[Home]History of Gel electrophoresis

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Revision 5 . . December 17, 2001 5:52 am by (logged).234.79.xxx [*free linked autorad to [[isotopic tracer]]]
Revision 4 . . December 9, 2001 7:34 pm by (logged).234.79.xxx [*methods of visualization, expansion on concept of one-band-per-component, resolution of components]
Revision 3 . . September 19, 2001 4:06 pm by Magnus Manske [Some more, needs better English]
  

Difference (from prior major revision) (author diff)

Changed: 3c3,4
After the electrophoresis run, when the smallest molecules have almost reached the anode, the molecules in the gel can be stained? to make them visible. Silver or Coumassie blue dye can be used. Other methods can also be used to visualize the separation of the mixture's components on the gel. If the analyte molecules luminesce under ultraviolet light, a photograph? can be taken of the gel under ultraviolet light. If the molecules to be separated contain radioactive atoms, an autoradiogram? can be recorded of the gel.
After the electrophoresis run, when the smallest molecules have almost reached the anode, the molecules in the gel can be stained? to make them visible. Silver or Coumassie blue dye can be used. Other methods can also be used to visualize the separation of the mixture's components on the gel. If the analyte molecules luminesce under ultraviolet light, a photograph? can be taken of the gel under ultraviolet light. If the molecules to be separated contain radioactive atoms, an
autoradiogram can be recorded of the gel.

Changed: 10c11
*Gel elctrophoresis of DNA or RNA is usually done by agarose gel electrophoresis.
*Gel elctrophoresis of DNA or RNA is usually done by agarose gel electrophoresis.

Changed: 14,16c15
:Back to : genetics -- biochemistry -- molecular biology


:Back to : genetics -- biochemistry -- molecular biology

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