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Team:University of Ottawa/14 July 2008
From 2008.igem.org
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:'''PCR Confirmation''' | :'''PCR Confirmation''' | ||
::<li> 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. | ::<li> 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)''' | ||
| + | ::<li> AtCRE was digested with EcoRI again for one hour at 37 C | ||
| + | ::<li> the result was run on a 1% gel, resulting in five bands where only two were expected. | ||
| + | ::<li> using Vector NTI, we figured out that the incorrect enzyme was used for the digestion; in fact, EagI should have been used instead. | ||
Revision as of 19:52, 16 July 2008
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.
