IGEM:Paris Bettencourt 2012/Notebook/RE group/Goals: Difference between revisions
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*Cloning: 1 promoter (pLac, pBAD, pRHA) with 1 restriction enzymes (I-SceI and FseI), 1 restriction site, a GFP for characterisation on the pSB3C5 plasmid. Don't forget RBS in front of GFP and in front of the restriction enzmes. ADD DRAWING | *Cloning: 1 promoter (pLac, pBAD, pRHA) with 1 restriction enzymes (I-SceI and FseI), 1 restriction site, a GFP for characterisation on the pSB3C5 plasmid. Don't forget RBS in front of GFP and in front of the restriction enzmes. ADD DRAWING | ||
<math>Ratio=\frac{CFU_{Cm}}{CFU_{Cm | <math>Ratio=\frac{CFU_{[Cm+Amp]}}{CFU_{[Cm]}}</math> | ||
Latest revision as of 13:01, 26 October 2012
Our goal
We want to obtain plasmids that have an inducible non leaky promoter, an endonuclease, and the recognition site for the endonuclease on the plasmid.
- We want to test a few things: that the restriction enzympe is expressed, that the restriction enzyme cuts at its restriction site, and that the promoter is not leaky.
- Cloning: 1 promoter (pLac, pBAD, pRHA) with 1 restriction enzymes (I-SceI and FseI), 1 restriction site, a GFP for characterisation on the pSB3C5 plasmid. Don't forget RBS in front of GFP and in front of the restriction enzmes. ADD DRAWING
[math]\displaystyle{ Ratio=\frac{CFU_{[Cm+Amp]}}{CFU_{[Cm]}} }[/math]
