IGEM:MIT/2006/Notebook/2006-8-2: Difference between revisions
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#run gel of PCR products/PCR cleanup and nanodrop BAT2 and THI3 | #run gel of PCR products/PCR cleanup and nanodrop BAT2 and THI3 | ||
#colony PCRs | #colony PCRs | ||
#make liquid cultures A,B,C from each potentially useful transformant plate | #make liquid cultures A,B,C from each potentially useful transformant plate and glycerol stocks for assembly on 8/3 | ||
==meeting topics== | ==meeting topics== |
Revision as of 13:26, 2 August 2006
to do
- analyze 42 sequence results using prepared contigs in VectorNTI -done. unfortunately our analysis shows that nothing seems to have inserted. Perhaps digests are not being run long enough? also, pchBA mutagenesis was unsuccessful.
- start isoamyl alcohol generating device work
- PCR BAT2 and THI3 again to get higher DNA concentrations for digesting/ligating on 8/3
- (3 pm) meeting with advisors
- run gel of PCR products/PCR cleanup and nanodrop BAT2 and THI3
- colony PCRs
- make liquid cultures A,B,C from each potentially useful transformant plate and glycerol stocks for assembly on 8/3
meeting topics
- troubleshoot pchBA primers
- troubleshoot pchBA mutagenesis
- troubleshoot digests/failed assemblies
- timeline of assembly work (best case scenario)
liquid cultures from potentially useful plates
- 7/31 plates: 4, 5, 6, 7, 8
- 4/5/6/7 = maybe ATF1mut-Term (colony PCR to check first)
- 8 = maybe ROO40-E0840
- 8/1 plates: 7, 8, 9
- 7/8/9 = maybe ATF1mut-Term (colony PCR to check first)