Haynes Lab:Notebook/David Barclay Undergrad Training/Plasmid Transformation/2015/07/28: Difference between revisions
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(Autocreate 2015/07/28 Entry for Haynes_Lab:Notebook/David_Barclay_Undergrad_Training/Plasmid_Transformation) |
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==Gel Electrophoresis== | |||
*1% Agrose gel | |||
**6μL sybr gel stain | |||
*Digests | |||
**DNA - 5.0μL | |||
**10x FD buffer - 1.5μL | |||
**ECO RI - 1.0μL | |||
**Pst I - 1.0μL | |||
**dH2O - 6.5μL | |||
*Sample 1: DNA from colony 1 | |||
*Sample 2: DNA from colony 2 | |||
**Incubated at 37°C for 15 min | |||
*Electrophoresis | |||
**1kbt ladder - 10μL | |||
**Sample 1 - 15μL | |||
**Sample 2 - 15μL | |||
**Gel ran for 45 min | |||
[[Image:IMG 1099.PNG|400px|Today's gel]]<br>15 μL/lane; 1% agarose; [http://openwetware.org/wiki/Image:KAH_Fermentas_GeneRuler_1kbplus.jpg Ladder] | |||
Revision as of 15:37, 28 July 2015
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Gel Electrophoresis
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