Haynes Lab:Notebook/Engineering PC-TFs/2012/10/16: Difference between revisions
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==Summary== | ==Summary== | ||
* | Gel Electrophoresis | ||
*Follow steps for gel electrophoresis. | |||
*Orient top notch of gel electrophoresis apparatus. Place gel tray into larger tray. | |||
*Create 1% gel by putting .6 grams of agarose into flask. | |||
*Microwave agarose solution for 40 seconds | |||
*Using hot gloves, grab flask out of microwave and swirl flask vigorously. Place back in microwave for 30 more seconds. | |||
*When flask is taken out of microwave, make sure that the agarose is completed dissolved. | |||
*Set up wells on gel electrophoresis apparatus. The mold for the first digest is B-10. Use the large "teeth" and slip in the notches. | |||
*Add EtBr (ethidium bromide) to the agarose gel. There should be 1 microliter of EtBr per 10ml of agarose gel. Therefore, 6 µL. | |||
*Pour gel into tray. Wait twenty minutes for gel to settle. | |||
*Wash the agarose gel flask. | |||
*Pipette 15 μL of DNA ladder into first well. Pipette 45μL of PCR reactions into subsequent wells. | |||
*Turn on electrophoresis and let run for thirty minutes. | |||
[[Image:October_16_gel.jpg|400px|thumb|left|]] | |||
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Revision as of 13:15, 21 October 2012
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SummaryGel Electrophoresis
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