Team:Freiburg Bioware/NoteBook/Labjournal/August

• Perfomed with 15 µL of total volume with all four clones

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

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

Sequencing:

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

cell culture

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

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

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

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

Transduction plan

Repetition of cloning of SDM SspI and SDM PvuII

Investigator: Jessica

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

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

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

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

Test transformation of XL1 competent cells

Investigator: Kira

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

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

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

Sequencing results of ITRs

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

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

Cloning of Rep68, Rep78 and AAP into pSB1C3

Investigator: Anna

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

• Digestion of PCR products and vector:

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

• Purification of Rep68, 78 and AAP:

For the purification 95 µl of buffer PBI was used.

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

• Gelextraction of pSB1C3_RFC25_CFP:

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

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

• Quickligation of PCR products and vector:

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

• Transformation:

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

80.Labortag 05.08.2010

New LB Agar was prepared.

Investigator: Patrick

Sequenc analysis of BioBricks: CMV, hGH and beta globin

Investigator: Bea

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

Sequencing results of pSB1C3_CMV:

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

<img src="http://www.molbiotech.uni-freiburg.de/iGEM/wiki2010/images/7/74/Freiburg10_Sequence_analysis_of_PSB1C3_CMV.jpg" />

Sequencing results of pSB1C3_betaglobin:

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

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

Sequencing results of pSB1C3_hGH:

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

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

Cellculture

Investigator: Adrian


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


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

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

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

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

PCR and ligation for biobrick-production of pSB1C3_hTERT

Investigator: Anissa,Kerstin

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

• PCR:

(was performed following the standard protocol)

PCR program:

BioBrick production of pSB1C3_hTERT

Preparative gel

analytic gel

Gel extraction

Gel measurement:

• Digestion of PCR product and vector:

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

Transformation evaluation of XL1B cells and repetition of transformation

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

Cloning of SDM SspI and SDM PvuII

Investigator: Chris W.

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

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

Comment: u r right, changed (Chris)

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

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

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

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

The Ligation was performed as following:

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

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

Incubate for 30min

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

Miniprep of p158 and p159

Investigator: Bea & Volker

Plasmid Mini-Prep

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

Glycerol Stocks

TO do: Test digestion and sequencing!!!

81.Labortag 06.08.2010

Cloning Rep40 & Rep52 into pSB1C3

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

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

PCR programm of Rep40:

• 98°C 1 min

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

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

• 72°C 5 min
• Hold 4°C

PCR programm of Rep52:

• 98°C 1 min

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

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

• 72°C 5 min
• Hold 4°C

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

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

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

BioBrick Assembly of pSB1C3_beta globin_mVenus

Investigator: Bea

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

• First the plasmids P133 and P60 were digested:

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

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

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

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

For ligation the T4-Ligase were used.

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

Additionally a control ligation was performed.

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

After ligation a transformation was performed.

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

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

Test digestion of SalI SDM

Investigator: Hanna

Test digestion

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

Incubation: 1 h

Agarose-Gel:

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

• Marker: GeneRuler ladder mix

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

ITR test digestion of pAAV_MCS

Investigator: Hanna

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

Test digestion

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

Incubation: 1 h

Agarose-Gel:

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

• Marker: GeneRuler ladder mix

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

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

Miniprep of pSBC13_Rep78, pSB1C3_Rep68, pSB1C3_AAP, pSB1C3_rightITR and psB1C3_leftITR

Investigator: Kerstin

Plasmid Mini-Prep

Glycerol Stocks
pSB1C3_Rep78

pSB1C3_2_Rep78

pSB1C3_Rep68

pSB1C3_2_Rep68

pSB1C3_AAP

pSB1C3_2_AAP

pSB1C3_rightITR

pSB1C3_leftITR

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

Expected sizes:

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

• left ITR: 150bp
• right ITR: 150bp

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

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

Sequencing

P160, P165 and P170 were send for sequencing.

