Electrophoresis

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Extraction is the technique of removing nucleic acids (DNA and/or RNA) from surrounding cellular material and is the first step before subsequent molecular analysis.

Click here to learn about extraction equipment.

Electrophoresis allows DNA, RNA and protein fragments to be separated by size as they move through a charged gel matrix. It uses a charge delivered by a power supply of approximately 100 amps to separate molecules by their charge to mass ratio. Few pieces of equipment are necessary to perform slab gel electrophoresis. All pieces of equipment are quite small, fit on the bench top, are relatively inexpensive and are made by many manufacturers. An alternative to slab gel electrophoresis which also separates proteins or small nucleic acids by size ratio is gel capillary electrophoresis. Using a gel capillary electrophoresis instrument, only minimal amounts of DNA are needed as compared to the slab gel technique. The capillary electrophoresis instrument can also use alternate separation methods, such as dye terminator sequencing.

Click here  to learn more about electrophoresis methods.

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References

  • Text – http://web.utk.edu/~khughes/GEL/sld001.htm
  • Text – http://www.abrf.org/JBT/1999/September99/sep99mardis.html
  • Text – http://www.sumanasinc.com/webcontent/animations/content/gelelectrophoresis.html
  • Images – http://joagene.com/tag/UV?TSSESSION=135b375144aac06b2ce9022079e38c73 
  • Images – http://pages.usherbrooke.ca/dgarant/DG%20eng/lab_infrastructure.htm
  • Images – http://www.ecs.umass.edu/eve/facilities/micro.html 
  • Images – http://www.sci.sdsu.edu/dnacore/sdsu_dnacore.html

 

 

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