''': 273,6 ng/µl<br/>
+*Insert name:
+. pSB1C3_CMV '''P146''': 155,6 ng/µl<br/>
+. pSB1C3_ZEGFR:1907 '''P248''': 146,5 ng/µl<br/>
+*buffer used: 4
+<br />
+{| border="1"
+| '''components'''   || align="right" |'''volume of P514 /µl''' || align="right" |'''volume of P613 /µl'''  || align="right" |'''volume of P146 /µl''' || align="right" |'''volume of P248 /µl'''
+|-
+| DNA  ||  align="right" |3,1 ||  align="right" |3,7  ||  align="right" |12,8 ||  align="right" |13,7
+|-
+| BSA (10x) ||  align="right" |2,0 ||  align="right" | 2,0  ||  align="right" | 2,0 ||  align="right" |2,0
+|-
+| Buffer 4 (10x)||  align="right" |2,0 ||  align="right" |2,0   ||  align="right" |2,0 ||  align="right" |2,0
+|-
+|Enzyme I||  align="right" |EcoRI  1 ||  align="right" |EcoRI   1 ||  align="right" |XbaI  1||  align="right" |SpeI  1
+|-
+|Enzyme II||  align="right" |NgoMIV 1 ||  align="right" |NgoMIV  1 ||  align="right" |AgeI  1||  align="right" |EcoRI  1
+|-
+|H2O||  align="right" |10,9||  align="right" |10,3||  align="right" |1,2||  align="right" |0,3
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 20||  align="right" |20 ||  align="right" |20||  align="right" |20
+|}
+<br />
+,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 120 Volt
+<br />
+<br />
+{| border="1"
+|
+!Marker, 4 µl
+!Vector 1: pSB1C3_001_VP2/3_capins
+!Vector 2: pSB1C3_001_VP2/3_HSPG_KO
+!CMV
+!Affibody
+|-
+!Fragment size
+|
+|4000 bp
+|4000 bp
+|650 bp
+|170 bp
+|-
+|}
+<br/>
+[[Image:Freiburg10_3 Fragment ligation of affibody and CMV.jpg|350px|]]
+<br/>
+'''Gel extraction''': <br>
+Was performed following the standard protocol.
+<br>
+DNA-concentrations [ng/µl]:
+c (pSB1C3_001_VP2/3_capins) = 40.9 <br>
+c (pSB1C3_001_VP2/3_HSPG_KO)= 51.94<br>
+c (CMV)= 12.67<br>
+c (Affibody)= 14.44<br>
+<br>
+'''T4 Ligation''': <br>
+*Vector 1:<br>
+Volume vector:  2,8 µl <br>
+Volume Affibody:  2,0 µl <br>
+Volume CMV:  3,2 µl <br>
+*Vector 2:<br>
+Volume vector:  2,5 µl <br>
+Volume Affibody:  2,0 µl <br>
+Volume CMV:  3,5 µl <br>
+<br>
+'''Trafo''': <br>
+Was performed following the standard protocol using BL21 cells.
+====<p style="font-size:15px; background-color:#66bbff;">'''Cloning of CFP into pSB1C3_lITR_phTERT_beta-globin '''</p>====
+'''Investigator: Anissa''' <br>
+*Vector name:
+pSB1C3_lITR_phTERT_beta-globin '''P514''': 333,46 ng/µl<br/>
+*Insert name:
+pSB1C3_CFP '''P146''': 151,1 ng/µl<br/>
+*buffer used: 4
+<br />
+{| border="1"
+| '''components'''   || align="right" |'''volume of P51.2 /µl''' || align="right" |'''volume of P437 /µl'''
+|-
+| DNA  ||  align="right" |13,2||  align="right" |4,5
+|-
+| BSA (10x) ||  align="right" |2,0 ||  align="right" | 1,5
+|-
+| Buffer 4 (10x)||  align="right" |2,0 ||  align="right" |1,5
+|-
+|Enzyme I||  align="right" |XbaI 1 ||  align="right" |SpeI 1
+|-
+|Enzyme II||  align="right" |PstI 1 ||  align="right" |PstI 1
+|-
+|H2O||  align="right" |0,8||  align="right" |5,5
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 20||  align="right" |15
+|}
+<br />
+,5 g Agarose, 50 ml TAE (1%), 1,5 µl GELRED , at 115 Volt
+<br />
+<br />
+{| border="1"
+|
+!Marker, 4 µl
+!Vector
+!Insert
+|-
+!Fragment size
+|
+|3180 bp
+|750 bp
+|-
+|}
+<br/>
+[[Image:Freiburg10 p51.2,p437.jpg|350px|]]
+'''Gel extraction''': <br>
+Was performed following the standard protocol.
+<br>
+DNA-concentrations [ng/µl]:
+c (pSB1C3_CFP) = 11,6 <br>
+c (pSB1C3_lITR_phTERT_beta-globin)= 24,8 <br>
+<br>
+'''T4 Ligation''': <br>
+*Volume vector:  3,2 µl <br>
+*Volume insert:  4,8 µl <br>
+'''Trafo''': <br>
