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Team:EPF-Lausanne/Our Project/Plasmids strategy
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(Created page with "{{:Team:EPF-Lausanne/Templates/Header|title=Plasmids strategy}} We are using TetR and LacI to inverse the repression, which allows positive selection. We will select at two lev...")
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(Created page with "{{:Team:EPF-Lausanne/Templates/Header|title=Plasmids strategy}} We are using TetR and LacI to inverse the repression, which allows positive selection. We will select at two lev...")
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Revision as of 15:24, 12 July 2011
Plasmids strategy
We are using TetR and LacI to inverse the repression, which allows positive selection. We will select at two levels: in vivo and in vitro, using either lysis cassette or RFP respectively:
- in vitro: We can test the binding of TetR directly on plates by measuring RFP fluorescence
- in vivo: The cells will grow on chemostat chips. If TetR binds to the recogintion sequence, the cells will lyse and we will be able to recover the DNA
We have one plasmid with the TetR gene, where we will introduce mutations and two plasmids for in vivo or in vitro selection:
