Team:TorontoMaRSDiscovery/Notebook/April

From 2009.igem.org

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!align="center"|[[Team:TorontoMaRSDiscovery/Team|The Team]]
!align="center"|[[Team:TorontoMaRSDiscovery/Team|The Team]]
!align="center"|[[Team:TorontoMaRSDiscovery/Project|The Project]]
!align="center"|[[Team:TorontoMaRSDiscovery/Project|The Project]]
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!align="center"|[[Team:TorontoMaRSDiscovery/Parts|Parts Submitted to the Registry]]
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!align="center"|[[Team:TorontoMaRSDiscovery/Parts|BioBricks]]
!align="center"|[[Team:TorontoMaRSDiscovery/Modeling|Modeling]]
!align="center"|[[Team:TorontoMaRSDiscovery/Modeling|Modeling]]
!align="center"|[[Team:TorontoMaRSDiscovery/Bioinformatics|Bioinformatics]]
!align="center"|[[Team:TorontoMaRSDiscovery/Bioinformatics|Bioinformatics]]
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!align="center"|[[Team:TorontoMaRSDiscovery/Safety|Safety]]
!align="center"|[[Team:TorontoMaRSDiscovery/Notebook|Notebook]]
!align="center"|[[Team:TorontoMaRSDiscovery/Notebook|Notebook]]
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Revision as of 16:43, 20 October 2009



April 27, 2009

  1. Received from Rosa (SPiT):
    • TM0785
      • Plasmid containing encapsulin
      • Recommend transfect into bacteria and re-sequence
      • See email note regarding sequence error
    • 0.5 microliters TMG DNA 100 microgram/microliter
      • Use 0.4 microliter for 50 microliter PCR reaction =August 1, 2009=
  2. Overnight encapsulin cultures 1 and 6 (randomly selected) and the negative control were miniprepped
  3. The rest of the encapsulin cultures were stocked with 20% glycerol
  4. 6 digestions were done: Enc1, Enc6, Enc -ve, BB5, BB7, and C
    • 16ul of BB5 plasmid was used
    • 500ng of plasmid were used for the others
  5. The digestions were run on a 1.3% agarose gel in TAE (from here on, unless otherwise specified, all gels were 1.3% agarose)
    • BB5 was confirmed and all other parts were correct as well
  6. Overnight ligation of 7+Enc in the PCR machine