82.Labortag 07.08.2010

Cellculture

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

Continuation: Cloning Rep40 & Rep52 into pSB1C3

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

Mini-Prep and test digestion of pSB1C3_SDM_SspI/PvuII

Investigator: Jessica

Plasmid Mini-Prep

• new vector name: pSB1C3_SDM_SspI/PvuII

Glycerol Stocks
pSB1C3_SDM_SspI/PvuII

Test digestion

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

• Incubation: 45 min

Agarose-Gel:

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

• Marker: GeneRuler ladder mix

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

Comment:

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

Evaluation of test transformation with XL1 blue cells and pUCI

Investigator: Kira

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

Biobrick production of p5 promoter from pTAV2 and pAAV_RC

Investigator: Kira

• PCR:

DNA samples were diluted 1:100

PCR program:

Digestion of plasmid backbone:

c (pSB1C3) = 151, 1 ng/ µl

incubation @ 37 C for approx. 2 h

1% agarose gel with PCR products:

Concentrations after gel extraction:

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

Digestion of PCR products:

Concentrations after PCR purification:

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

Ligation:

Quickligase was used for ligation.

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

Transformation:

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

Sequencing results of SalI SDM

Investigator: Hanna

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

P58 can be used for further RepCap-experiments.

83. Labortag 08.08.2010

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

A431 cells were washed and received new medium.

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

84. Labortag 09.08.2010

Midi-Prep Inoculation

Investigators: Chris W., Patrick

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

Continuation: Cloning Rep40 & Rep52 into pSB1C3

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

Repetition: BioBrick production of Rep40 & Rep52

Investigator: Anna

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

PCR

PCR programm

Agarose gel

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

• Marker: GeneRuler ladder mix

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

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

Sequence analysis of pSB1C3_mGMK

Investigator: Bea

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

Results sequencing: Sequence read ok!
Primer used: VR-2
Comment: A mutation has been found in the pSB1C3 backone which was found generally in the backbone which we received from the iGEM HQ.

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

Investigator: Jessica

Bold text Mini-Prep following the standart Protokoll

• Perfomed with 10 µL of total volume with all 9 clones

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

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

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

Primer: Reverse Primer VR2

Cell culture

Investigators: Adrian, Kerstin, Patrick

Transfection on HEK293

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

Transduction of HT1080

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

Plate II

Plate III

Passaging and seeding of A431

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

BioBrick Assembly of pSB1C3_leftITR_CMV and pSB1C3_hGH_rightITR

Investigator: Bea, Achim, Jo

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

BioBrick assembly of pSB1C3_hGH_rightITR and pSB1C3_leftITR_CMV

Cloning strategy of pSB1C3_leftITR CMV

pSB1C3_hGH_rightITR

Digestion:

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

Expected sizes of constructs:

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

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

concentrations measured via NanoDrop:

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

Ligation:
For ligation, T4 ligase was used.

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

Ligation was carried out as following:

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

Incubation for 40 minutes.

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

Repetition: Cloning of SDM SspI and SDM PvuII

Investigator: Stefan

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

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

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

Digestion:

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

Expected sizes of constructs:

• pSB1C3_SDM_SspI: 1819 bp
• pSB1C3_SDM_PvuII: 981 bp

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

concentrations measured via NanoDrop:

• Sspl: 19,85 ng/µl
• PvuII: 10,57 ng/µl

Ligation:
For ligation, T4 ligase was used.

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

The Ligation was performed as following:

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

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

Incubating for 45 minutes.

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

Design and ordering of primer for P40 Promoter BioBrick production

Investigator: Hanna

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

85. Labortag 10.08.2010

Retrafo with RepCap gene (Mr.Gene)

Investigator: Bea

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

Re-transformation:

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

Continuation: Cloning Rep40 & Rep52 into pSB1C3

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

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

Investigators: Patrick, Chris W.

