Team:University of Ottawa/14 July 2008

From 2008.igem.org

Contents

Today in the Lab

Matt

PCR Amplification
  • Corey decided it would be best to start from the beginning and amplify the PTP2 out of Genomic DNA again. I redid the PCR and I am running it overnight.
  • Inoculation
  • 97 plasmid was inoculated from master plate so that it can glycerol stocked for tomorrow.
  • PCR Confirmation
  • Corey wanted me to do another PCR confirmation of the 97 plasmid with primers F58,F59. Expecting a band size of 2200 for this PCR when I run it on a gel for tommorrow.
  • Chris

    Digestion of AtCRE (again)
  • AtCRE was digested with EcoRI again for one hour at 37 C
  • the result was run on a 1% gel, resulting in five bands where only two were expected.
  • using Vector NTI, we figured out that the incorrect enzyme was used for the digestion; in fact, EagI should have been used instead.