Team:Paris/July 30
From 2008.igem.org
(→Results of transformations) |
|||
Line 56: | Line 56: | ||
|- | |- | ||
|align="center"|L107 | |align="center"|L107 | ||
- | |align="center"|Strongest promoter - ECFP<br>D103 (BV) - | + | |align="center"|Strongest promoter - ECFP<br>D103 (BV) - D130 (BI) |
|align="center"|Amp | |align="center"|Amp | ||
|align="center"|a lot | |align="center"|a lot | ||
Line 62: | Line 62: | ||
|- | |- | ||
|align="center"|L108 n°2 <br>(the right one) | |align="center"|L108 n°2 <br>(the right one) | ||
- | |align="center"|Strong promoter - gfp Tripart<br>D103 (BV) - | + | |align="center"|Strong promoter - gfp Tripart<br>D103 (BV) - D131 (BI) |
|align="center"|Amp | |align="center"|Amp | ||
|align="center"|+/- 100 | |align="center"|+/- 100 | ||
Line 140: | Line 140: | ||
|- | |- | ||
|align="center"|L120 | |align="center"|L120 | ||
- | |align="center"|tetR repressible - ECFP<br>D106 (BV) - D130 (BI) | + | |align="center"|tetR repressible promoter - ECFP<br>D106 (BV) - D130 (BI) |
|align="center"|Amp | |align="center"|Amp | ||
|align="center"|a lot | |align="center"|a lot | ||
Line 146: | Line 146: | ||
|- | |- | ||
|align="center"|L121 | |align="center"|L121 | ||
- | |align="center"| | + | |align="center"|tetR repressible promoter - gfp tripart<br>D106 (BV) - D131 (BI) |
|align="center"|Amp | |align="center"|Amp | ||
|align="center"|a lot | |align="center"|a lot | ||
Line 158: | Line 158: | ||
|- | |- | ||
|align="center"|L123 | |align="center"|L123 | ||
- | |align="center"|RBS lasI - | + | |align="center"|RBS lasI - gfp tripart<br>D107 (BV) - D131 (BI) |
|align="center"|Amp | |align="center"|Amp | ||
|align="center"|1 | |align="center"|1 | ||
Line 164: | Line 164: | ||
|- | |- | ||
|align="center"|L124 | |align="center"|L124 | ||
- | |align="center"|Strongest RBS - | + | |align="center"|Strongest RBS - gfp<br>D102 (BV) - D122 (BI) |
|align="center"|Amp | |align="center"|Amp | ||
|align="center"|a lot | |align="center"|a lot | ||
Line 271: | Line 271: | ||
|align="center"|ok | |align="center"|ok | ||
|} | |} | ||
- | |||
==Analysis of yesterday DNA digestion== | ==Analysis of yesterday DNA digestion== |
Revision as of 17:52, 12 August 2008
Results of transformations
Analysis of yesterday DNA digestionThe digested DNA of yesterday was analysed one more time by electrophoresis on a 0.8% agarose gel (about 30 minutes at 100 W).
==> Conclusion :Each of the samples was succesfully digested and purified except for the sample D108. It seems that the QIAprep columms (from the QIAGEN Minipreps kit) can be used instead of the QIAquick columms (for DNA Gel Extraction).
PCR Screening of Ligation TransformantsUse of 8 clones of Ligation transformants for screening PCR
Protocol of screening PCR
Conditions of electrophoresis
Results
But we don't observe results for L102(3), L102(6), L103(4), L106(1), L106(2), L106(4), L111(1) Migration of an another gel for this sample...
|