Team:University of Ottawa/11 June 2008

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Today in the Lab

Dan, Matt

Gel Electrophoresis + PCR
  • Plasmids 7 + 8 were unsuccessful upon verifying with the Gel. The bands did not appear in the correct location.
  • We decided to redo these plasmids with the primers F50 + F51, perform PCR and run the Gel tommorrow morning .
  • Plasmids 0 + 1 turned out to be successful, tomorrow we will perform a DNA clean up with these plasmids. Mila is going to show us how to do this.
  • Tomorrow we also plan on performing a DNA clean up with Plasmids 7,8 if the Gel is successful.
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