IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-8-3: Difference between revisions

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Revision as of 16:27, 3 August 2006

To-do short term

  • PCR purify the second batch of digested KaiA/B.
  • Gel purify the excised BioBrick backbone (2kb fragment)
    • Ligate the above two products
  • Run the second batch of digested RFP BioBrick plasmid on a gel
    • Gel purify the insert
    • (Maybe) Gel purify the backbone
      • Add phosphatase to the backbone to make it ready for ligation
  • Prepare our mysterious 400b segment for sequencing