RNA electrophoresis

From OpenWetWare
Revision as of 13:18, 5 December 2006 by Reshma P. Shetty (talk | contribs)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)


Anyone should feel free to add themselves as a curator for this consensus protocol. You do not need to be a curator in order to contribute.


Electrophoresis permits assessment of RNA by size and amount. In general, electrophoresis of RNA is done as a step prior to Northern analysis.


List everything necessary to perform the protocol here. Include all information about suppliers, ordering details, etc. Links to the suppliers' page on that material are also appropriate and encouraged. Please be aware that users of this protocol may not be working in the same country as you.


Biological resources e.g. cell lines, buffers (link to a method for making them), enzymes, chemicals, kits, etc.


Any equipment used to perform the protocol (link to a method for using them).


A step by step guide to the experimental procedure.

Critical steps

  • RNA secondary structure can strongly impact how RNA electrophoreses through the gel. Therefore, electrophoresis of RNA is usually done under denaturing conditions.
  • The choice of gel matrix depends on the size range of RNAs to be analyzed. Use 3-20% polyacrylamide for RNAs < 500bp. For RNAs between 0.5-8.0 kb, use 1.5% denaturing agarose gel. For a larger size range (typically necessary for Northern analysis), use 1.0-1.2% denaturing agarose gel.


  • RNAses are the biggest problem in RNA work. Use proper precautions.


  • For best resolution, pour gels as thin as possible and run at low voltage. [1]
  • Tom Knight strongly recommends using glyoxal denaturation rather than formaldehyde denaturation due to the safety issues of formaldehyde.



  1. ISBN:0-12-249695-7 [RNAmethodologies]
  2. [MolecularCloning]
  3. Northern Hybridization of RNA Denatured by Glyoxal/DMSO Treatment doi=10.1002/0471142727.mb0409s67


Specific Protocols

  1. Knight:RNA electrophoresis