Electrophoresis: Difference between revisions

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This section should discuss new developments in the field. Don't hesitate to drop in brief mentions of processes or features you don't intend to discuss in depth.  By so doing you are planting seeds of articles which will eventually be developed by others.<ref>"New Directions for Flocculation," American Flocculation Society. 2006. Retrieved July 21, 2009 from [http://www.amflocsoc.org/future_devs.html http://www.amflocsoc.org/future_devs.html]</ref>
This section should discuss new developments in the field. Don't hesitate to drop in brief mentions of processes or features you don't intend to discuss in depth.  By so doing you are planting seeds of articles which will eventually be developed by others.<ref>"New Directions for Flocculation," American Flocculation Society. 2006. Retrieved July 21, 2009 from [http://www.amflocsoc.org/future_devs.html http://www.amflocsoc.org/future_devs.html]</ref>
==Design and Operation==
Use lots of subsections here as you describe various aspects of the process .
==Applications==
This section should discuss how the process is used in practice.
==Examples==
If you have used a lot of equations in your article, this may be a good place to show an example of how they are used.  See the article on the Antoine Equation for an example.
==References==
<references/>


==Design and Operation==
==Design and Operation==

Revision as of 17:43, 29 November 2010

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Electrophoresis is a separation technique frequently used in the analysis of proteins and nucleic acids. The process known as electrophoresis, involves the migration of particles or molecules (in particular proteins, DNA, and RNA) through an electric field that separates them exclusively on the basis of their size or molecular weight. The direction the molecule moves depends on its charge while the rate of migration is affected by the size, shape, density of the gel and the strength of the applied current (5c). Electrophoresis is a very simple process and relatively quick with a high resolution. In addition electrophoresis is an extremely useful method to estimate the purity of a sample. The technique is also very sensitive to slight variations in molecular weight, size, and even shape of nucleic acids and proteins [1]. Electrophoresis can also be useful when it doesn’t affect the molecule’s structure or denature the protein Cite error: Invalid <ref> tag; invalid names, e.g. too many

Design and Operation

Use lots of subsections here as you describe various aspects of the process .

Applications

This section should discuss how the process is used in practice.

Examples

If you have used a lot of equations in your article, this may be a good place to show an example of how they are used. See the article on the Antoine Equation for an example.

References

  1. Harrison, R. G., Todd, P., Rudge S. R., Petrides, D. P. (2003). Bioseparations Science and Engineering. New York, NY: Oxford University Press.

Design and Operation

Use lots of subsections here as you describe various aspects of the process .

Applications

This section should discuss how the process is used in practice.

Examples

If you have used a lot of equations in your article, this may be a good place to show an example of how they are used. See the article on the Antoine Equation for an example.

References