Copenhagen/18 August 2011

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Thursday

Lab work

  • TLC on A1
  • Membrane preparation on A2
  • Run SDS-page on A2
  • The bonds at the SDS-page from yesterday with A1 was unforunately not where the suppose to have been. Maybe there is a problem with the promoter we use...
  • USER cloning with A2, B1, 2C9 and 1A2
  • Transformation with orginal CYPs (before the mutations) to use for a control in next week


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