Team:Warwick/Project5
Week 1
We brainstormed ideas of what we can do with the project, more specifically and also split into smaller groups of modellers and biologists (although we had daily meetings). We spent a lot of time coming up with and optimising DNA sequences for zinc fingers.
Read more Jun 29
Week 2
We marked plates, making 8 of streptomycin and chloramphenicol and 3 of chloramphenicol. We made the cells electrocompetent following lab protocol. The cells grew!
We were taught about cloning/ Gibson assembly and PCR. We did 4 mini-preps, electropheresis and several nanodrops.
Week 3
We grew up MG1655 (Z1) cells.
Put into 3ml LB, added 3l Strep and put in a shaking incubator.
We also made competent cells.
Week 4
We ligated full construct g-block into Psb1C3 plasmid backbone.
Diluted primers to 100mM, made set of 5mM primer tubes. Transformed ligated plasmid into top 10 cells (still some plasmid left in the top shelf of
the freezer). PCR: 5l 5mM forward primer
5l 5mM reverse primer
0.5l of gblock
25l of Q5 mastermix
14.5l of water
The ligated plasmid transformed cells did not grow overnight so were repeated. We undertook PCR for zf10, zf14 and zf2
Week 5
Both of the chemically transformed plates and electrotransformed plate grew over weekend.
LppompAzif268: colony PCR of clone 2 ok (inoculate culture to purify DNA inoculate 2
cultures, 4.5ml each. Miniprep them after making a glycerol stock).
Conducted plasmid miniprep of bacterial culture. Gel electrophoresis of redone PCR Pgsa worked, zf2 (all others need to be repeated at
a later stage).
Running gel of miniprep restriction digestion. Redoing PCR: INP, zf2, zf14 (67oC). zf10 (69oC) with DMSO (0%, 3%, 6%).
PCR purification of BCLA and PGSA (nanodrop returned negative, redoing). Redoing PCR of INP, zf2, zf10, zf14.
Redid PCR of INP, zf10 and zf14. zf14 returned positive, purified (31.8 ng/l. Redoing PCR of INP and zf10. Purified zf2, nanodropped.
Gel of zf10 and INP returned negative.
Redoing PCR with 66oC and 680C annealing temperatures.
Restriction digestion protocol: 5l cutsmart 10x
1l DNA
10 units enzyme each
make up to 50l water
For Nde1-Age1-HF, incubate at 370C for 5-15 minutes.
Diluted INP g-block and ZF10 g-block by a factor of 10.
Ran gradient PCR of INP and ZF10 (made 12 tubes of 20l).
Week 6
3/8/15
Redoing restriction digest of LPP-OMPA
Running gel from Friday (last time = 6.1 ng/l, issue with plasmid?)
Plasmid concentration only 5.9ng/l, running ligation anyway.
20l ligation reaction (full details in book).
4/8/15
Transforming ligated plasmid into mg1655 cells.
PCR purify INP.
Restriction digestion of INP and LPP-OMPA.
Diluted full construct g-block 10x.
Gradient PCR of LPP-OMPA full construct.
5/5/15
2 colonies from a grown DH5 Z1 plate were selected, 2 cultures inoculated, grown in shaking incubator.
Purify and restriction digest full construct.
INP digestion.
Streaked plate with PGSA and BCLA transformed cells.
6/8/15
ZF10 gel electrophoresis.
Cut out ZF10 (at 270 bases, according to ladder).
Gel extraction (freeze ‘n’ squeeze).
7/8/15
Streaked chlor plates with transformed RFP DH5 Z1 cells.
Re-streaked plates with BCLA and PGSA transformed cells.
Made chemically competent DH5 Z1 cells (frozen at -80oC).
vRan gel of digested plasmid, only obtained single band at 2000 base pairs (where backbone without RFP would be, lacking band at 1000 base pairs (for RFP gene)).
Ran gel of undigested plasmids, single band at 3000 base pairs.
Gel purified digested plasmid, nanodropped (2.1ng/l).
8/8/15
RFP and BCLA transformed cells grow with single colonies.
PGSA plate showed no growth.
Inoculated falcon tubes with RFP and BCLA. Also inoculated tube using old PGSA, incubating in shaking incubator.
Plated pure DH5 Z1 on a chlor and a clean plate (to establish background growth).
9/8/15
Miniprep of RFP, BCLA and PGSA transformed cells.
Chlor control plate grew no colonies, clean control plate grew a lawn.
Week 7
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Read more Aug 10
Week 8
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Read more Aug 17
Week 9
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Read more Aug 24
Week 10
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Read more Aug 31
Week 11
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Read more Sep 07
Week 12
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Read more Sep 14
Final Week
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Sep 21