Team:Paris/August 17
From 2008.igem.org
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+ | =Creation of a registry of pFliL, pFlhDC, and ''FlhDC''= | ||
=='''Analysis of the other transformation we did [[Team:Paris/August 16 |yesterday]]'''== | =='''Analysis of the other transformation we did [[Team:Paris/August 16 |yesterday]]'''== | ||
===Evaluation of the number of colonies=== | ===Evaluation of the number of colonies=== | ||
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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'''. | 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= |
===Evaluation of the number of colonies=== | ===Evaluation of the number of colonies=== | ||
Latest revision as of 18:24, 4 September 2008
Construction of pLas-TetR-GFP tripart & rbs-LasR-dble terAnalysis of the transformation we did yesterday
PCR Screening
Conclusion : Minipreps & Stocks
Creation of a registry of pFliL, pFlhDC, and FlhDCAnalysis 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
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