+Was performed following the standard protocol using BL21 cells.
+<br/>
+====<p style="font-size:15px; background-color:#66bbff;">'''Sequencing results: VP1 insertion and VP2 fusion: Fusion of VP2/3_HSPG-KO '''</p>====
+'''Investigator: Hanna''' <br>
+<br/>
+<gallery caption="Sample gallery" widths="430px" heights="300px" perrow="2">
+Image:Freiburg10 29 9Seq1.png|pCerulean_CFP_MiddleLinker_ VP2/3_HSPG-KO (P617)
+Image:Freiburg10 29 9Seq7.png|pCerulean_Z<sub>EGFR:1907</sub>_MiddleLinker_ VP2/3_HSPG-KO (P618)
+Image:Freiburg10 29 9Seq3.png|pCerulean_Z<sub>EGFR:1907</sub>_SEG_ VP2/3_HSPG-KO (P619)
+Image:Freiburg10 29 9Seq2.png|pCerulean_Z<sub>EGFR:1907</sub>_ShortLinker_ VP2/3_HSPG-KO (P620)
+Image:Freiburg10 29 9Seq4.png|pCerulean_Z<sub>EGFR:1907</sub>_LongLinker_ VP2/3_HSPG-KO (P621)
+Image:Freiburg10 29 9Seq5.png|pCerulean_6xHis</sub>_MiddleLinker_ VP2/3_HSPG-KO (P622)
+Image:Freiburg10 29 9Seq6.png|pCerulean__VP1up_NLS_Z<sub>EGFR:1907</sub>_ VP2/3_HSPG-KO (P623)
+Image:Freiburg10 29 9Seq8.png|pCerulean_VP1up_NLS_6xHis_ VP2/3_HSPG-KO (P624)
+Image:Freiburg10 29 9Seq9.png|pCerulean_VP1up_NLS_mVenus_ VP2/3_HSPG-KO (P625)
+</gallery>
+<br/>
+<b>Conclusion:</b> Except of pCerulean_Z<sub>EGFR:1907</sub>_MiddleLinker_ VP2/3_HSPG-KO (P618), all sequencing results looked well. This means: The VP2/3-HSPG-KO motif was cloned successfully to the VP2-Fusion and VP1-Insertion approaches and are ready to be tested in cell culture via qPCR and ELISA. --> Co-transfection with pSB1C3_001_RC_iRCK_VP1or2-KO_HSPG-KO + pHelper + pSB1C3_GOI. <br/>
+<br/>
+In addition to that, clone 2 of pCerulean_Z<sub>EGFR:1907</sub>_MiddleLinker_ VP2/3_HSPG-KO will be preped and test digested tomorrow.
+<br/>
+====<p style="font-size:15px; background-color:#66bbff;"><b>Cloning of HSPG_KO_empty into pSB1C3_001_RC_IRCK_P5tataless</b></p>====
+<b>Investigator: Stefan </b><br>
+<p style="font-size:13px; color:red;"></p>
+Vector name:
+<ul>
+<li>pSB1C3_001_RC_IRCK_P5tataless cl1 (P628)</li>
+<li>pSB1C3_001_RC_IRCK_P5tataless cl2 (P630)</li>
+Insert name:
+<li>VB:pSB1C3_001_KO_empty(P611)</li>
+</ul>
+<br />
+{| border="1"
+| '''components'''   || align="right" |'''volume of P628  /µl'''|| align="right" |'''volume of P630  /µl''' || align="right" |'''volume of P611 /µl'''
+|-
+| DNA  ||  align="right" |3,5 ||  align="right" |3,5||  align="right" |16
+|-
+| BSA (10x) ||  align="right" |2 ||  align="right" |2||  align="right" | 3
+|-
+| Buffer 4 (10x)||  align="right" |2 ||  align="right" |2 ||  align="right" | 3
+|-
+|Enzyme BamHI||  align="right" |1||  align="right" |1 ||  align="right" |1
+|-
+|Enzyme PvuII||  align="right" |1||  align="right" |1 ||  align="right" |1
+|-
+|H2O||  align="right" |10,5||  align="right" |10,5||  align="right" |6
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 20||  align="right" | 20||  align="right" |30
+|}
+<br />
+<b>Gel:</b><br />
+for vector:<br />
+,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 110 Volt<br />
+<br />
+for insert:<br />
+g Agarose, 50 ml TAE (2%), 3 µl GELRED , at 110 Volt<br />
+<br/>
+[[Image:Freiburg10 digestion of pSB1C3 RFC10 HSPG ko.jpg|450px|]]<br/>
+<br/>
+<b>Gel extraction</b>: <br>
+Was performed according to protocol.
+<br>
+<b>T4 Ligation</b>: <br>
+<ul>
+<li>Volume vector P628:  7,11 µl</li>
+<li>Volume insert:  0,89 µl</li>
+</ul>
+<ul>
+<li>Volume vector P630:  7,33 µl</li>
+<li>Volume insert:  0,67 µl</li>
+</ul>
+<br>
+<b>Transformation</b>: <br>
+Was performed according to standard protocol using BL21 cells.
+====<p style="font-size:15px; background-color:#66bbff;">Mass Midi-Prep II </p>====
