Copenhagen/18 August 2011

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(Created page with "'''Thursday''' '''Lab work''' * TLC on A1 * Membrane preparation on A2 * Run SDS-page on A2 * The SDS-page from yesterday with A1 was..... * USER cloning with A2, B1, 2C9 and 1A...")
 
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* Membrane preparation on A2
* Membrane preparation on A2
* Run SDS-page on A2
* Run SDS-page on A2
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* The SDS-page from yesterday with A1 was.....
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* 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
* USER cloning with A2, B1, 2C9 and 1A2
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* Transformation with orginal CYPs (before the mutaions) to use for a control in next week
+
* Transformation with orginal CYPs (before the mutations) to use for a control in next week
 +
 
 +
 
 +
 
 +
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Latest revision as of 14:23, 18 August 2011

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


Back to Notebook