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

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

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

Investigator: Jessica

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

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

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

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

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

Repetition: BioBrick production of Rep40 and Rep 52

Investigator: Anna

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

PCR

PCR programm

Agarose gel

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

• Marker: GeneRuler ladder mix

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

Gelextraction

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

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

Preparation of competent XL1blue and testtrafo

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

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

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

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

Investigator: Adrian, Stefan

Plasmid Mini-Prep

• vector name: pSB1C3_SDM_SspI/PvuII

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

Test digestion

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

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

• Incubation: 45 min

Agarose-Gel:

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

• Marker: GeneRuler ladder mix

One cut is expected (PvuII in CFP).

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

Picking clones of pSB1C3_SDM_SspI/PvuII

Investigator: Stefan

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

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

86. labday 11.08.2010

Transduction of HT1080 with no AAV, AAV without GOI and AAV with 10µg

The motivation: In the past, the percentage of living cells in FACS was very low (~ 70%) so we want to check if the AAV-induced stress is responsible for cellular death, or the detaching procedure (trypsin and mechanical stress).
The plan
Plate I

Plate II

Plate III

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

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

NanoDrop concentrations:

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

Biobrick Assembly: bSB1C3_lITR_CMV & pSB1C3_betaglobin_mVenus

Investigator: Chris L., Achim

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

Digestion:

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

Expected sizes of constructs:

• pSB1C3_leftITR_CMV: 2800 bp
• pSB1C3_betaglobin_mVenus: 1200 bp, 2000 bp

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

concentrations measured via NanoDrop:

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

Continuation of Cloning of Rep40/52

Investigator: Anna

• Digestion of PCR products and vector:

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

• Purification of Rep40 and Rep52:

For the purification 95 µl of buffer PBI was used.

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

• Gelextraction of pSB1C3_RFC25_CFP:

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

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

• Ligation of PCR products and vector:

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

• Transformation:

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

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

Investigator: Anissa,Kerstin

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

• PCR:

(was performed following the standard protocol)

• PCR program:

• Digestion PCR product:

• DNA-Concentration: 4,2 ng/µl

• Purification of PCR product: (QlAquick Gel Extraction Kit)

preparation of purification was made according to the standardprotocol

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

Test digestion pSB1C3_CFP_SDM SspI and PvuII

Investigator: Stefan

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

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

• Incubation: 75 minutes
  

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

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

pSB1C3_SDM_Ssp1 (P125) sent for sequenzing

Investigator: Stefan

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

Primer used: GATC_std_pTeSp-2

Picking clones of pSB1C3_SDM_SspI/PvuII (P185)

Investigator: Adrian

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

87. labday 12.08.2010

Virus production, seeding A431 cell

Investigator: Adrian

In first place we want to create new stock of AAV without GOI, the next viral stock is with correct TK/GMK, the last stocks are with different YFP-amounts to check if the amount of GOI is a critical step for transduction effency (transgene expression).
Ten viral stocks with 3 ml each were prepared.

XL1blue are ready to use

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

Mini-Prep of pSB1C3_SDM_SspI/PvuII and pMA_RC_insert

Investigator: Stefan

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

Miniprep was performed according to protocol.

Samples were labeled:

• pSB1C3_SDM_SspI/PvuII = P185.1
• pMA_RC_insert = P190

Concentrations:

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

No test digestion was performed.

Biobrick Assembly: pSB1C3_lITR_CMV & pSB1C3_betaglobin_mVenus

Investigator: Chris L., Achim

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

Ligation:
For ligation, T4 ligase was used.

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

Ligation was carried out as following:

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

Incubation for 40 minutes.