+'''Investigator: Chris W. <br>'''
+<p style="font-size:13px; color:#003399;"> Midi-Prep of:</p><br/>
+_BAP =P631<br/>
+_BAP =P632<br/>
+_KO_BAP =P633<br/>
+_RGD =P634<br/>
+_RGD =P635<br/>
+_KO_RGD =P636<br/>
+_HIS =P637<br/>
+_HIS =P638<br/>
+_KO_HIS =P639<br/>
+_KO_empty =P640<br/>
+_Z34C =P641<br/>
+pSB1C3_001_RC_IRCK_VP1-ko_P5tataless =P642 =B463<br/>
+pSB1C3_001_RC_IRCK_VP2-ko_P5tataless =P643 =B470<br/>
+<br/>
+The Midi-Preps were performed according to the standard protocol yielding the following concentrations:
+{| border="1"
+| plasmid-no. || align="right" |P631|| align="right" |P632|| align="right" |P633|| align="right" |P634|| align="right" |P635|| align="right" |P636|| align="right" |P637|| align="right" |P638|| align="right" |P639|| align="right" |P640|| align="right" |P641|| align="right" |P642|| align="right" |P643
+|-
+| concentration (ng/µl)|| align="right" |4758,69 || align="right" |448,12 || align="right" |3243,97|| align="right" |2231,44|| align="right" |1401,68|| align="right" |3289,15|| align="right" |3441,22|| align="right" |3058,92|| align="right" |4425,05|| align="right" |2339,06|| align="right" |4377,05|| align="right" |5045,55|| align="right" |5201,73
+|}
+<br>
+<br/>
+===<p style="font-size:17px; background-color:#00dd77;">135. labday 30.09.2010</p>===
+====<p style="font-size:15px; background-color:#66bbFF;"><b>picking CD clones</b></p>====
+<b>Investigator: Kira</b>
+The agaro plate contained many clones, 4 of them were picked and inoculated into media <br />
+====<p style="font-size:15px; background-color:#66bbFF;"><b>ViralBricks BAP-ko and His-ko in VP23</b></p>====
+<b>Investigator: Bea</b>
+<br/>
+<p style="color:#66bbff;"><i>Comment</i>: In order to verify the insertion of the ViralBricks BAP-ko and His-ko into the VP23 construct we digested the produced constructs with SalI and BamHI (both HF) and loaded it on a 1%a agarose gel. The constructs were used for creating the final super constructs (yay). Sequencing will verify if we subcloned the ViralBrick truly/seriously into the plasmids.</p>
+<br />
+<b>Digestion of the constructs:</b>
+<ul>
+<li>P660 = pSB1C3_001_VP2/3_HSPG-ko_587_BAP</li>
+<li>P661 = pSB1C3_001_VP2/3_HSPG-ko_587_BAP</li>
+<ul><b>Expected size: 464bp</b></ul>
+<li>P662 = pSB1C3_001_VP2/3_HSPG-ko_587_His</li>
+<li>P663 = pSB1C3_001_VP2/3_HSPG-ko_587_His</li>
+<ul><b>Expected size: 437bp</b></ul>
+<li>P525 = pSB1C3_001_VP2/3_capins</li>
+<ul><b>Expected size: 404bp</b></ul>
+</ul>
+<br />
+[[Image: Freiburg10_Testdigestion_BiralBricks_VP23_29.09.10.png|thumb|center|800px]]
+<br />
+<b>Results</b>:
+<br>
+The detected bands correspond to the expected sizes, but we cannot distinguish between the exact sizes because they are too similar. Therefore we sent P660 and P663 for sequencing in order to confirm if the ViralBricks have been successfully subcloned in the pSB1c3_VP2/3 construct.
+====<p style="font-size:15px; background-color:#66bbff;"><b>Cloning of Darpin into pCerulean_Vp1up_NLS and pSB1C3 Part Three </b></p>====
+<b>Investigator: Achim </b>
+*Clones of the pCerulean_Vp1up_NLS_Darpin construct were picked and will be prepped tonight.
+*pSB1C3_001_BLA (P320) and pMA_Darpin (P614) were digested with NgOMIV and SpeI. Bands were cut out accordingly, ligated with T4 ligase and plated on Chloramphenicol.
+<br/>
+[[image:Freiburg10_30.9._Darpin.png|thumb|none|300px]]
+====<p style="font-size:15px; background-color:#66bbff;">Test digestion of pCerulean_Z<sub>EGFR:1907</sub>_MiddleLinker_VP2/3_HSPG-KO clone 2</p>====
