Team:Paris/August 17
From 2008.igem.org
(Difference between revisions)
(→Evaluation of the number of colonies) |
(→Evaluation of the number of colonies) |
||
Line 188: | Line 188: | ||
Remarks: <br> | Remarks: <br> | ||
L143 and L144 did not work once again. Maybe there is a problem with the digestion, <br> because the primers used present only two nucleotides after the restriction sites. what we should <br>do is cutting pfliL with xbaI and SpeI. As the vector will autoligate, we should use a phosphatase <br> to prevent this phenomenon. <br> | L143 and L144 did not work once again. Maybe there is a problem with the digestion, <br> because the primers used present only two nucleotides after the restriction sites. what we should <br>do is cutting pfliL with xbaI and SpeI. As the vector will autoligate, we should use a phosphatase <br> to prevent this phenomenon. <br> | ||
- | For L147 and its control (T4), we do not observe any red fluorescence. It means that the digestion work well, because if it was not digested, the strong promoter J23100 | + | For L147 and its control (T4), we do not observe any red fluorescence. It means that the digestion work well, <br>because if it was not digested, the strong promoter J23100 should express mRFP! <br> '''We will repeat all the ligation anyway'''. |
=='''Construction of OmpR*+RBS and EnvZ*+RBS: transformation'''== | =='''Construction of OmpR*+RBS and EnvZ*+RBS: transformation'''== |
Revision as of 18:22, 4 September 2008
Construction of pLas-TetR-GFP tripart & rbs-LasR-dble terAnalysis of the transformation we did yesterday
PCR Screening
Conclusion : Minipreps & Stocks
Analysis of the other transformation we did yesterdayEvaluation of the number of colonies
Remarks: Construction of OmpR*+RBS and EnvZ*+RBS: transformationEvaluation of the number of colonies
|