Difference between revisions of "Haynes Lab:Notebook/Engineering PC-TFs/2013/09/21"

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(September 21, 2013)
(September 21, 2013)
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*Ran samples on agarose gel.
*Ran samples on agarose gel.
[[Image:noresults.jpg|250px|PEG MgCl<sub>2</sub>9/21/2013]]

Revision as of 17:26, 26 September 2013

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September 21, 2013

  • Although there was no pellet, ran a DNA Clean & Concentrator on samples.
    • Add 2 volumes of DNA Binder Buffer to each DNA sample (200 μL).
    • Place mixture in spin column into 2 ml collection tube.
    • Centrifuge at full speed for 30 seconds.
    • Add 20 μL of DNA Wash Buffer and centrifuge for 30 seconds. Repeat this step.
    • Place Zymo-Spin Column into a new 1.5 ml tube. Add 20 μL of water directly to column matrix and spin to elute DNA.
  • Ran samples on agarose gel.

PEG MgCl29/21/2013