+'''Investigator: Hanna <br>'''
+<br/>
+<b>Comment:</b> Yesterday's sequencing results revealed, that VP2/3_HSPG-KO was successfully cloned to the VP2 fusion and VP1 insertion approaches, except of pCerulean_Z<sub>EGFR:1907</sub>_MiddleLinker_VP2/3_HSPG-KO clone 2. The chromatogram showed that fusion worked, but there was a kind of contamination in the sample - already visible in the test digestion. <br/>
+<br/>
+* DNA = 2 µL
+* BSA (10x) = 1 µL
+* Buffer 4 = 1 µl
+* EcoRI = 0.5 µL
+* PstI = 0.5 µL
+* H<sub>2</sub>0 = 5 µL
+<br/>
+Incubation time = 45 minutes. <br/>
+.9 % Agarose gel. <br/>
+<br/>
+[[Image:Test 30 Freiburg10 9.png|200px|thumb|center]] <br/>
+<br/>
+Test digestion looked well. Sample was sent for sequencing. <br/>
+====<p style="font-size:15px; background-color:#66bbff;">Cloning VP2/3_Capins and VP2/3_HSPG-KO downstream of Middle Linker</p>====
+'''Investigator: Hanna <br>'''
+<br/>
+<p style="color:#800080;"><b>Comment:</b> Besides the Affibody we also want to test and characterize the DARPin for its binding properties referring to the VP2 fusion and VP1 insertion. Therefore some preliminary cloning steps have to be performed. Today the VP2/3_insCap and VP2/3_HSPG-KO sequence will be cloned downstream of the Middle Linker for the VP2 fusion. </p>
+<br/>
+<p style="font-size:15px; font-weight: bold; color: #800080;">Practical Cloning:</p>
+**Vector: pGA14_MiddleLinker (P301)
+**Insert: pSB1C3_VP2/3_insCap (P525) and pSB1C3_001_VP2/3_HSPG-KO (P613)
+*new vector name: pGA14_MiddleLinker_VP2/3_insCap and pGA14_MiddleLinker_VP2/3_HSPG-KO
+*buffer used: 4 ; Restriction-enzymes used: PstI, AgeI/NgoMIV
+<br />
+<br />
+<p style="font-size:15px; font-weight: bold; color: #800080;">Digestion</p>
+{| border="1"
+| components   || align="right" |volume of P301 /µl || align="right" |volume of P525 /µl || align="right" |volume of P613 /µl
+|-
+| DNA  ||  align="right" | 5 ||  align="right" | 7.6 ||  align="right" | 5.5
+|-
+| BSA (10x) ||  align="right" | 2 ||  align="right" | 2 ||  align="right" | 2
+|-
+| Buffer 4 (10x)||  align="right" | 2 ||  align="right" | 2 ||  align="right" | 2
+|-
+|PstI ||  align="right" | 1 ||  align="right" | 1 ||  align="right" | 1
+|-
+|AgeI ||  align="right" | 1  ||  align="right" | - ||  align="right" | -
+|-
+|NgoMIV ||  align="right" | -  ||  align="right" | 1 ||  align="right" | 1
+|-
+|McsI ||  align="right" | 0.5  ||  align="right" | 0.5 ||  align="right" | 0.5
+|-
+|H<sub>2</sub>O||  align="right" | 9 ||  align="right" | 6.4 ||  align="right" | 8.5
+|-
+|'''Total volume'''||  align="right" | 20 ||  align="right" | 20 ||  align="right" | 20
+|}
+* Comment: After 30 minutes of digestion I remembered that it would be adventageous to digest the plasmid backbone of the VP2/3 constructs. Therefore 0.5 µL of McsI was added to each sample - fortunately McsI does not have any restriction sites in the pGA14_MiddleLinker to which it was also added by mistake. <br/>
+*Incubation: 20 minutes + 2 hours.
+<br /><br />
+<p style="font-size:15px; font-weight: bold; color: #800080;">Agarose-Gel:</p>
+<br />
+.5 g Agarose, 50 mL TAE (1 %), 3 µL GELRED, at 10 Volt, running time: 45 minutes
+<br />
+<br />
+{| border="1" cellspacing="0" cellpadding="2" bordercolor="black"
+!Sample
+!Sample/µl]
+!Loading dye (6x)/µl
+!Expected size 1
+!Expected size 2
+!Expected size 3
+|--
+|P301
+|20 µl
+|4 µl
+|~ 2450 bp
+|- bp
+|- bp
+|--
+|P525
+|20 µl
+|4 µl
+|1951 bp
+|738 bp
+|1324bp
+|--
+|P613
+|20 µl
+|4 µl
+|1951 bp
+|738 bp
+|1324bp
+|--
+|}
+{| align=right
+|}
+<br />
+*Marker: GeneRuler ladder mix
