IGEM:MIT/2006/Notebook/2006-10-7

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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
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