IGEM:MIT/2006/Notebook/2006-10-6

Kate

1. Digest 250/400 double plasmids with XP -done, KB, VV
2. Repeat digest of missing 250 with ES -done, KB
3. Ligate final constructs -done, KB
4. Transform final constructs in Jason's competent cells -done, KB
5. Start an LC of plain IK cells in plain LB -done, KB

Andre

1. Locate iGEM glycerol boxes and put into Grossman Lab -done, AG
2. Make an estimate of plates needed for streaking parts -done, AG