+{| border="1"
+|
+!Marker /µl
+!Sample P301 /µl
+!Sample P525 /µl
+!Sample P613 /µl
+|-
+!Lane
+|4.5
+|24
+|24
+|24
+|-
+|}
+<br />
+[[Image:Freiburg10_30_9_Cloning.png|500px|thumb|center]]
+<p style="font-size:15px; font-weight: bold; color: #800080;">Gel extraction</p>
+<br />
+Gel measurement:
+<br />
+{| border="1"
+| align="left" | '''Sample'''
+| align="left" | '''Weight'''
+| align="left" | '''Concentration'''
+|-
+| align="left" | P301
+| align="left" | 250 mg
+| align="left" | 38.41
+|-
+| align="left" | P525
+| align="left" | 270 mg
+| align="left" | 18.21
+|-
+| align="left" | P613
+| align="left" | 300 mg
+| align="left" | 21.55
+|}
+<br /><br />
+<p style="font-size:15px; font-weight: bold; color:#800080;">Ligation</p>
+<br />
+{| border="1"
+|'''Construct'''
+|'''Vector (µl)'''
+|'''Insert (µl)'''
+|'''T4 Ligase Buffer (µl)'''
+|'''T4 Ligase (µl)'''
+|-
+| pGA14_MiddleLinker_VP2/3_insCap
+| 1.32
+| 6.68
+| 1
+| 1
+|-
+| pGA14_MiddleLinker_VP2/3_HSPG-KO
+| 1.52
+| 6.48
+| 1
+| 1
+|-
+|}
+<br />
+====<p style="font-size:15px; background-color:#66bbFF;"><b>Miniprep of serveral constructs</b></p>====
+<b>Investigator: Jessica</b>
+<b>Glycerol stocks were prepared:</b><br />
+*B527	pSB1C3_001_CMV_VP2/3_587-KO_Z34C_spacer clone3
+*B528	pSB1C3_001_CMV_VP123_587-KO_Z34C clone1
+*B529	pSB1C3_001_CMV_VP123_587-KO_Z34C clone2
+*B530	pSB1C3_001_CMV_VP123_587-KO_Z34C clone3
+*B531	pSB1C3_oo1_CMV clone1
+*B532	pSB1C3_oo1_CMV clone2
+*B533	pSB1C3_001_CMV_ZEGFR:1907_VP2/3_HSPG-KO clone1
+*B534	pSB1C3_001_CMV_ZEGFR:1907_VP2/3_HSPG-KO clone2
+*B535	pSB1C3_001_VP2/3_ins_HSPG-KO_CMV_ZEGFR:1907 clone 1
+*B536	pSB1C3_001_VP2/3_ins_HSPG-KO_CMV_ZEGFR:1907 clone 2
+*B537	pBS1C3_001_VP2/3_587_BAP_HSPG-KO clone1
+*B538	pBS1C3_001_VP2/3_587_BAP_HSPG-KO clone2
+*B539	pBS1C3_VP2/3_capins_His clone1
+*B540	pBS1C3_VP2/3_capins_His clone2
+*B541	pSB1C3_ZEGFR:1907 _middlelinker_EGFP_His clone1
+*B542	pSB1C3_ZEGFR:1907 _middlelinker_EGFP_His clone2
+<br />
+<br />
+<b>Mini-Prep was performed according to the standard protocol</b><br />
+<br />
+*P644		pSB1C3_001_RC_IRCK_VP1-ko_HSPG-ko_P5tataless cl1 c= 151,0 ng/µl
+*P645		pSB1C3_001_RC_IRCK_VP1-ko_HSPG-ko_P5tataless cl2 c= 115,8 ng/µl
+*P646		pSB1C3_001_RC_IRCK_VP2-ko_HSPG-ko_P5tataless cl1 c= 173,1 ng/µl
+*P647		pSB1C3_001_RC_IRCK_VP2-ko_HSPG-ko_P5tataless cl2 c= 119,9 ng/µl
+*P648		pSB1C3_001_CMV_VP123_587-KO_Z34C_spacer clone1 c= 226,8 ng/µl
+*P649		pSB1C3_001_CMV_VP123_587-KO_Z34C_spacer clone2 c= 290,3 ng/µl
+*P650		pSB1C3_001_CMV_VP123_587-KO_Z34C_spacer clone3 c= 284,2 ng/µl
+*P651		pSB1C3_001_CMV_VP123_587-KO_Z34C clone1 c= 283,8 ng/µl
+*P652		pSB1C3_001_CMV_VP123_587-KO_Z34C clone2 c= 290,5 ng/µl
+*P653		pSB1C3_001_CMV_VP123_587-KO_Z34C clone3 c= 251,7 ng/µl
+*P654		pSB1C3_oo1_CMV clone1 c= 199,5 ng/µl
+*P655		pSB1C3_oo1_CMV clone2 c= 192,7 ng/µl
+*P656		pSB1C3_001_CMV_ZEGFR:1907_VP2/3_HSPG-KO clone1 c= 200,3 ng/µl
+*P657		pSB1C3_001_CMV_ZEGFR:1907_VP2/3_HSPG-KO clone2 c= 325,0 ng/µl
+*P658		pSB1C3_001_CMV_ZEGFR:1907_VP2/3_HSPG-KO clone3 c= 222,9 ng/µl
+*P659		pSB1C3_001_CMV_ZEGFR:1907_VP2/3_HSPG-KO clone4 c= 201,3 ng/µl
+*P660		pBS1C3_001_VP2/3_587_BAP_HSPG-KO clone1  c= 267,1 ng/µl
+*P661		pBS1C3_001_VP2/3_587_BAP_HSPG-KO clone2 c= 193,1 ng/µl
+*P662		pBS1C3_VP2/3_capins_His clone1 c= 209,1 ng/µl
+*P663		pBS1C3_VP2/3_capins_His clone2 c= 252,5 ng/µl
+*P664		pSB1C3_ZEGFR:1907 _middlelinker_EGFP_His clone1 c= 185,7 ng/µl
+*P665		pSB1C3_ZEGFR:1907 _middlelinker_EGFP_His clone2 c= 192,0 ng/µl
+*P666		pSB1C3_CFP c= 212,7  ng/µl
