Cloning in BioBrick vectors

From 2007.igem.org

Revision as of 14:39, 15 October 2007 by Robertina (Talk | contribs)

We have amplified with PCR our promoters and Pho80 coding sequence and we have loaded 1µl on the gel to see if there were aspecific products or others. 1ORE-CYCtata

2XORE-CYCtata

FOX3promoter

PHO80cds

In the same time we have transformed plasmid pBS1A3 in competent cells and after MIDI-prep we have loaded 1µl on the gel. We have digested in two differents ways our plasmid to be sure of it's identity! Then we have digested it with XbaI and SacII and we have loaded all digest product on gel to separate by gel extraction the insert from plasmid!