Difference between revisions of "Alm:Agarose gel electrophoresis"

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*6X loading dye
*[[Agarose_gel_loading_dye|6X loading dye]]
*[[TAE]] + agarose 1%
*[[TAE]] + agarose 1%
*1X [[TAE]] (~200ml)
*1X [[TAE]] (~200ml)

Revision as of 12:53, 20 September 2007


How to use gel electrophoresis to separate, measure and visualize DNA pieces.




  1. Microwave TAE agarose 1% to melt. Pour 30 ml for a small gel into a small flask/beaker to cool a bit, then pour into the gel box with the correct comb for your size/number of samples.
  2. Add 6x loading dye to your samples.
  3. Make sure the red electrode is at the opposite end from the wells. You can check the progress of the DNA with the loading dyes to check the direc
  4. Set the time and settings on the power supply by pressing Mode to change fields. (typical settings for DNA: 90V constant voltage, 45 minutes)
  5. Slide on the lid and start the power supply.

Staining and visualization

  • Wear blue/purple nitrile gloves when handling the items at the staining station and the gel imager.
  1. Place the gel in the plastic box.
  2. Stain for 1 hour in EtBr solution (concentration??).
  3. Pour the EtBr back into the light-proof bottle.
  4. Destain with used TAE for 2 minutes.
  5. Pour the TAE back into the bottle.
  6. Image the gel on a UV light box or the computerized gel imager in the Polz lab.
  7. Print out the image for your notebook, annotating the lanes, marker, and bands.
  8. Note agreement with/variation from expected result.



  • Arne Materna
  • Sean Clarke