+====<p style="font-size:15px; background-color:#66bbff;">Test digestion of pSB1C3_ZEGFR:1907 _middlelinker_EGFP_His and mCherry iGEM 2008</p>====
+'''Investigator: Jessica <br>'''
+{| border="1"
+| components   || align="right" |volume of P664 pSB1C3_ZEGFR:1907 _middlelinker_EGFP_His /µl || align="right" |volume of P665 pSB1C3_ZEGFR:1907 _middlelinker_EGFP_His /µl || align="right" |volume of P626 mCherry /µl
+|-
+| DNA  ||  align="right" | 1,5 ||  align="right" | 1,5 ||  align="right" | 1,5
+|-
+| BSA (10x) ||  align="right" | 1 ||  align="right" | 1 ||  align="right" | 1
+|-
+| Buffer 4 (10x)||  align="right" | 1 ||  align="right" | 1 ||  align="right" | 1
+|-
+|XbaI ||  align="right" | 0,4 ||  align="right" | 0,4 ||  align="right" | 0,4
+|-
+|AgeI ||  align="right" | 0,4  ||  align="right" | 0,4 ||  align="right" | 0,4
+|-
+|H<sub>2</sub>O||  align="right" | 5,7 ||  align="right" | 5,7 ||  align="right" | 5,7
+|-
+|'''Total volume'''||  align="right" | 10 ||  align="right" | 10 ||  align="right" | 10
+|}
+<br/>
+<gallery caption="Sample gallery" widths="200px" heights="300px" perrow="2">
+Image:Test pSB1C3 ZEGFR-1907 middlelinker EGFP His.jpg
+Image:Test 30 Freiburg10 mCherry.jpg
+</gallery>
+<br/>
+====<p style="font-size:15px; background-color:#66bbff;">Test digestion of pSB1C3_001_CMV_affibody_HSPG_KO and  pSB1C3_001_CMV_VP123_587_KO_Z34C</p>====
+'''Investigator: Anna <br>'''
+<p style="font-size:13px; color:red;">Comment: 587_KO_Z34C and 587_KO_Z34C_Spacer were cloned into pSB1C3_001_CMV_VP123 as already done with the other 453 and 587 constructs (see test digestion from labday 28.09.) The test digestion looks well, nevertheless one sample out of these constructs should be sent for sequencing.  </p>
+<br/>
+{| border="1"
+| components   || align="right" |volume of pSB1C3_001_CMV_affibody_HSPG_KO /µl || align="right" |volume of pSB1C3_001_CMV_VP123_587_KO_Z34C /µl || align="right" |volume of pSB1C3_001_CMV_VP123_587_KO_Z34C_Spacer /µl
+|-
+| DNA  ||  align="right" | 3 ||  align="right" | 3 ||  align="right" | 3
+|-
+| BSA (10x) ||  align="right" | 1,5 ||  align="right" | 1,5 ||  align="right" | 1,5
+|-
+| Buffer 4 (10x)||  align="right" | 1,5 ||  align="right" | 1,5 ||  align="right" | 1,5
+|-
+|EnzymeI ||  align="right" |SspI 0,3 ||  align="right" |SalI 0,3 ||  align="right" |SalI 0,3
+|-
+|EnzymeII ||  align="right" |EcoRI 0,3  ||  align="right" |PvuII 0,3 ||  align="right" |PvuII 0,3
+|-
+|H<sub>2</sub>O||  align="right" | 4,8 ||  align="right" | 4,8 ||  align="right" | 4,8
+|-
+|'''Total volume'''||  align="right" | 15 ||  align="right" | 15 ||  align="right" | 15
+|}
+<br/>
+{| border="1"
+| Sample   || align="right" |1 || align="right" |2|| align="right" |3|| align="right" |4|| align="right" |5|| align="right" |6|| align="right" |7
+|-
+| Construct  ||  align="right" | 587_KO_Z34C ||  align="right" | 587_KO_Z34C ||  align="right" | 587_KO_Z34C||  align="right" | 587_KO_Z34C_Spacer||  align="right" | 587_KO_Z34C_Spacer||  align="right" | 587_KO_Z34C_Spacer||  align="right" | p580
+|-
+| Clone  ||  align="right" | 1 ||  align="right" | 2 ||  align="right" | 3||  align="right" | 1||  align="right" | 2||  align="right" | 3||  align="right" |
+|}
+<br/>
+{| border="1"
+| Sample   || align="right" |8|| align="right" |9|| align="right" |10|| align="right" |11|| align="right" |12
+|-
+| Construct ||  align="right" | p613||  align="right" | CMV_EGFR:1907||  align="right" | CMV_EGFR:1907||  align="right" | CMV_EGFR:1907||  align="right" | CMV_EGFR:1907
+|-
