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Team:Mississippi State/15 August 2008
From 2008.igem.org
Revision as of 18:05, 16 October 2008 by Caleb Dulaney (Talk | contribs)
- prepare and run gel on plasmid extraction
- digest plasmid to check for gene
- there was no insert, and mistake was made in not adding IPTG and PGAL to the plates.
- Dr Ma: do pcr w/ lip using 2nd primers and taq, load all onto gel, cut out, and purify. Ligate w/ pGEM, transform into e coli, plate, extract
