Team:University of Ottawa/19 July 2008
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Djedrysiak (Talk | contribs) (New page: __TOC__ ==Today in the lab== '''Dan''' :'''Ligation''' ::<li>Spiked my overnight ligation with 1 uL ATP and 1 uL enzyme.) |
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__TOC__ | __TOC__ | ||
==Today in the lab== | ==Today in the lab== | ||
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:'''Ligation''' | :'''Ligation''' | ||
::<li>Spiked my overnight ligation with 1 uL ATP and 1 uL enzyme. | ::<li>Spiked my overnight ligation with 1 uL ATP and 1 uL enzyme. | ||
+ | :'''Ligation of Atcre''' | ||
+ | ::<li> Began ligation of Chris's Atcre component in ~50 uL reaction | ||
+ | '''Matt''' | ||
+ | :'''Inoculation''' | ||
+ | ::<li>Today I took out the inoculated bacteria from Friday and put them in the -4 fridge (PTP2). All of the bacteria grew and the control was clean. | ||
+ | ::<li>I also inoculated both BY4742 WT and YPH500 WT for Katy for a Mass Spec test. | ||
+ | :'''PCR''' | ||
+ | ::<li>I also performed a PCR cleanup of the 600/01 plasmids after I confirmed them on a Gel. These plasmids will now be ready for integration next week. |
Latest revision as of 18:30, 30 July 2008
Contents |
Today in the lab
Dan
- Ligation
- Spiked my overnight ligation with 1 uL ATP and 1 uL enzyme.
- Ligation of Atcre
- Began ligation of Chris's Atcre component in ~50 uL reaction
Matt
- Inoculation
- Today I took out the inoculated bacteria from Friday and put them in the -4 fridge (PTP2). All of the bacteria grew and the control was clean.
- I also inoculated both BY4742 WT and YPH500 WT for Katy for a Mass Spec test.
- PCR
- I also performed a PCR cleanup of the 600/01 plasmids after I confirmed them on a Gel. These plasmids will now be ready for integration next week.