From 2007.igem.org

We must characterise the different part we are using. Essentially :

• The promoters:

1. -DAPap: we must study the basic pops when no DAP is present, and establish the pops output curve depending of

repression. look the arabinose AraC

1. -the high constitutive promoter that we are using:BBa_J23112

• cre efficience :

BBa_J5528 :Arabinose -> pBad = GFP : use it to test pbad efficiency,or make a similar construct

assemble Arabinose and cre one one plasmide, loxP ccdb loxP on another, and test the recombination frequency

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