• Transformation:

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

Repetition of cloning of bla14FM_viralbrick_MCS into pSB1C3_SDM_SspI

Investigator: Anissa

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

• Digestion of the PCR product bla14FM for 2 h :

• DNA-Concentration: 10,2 ng/µl

• Purification of PCR product: (QlAquick Gel Extraction Kit)

preparation of purification was made according to the standardprotocol

• Digestion of vector backbone pSB1C3_SDM_SspI for 2 h:

• 1 µg vector has been used

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

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

• Ligation of pSB1C3_SDM_SspI and bla14FM:

• Transformation: pSB1C3_SDM_SspI_bla14FM was transformed into BL21 following the stanard protocol

Quickchange of the EaglII restriction site in the PMA_RepCap vector

Investigator: Chris L., Achim

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

PCR-reaction:

PCR program:

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

Plasmid was transformed into XL10-Gold cells.

Sequencing results of Rep68, Rep78 and AAP BioBricks

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

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

Order oligos for CD-biobrick

Investigator: Jessica and Kira
ordered on aug 12th

BioBrick assembly of pSB1C3_leftITR_CMV_mVenus

Investigator: Stefan

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

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

Expected sizes of constructs:

• pSB1C3_leftITR_CMV: 2869 bp
• pGA14_mVenus: 2896 bp, 756 bp

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

concentrations measured via NanoDrop:

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

Ligation:

T4 ligation was performed according to protocol.

Volumes used:

• vector: 1,67 ng/µl
• insert: 6,33 ng/µl

Transformation:

bacterial strain used: XL1bB

antibiotic used for plate: chlorampenicol

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

Opened a BioBrick box

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

The first BioBricks which are in this box are:

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

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

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

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

88. labday 13.08.2010

Seeding HT1080 for transduction at saturday, Seeding HEK293 for transfection

Investigators: Kerstin, Adrian
We seeded cells according to standard protocols.

FACS of transduction from 11.8

The YFP expression is still quite low. This was kind of anticipated, the success in this experiment is the fact, that the amount of living cells is at a very high level! (~90%). The conclusion: Detach the cells fast! Use PBS which is not at 37°C (the PBS was 25min in the water bath), transfer the cells fast on ice after detaching!

The next steps are:

• Is it possible, that freeze/thaw circles reduce the transduction efficiency?
• Why is the YFP-expression that low? (~28-30%)

Continuation:pSB1C3_SDM_SspI_bla14FM

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

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

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

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

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

Design and ordering of oligos for VP fusion targeting approaches

Investigator: Hanna

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

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

Investigator: Chris L., Achim

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

Nanodrop

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

Test digestion 800ng DNA

Incubation time: 45 minutes, Incubation temperature: 37°


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

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

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

</p>

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

Investigator: Chris L.

• Ligation of PCR products and vector:

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

• Transformation:

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

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

Investigator: Hanna

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

<p style="font-size:15px; background-color:#66bbff;">pSB1C3_Rep52 (P202) sent for sequencing

Investigator: Chris L.

Primer used: Reverse Primer VR2

Repetition: Biobrick production of Rep 68, 78 and AAP

Investigator: Stefan

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

• Plasmids used as template:

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

• Primer used:

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

• PCR:

(was performed following the standard protocol)

PCR program:

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

Gel extraction

Gel extraction was perfomed according to protocol.

• Digestion of PCR products and vector:

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

• Purification of Rep68, 78 and AAP:

For the purification 200 µl of buffer PBI was used.

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

• Gelextraction of pSB1C3_RFC25_CFP:

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

c(pSB1C3)= 6,9 ng/µl

• T4 ligation of PCR products and vector:

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

• Transformation:

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

89. labday 14.08.2010

Seeding HEK293 for transfection at monday 16.8

Investigator: Kerstin, Adrian
We want to knoe which confluence of HEK293 cells is optimal for AAV production.

The plan
We seed different amounts of cells in 10 cm², and check the highest titer.

Transduction with mVenus loaded viral particles

Investigator: Kerstin, Adrian

the transduction was performed with following viral stocks:

Platte 1:

Platte 2:

Platte 3:

Platte 4: