Team:TorontoMaRSDiscovery/7 August 2009

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August 7, 2009

  1. Started overnight cultures of 1+2 sample 1,2,4
  2. Retransformed BB1 using the iGEM 2007 Toronto team's protocol (heat shock for 90s) and plated on Amp plates
  3. Plated DH5alpha cells as a control on plain LB plates
      • This is thumotoga maritime genomic DNA for purpose of re-cloning
  4. Microcentrifuge tubes 1 and 2 placed in -20 freezer
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