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Team:University of Ottawa/7 August 2008
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:<li> Ran products on a 0.6% gel for 1.5 hours at 80V. Stained the gel in an Ethidium Bromide and TAE Buffer solution for 20 minutes. | :<li> Ran products on a 0.6% gel for 1.5 hours at 80V. Stained the gel in an Ethidium Bromide and TAE Buffer solution for 20 minutes. | ||
:<li> Excised desired band and performed gel extraction. Stored at -20°C. | :<li> Excised desired band and performed gel extraction. Stored at -20°C. | ||
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| + | =='''Matt'''== | ||
| + | |||
| + | :<li> Absorbance was measured from the ten colonies miniprepped by Chris. I then digested each colony with PST1 to confirm. | ||
| + | :<li> All colonies were confirmed and successful. | ||
| + | :<li> I used SLN1 primers to amplify the PTP2/GAL10 casette overnight from two colonies chosen from the miniprep. | ||
Revision as of 16:34, 8 August 2008
Today in the Lab
Chris
Digestion and Ligation of OA, OB and T Amp Product
- Digested all three according to previous digestion protocol (see August 5 post). Ran 7 samples--six ligations and one digestion products only. Incubated at 37°C for 15 minutes, followed by 20 minutes at 80°C to denature.
- Spiked each tube with ligase and ATP then incubated at room temperature for around two hours.
- Ran products on a 0.6% gel for 1.5 hours at 80V. Stained the gel in an Ethidium Bromide and TAE Buffer solution for 20 minutes.
- Excised desired band and performed gel extraction. Stored at -20°C.
Matt
- Absorbance was measured from the ten colonies miniprepped by Chris. I then digested each colony with PST1 to confirm.
- All colonies were confirmed and successful.
- I used SLN1 primers to amplify the PTP2/GAL10 casette overnight from two colonies chosen from the miniprep.