+| Clone  ||  align="right" |  ||  align="right" | 1 ||  align="right" | 2||  align="right" | 3||  align="right" | 4
+|}
+<br/>
+[[Image:Freiburg10_Test digestion of products from 29_09_10.jpg|400px|]]<br/>
+<br/>
+<br/>
+====<p style="font-size:15px; background-color:#66bbff;">Midiprep of pSB1C3_001_CMV_VP1/2/3_capins_587bla and pSB1C3_001_RC_IRCK_P5tataless clone1</p>====
+'''Investigators: Chris W. <br>
+<p style="font-size:13px; color:#003399;"> Midi-Preps of:<br/>
+pSB1C3_001_CMV_VP1/2/3_capins_587bla =P667 <br/>
+pSB1C3_001_RC_IRCK_P5tataless clone1 =P668</p> <br/>
+<br/>
+The Midi-Preps were performed according to the standard protocol yielding the following concentrations:
+{| border="1"
+| plasmid-no. || align="right" |P667|| align="right" |P668
+|-
+| concentration (ng/µl)|| align="right" |1502,3 || align="right" |991,6
+|-
+|}
+<br>
+====<p style="font-size:15px; background-color:#66bbff;"><b>Cloning of VP2/3_BAP_HSPG-KO and VP2/3_His_HSPG-KO into pCerulean_Zegfr:1907_Middlelinker and VP2/3_His_HSPG-KO into pCerulean_VP1up_NLS_mVenus</b></p>====
+<b>Investigator: Stefan </b><br>
+<p style="font-size:13px; color:red;"></p>
+Vector name:
+<ul>
+<li>pCerulean_Zegfr:1907_Middlelinker (P408)</li>
+<li>pCerulean_VP1up_NLS_mVenus (P426)</li>
+</ul>
+Insert name:
+<ul>
+<li>pBS1C3_001_VP2/3_587_BAP_HSPG-KO clone1 (P660)</li>
+<li>pBS1C3_001_VP2/3_587_BAP_HSPG-KO clone2 (P661)</li>
+<li>pBS1C3_001_VP2/3_587_His_HSPG-KO clone1 (P662)</li>
+<li>pBS1C3_001_VP2/3_587_His_HSPG-KO clone2 (P663)</li>
+</ul>
+<br />
+{| border="1"
+| '''components'''   || align="right" |'''volume for inserts (P660 - P663)  /µl'''|| align="right" |'''volume of P408  /µl''' || align="right" |'''volume of P426 /µl'''
+|-
+| DNA  ||  align="right" |10 ||  align="right" |3||  align="right" |3
+|-
+| BSA (10x) ||  align="right" |3 ||  align="right" |2||  align="right" | 2
+|-
+| Buffer 4 (10x)||  align="right" |3 ||  align="right" |2 ||  align="right" | 2
+|-
+|Enzyme NgoMIV||  align="right" |1||  align="right" |- ||  align="right" |-
+|-
+|Enzyme PstI||  align="right" |1||  align="right" |1 ||  align="right" |1
+|-
+|Enzyme MscI||  align="right" |1||  align="right" |- ||  align="right" |-
+|-
+|Enzyme AgeI||  align="right" |-||  align="right" |1 ||  align="right" |1
+|-
+|H2O||  align="right" |11||  align="right" |11||  align="right" |11
+|-
+|'''Total volume (e.g. 15,20,25,30 µl)'''||  align="right" | 30||  align="right" | 20||  align="right" |20
+|}
+<br />
+<b>Gel:</b><br />
+,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 115 Volt<br />
+<br/>
+[[Image:Freiburg10 digestion cloning BAP His to Affi Middle.jpg|450px|]]<br/>
+<br/>
+<b>Gel extraction</b>: <br>
+Was performed according to protocol.
+<br>
+<b>T4 Ligation</b>: <br>
+{| border="1"
+|ligation name || align="right" |408 + 660|| align="right" |408 + 661|| align="right" |408 + 662|| align="right" |408 + 663|| align="right" |426 + 662|| align="right" |426 + 663
+|-
+|volume of vector || align="right" |3,4 || align="right" | 3,05|| align="right" | 3,35|| align="right" | 2,56|| align="right" | 2,74|| align="right" | 3,13
+|-
+|volume of insert|| align="right" |4,6 || align="right" |4,95|| align="right" |4,65|| align="right" |5,44|| align="right" |5,26|| align="right" |4,87
+|-
+|}
+<br>
+<b>Transformation</b>: <br>
+Was performed according to standard protocol using BL21 cells.
+<br/>
+<center>[https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/October '''=> Go to Labjournal October part 1 (labday 136 - 145 )''']</center><br>
 <html>
+</div>
 </html>
-Three clones were picked (10 ml DYT, 10 µl Cm).

