UTDallas/15 September 2010

From 2010.igem.org

Revision as of 11:59, 21 September 2010 by Mitu (Talk | contribs)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
  • the transformations did not work from yesterday, so we decided to redigest the parts to make certain that they were actually cut with both enzymes.
  • We then ran some gels, both gels had the appropriate results so we gel purified and then ligated.
  • We also tested the Pu+GFP+Pr+XylR broths for fluorescence again, and the negative control is still as fluorescent as the others. We will try again later.
  • We incubated from glycerol stock most of the parts used today for miniprepping tomorrow.
Retrieved from "http://2010.igem.org/UTDallas/15_September_2010"