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Team:University of Ottawa/11 June 2008
From 2008.igem.org
Contents |
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.