Team:Freiburg Bioware/NoteBook/Labjournal/September2

From 2010.igem.org

Latest revision as of 21:35, 27 October 2010

Contents

September

124. labday 19.09.2010

Continuation with Colony-PCR of pSB1C3_CD and ViralBrick motif Z34C

Testtransduction of the final modified capsid coding constructs

Miniprep of serveral constructs

125. labday 20.09.2010

Picking the clones and preparing the over-night culture

Minipreps and Sequencing of ViralBrick clones

Cloning of pCerulean_Affibody_VP2/3 and pSB1C3_Affibody_middlelinker_GFP_his

Cloning of P5_TATAless downstream of pSB1C3_001_RC_insrepcap_KpnI_back and P5 upstream of pSB1C3_001_RC_insrepcap_KpnI_back

Test digestion of VP2-N-terminal fusion constructs

BioBrick production: PCR of pAAV_RC_InsRepCap_KpnIback_VP1-ko and VP2-ko

2x repetition of CD biobrick

126. labday 21.09.2010

Trafo evalutation of CD biobrick plate

Continuation of cloning of pCerulean_Affibody_VP2/3 and pSB1C3_Affibody_middlelinker_GFP_his

Sequencing result of pSB1C3_EGFP_His upper and (!) lower band

Midi-Prep of pHelper & pSB1C3_leftITR_CMV_beta-globin_mVenus_hGH_rightITR

New aliquots (60µl) of XL1blue can be used ! (Jessica)

127. labday 22.09.2010

Sequencing results of ViralBrick ligations using dephosphorylated vector

Cloning pSB1C3_Viral Brick 587KO-empty (B274/P542) into pSB1C3_VP2/3_Capins (B438/P514)

Cellculture: Serum-free cells

PCR of P40

Mini-Prep of pSB1C3_001_RC_InsRepCap_KpnIback_VP1-ko

Cloning of CMV promotor into pSB1C3_VP123_inscap

Sequencing of Zegfr:1907-Linker Library, His-Tag and imaging appoaches

Mass Midi-Prep

RNA isolation and cDNA synthesis

cDNA synthesis

128. labday 23.09.2010

PCR of VB constructs to remove mutations

Colony PCR of new clones from the last ligations

Contuniation: Cloning pSB1C3_Viral Brick 587KO-empty (B274/P542) into pSB1C3_VP2/3_Capins (B438/P514)

Mini-Prep and test digestion of pCerulean_Affibody_VP2/3, pSB1C3_Affibody_middlelinker_EGFP_His, pSB1C3_001_RC_InsRepCap_KpnIback_VP2-ko

PCR for 587 Z34C ViralBricks

PCR of Vp1_ex, Vp2_ex and Vp3_ex and cloning into pSB1C3_001

RNA Purity Gel

hTERT PCR Reaction

Cloning of pBAD_Affibody_middlelinker_EGFP_His

Picking clones of pSB1C3_CMV_VP123_inscap

Cloning of ***** into pSB1C3_CFP

Repetition: Cloning of P5_TATAless downstream of pSB1C3_001_RC_insrepcap_KpnI_back and P5 upstream of pSB1C3_001_RC_insrepcap_KpnI_back

129. labday 24.09.2010

Sequencing results of VB 13.4

Contuniation: Cloning pSB1C3_Viral Brick 587KO-empty (B274/P542) into pSB1C3_001_VP2/3_Capins (B438/P514)

Sequencing evaluation of VP2/3_Gsat-linker and VP2/3_cap_Gsat-linker

New CD primer ordered

Sequencing of pCerulean_Zegfr:1907_VP2/3

Repetition: PCR for biobrick production: Cloning RepCap into pSB1C3

Picking clones of pSB1C3_CFP_email

MiniPreps and Test digestion of pSB1C3_CMV_VP123_capins

MiniPreps of 587 Z34C ViralBricks and pSB1C3_p40

Re-Trafo of DARPin

130. labday 25.09.2010

Sequencing of VB: 13.1, 13.4 (approach w. dephosphorylated vector, second clone picking round

Miniprep of serveral constructs

Sequencing results of pSb1C3_Affibody_middlelinker_EGFP_His

Sequencing result of pSB1C3_CMV_VP123_capins_clone1

Cloning of 453 and 587 ViralBricks into pSB1C3_CMV_VP123_capins

Sequencing results: pSB1C3_001_VP2/3_HSPG-KO

Cloning of pBAD_Affibody_middlelinker_EGFP_His and pSB1C3_Affibody_middlelinker_EGFP_His

131. labday 26.09.2010

Continuation of cloning of pBAD_Affibody_middlelinker_EGFP_His and pSB1C3_Affibody_middlelinker_EGFP_His

Picking clones of different constructs

Continuation of cloning of 453 and 587 inserts into pSB1C3_CMV_VP123_capins

Colony PCR of remaining 587 constructs

Sequencing results: pCerulean_Zegfr:1907_VP2/3

N-terminal VP2-Fusion & VP1 Insertion: Fusion of VP2/3_HSPG-KO

132. labday 27.09.2010

Sent for sequencing

Picking clones of VP1 insertion and VP2 fusion HSPG-KO approaches

MiniPreps of different constructs

Miniprep of serveral constructs

Re-Trafo of pSB1C3_pTAV (P5)

Repetition: Cloning of P5_TATAless downstream of pSB1C3_001_RC_insrepcap_KpnI_back and P5 upstream of pSB1C3_001_RC_insrepcap_KpnI_back

Cloning of * into pSB1C3_CFP

Test digestion of pCerulean_Z_EGFR:1907_MiddleLinker_VP2/3_HSPG-KO clone 2