Electrophoresis: Difference between revisions
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As shown in the diagram, the nucleic acids or proteins are loaded into the wells or depressions at one end on the eletrophoretic medium (also known as a gel). The apparatus also has two electrodes on either side of the eletrophoretic medium. The anode is positively charged while the cathode is negatively charged. When a power source connects the two electrodes the charged particles begin to migrate towards the oppositely charged electrode due to the electric potential field within the media (1). | As shown in the diagram, the nucleic acids or proteins are loaded into the wells or depressions at one end on the eletrophoretic medium (also known as a gel). The apparatus also has two electrodes on either side of the eletrophoretic medium. The anode is positively charged while the cathode is negatively charged. When a power source connects the two electrodes the charged particles begin to migrate towards the oppositely charged electrode due to the electric potential field within the media (1). | ||
== | == Electrophoretic Mediums == | ||
== | == Detection Techniques == | ||
== | == Gel Electrophoresis of DNA and RNA == | ||
== | == Gel Electrophoresis of Proteins == | ||
== Native Electrophoresis == | |||
== | == Denaturing Gel electrophoresis == | ||
== | === Disadvantage/Advantage === | ||
== Isoelectric focusing == | |||
== | == Two-Dimensional Electrophoresis for Proteins == | ||
== Two-Dimensional Electrophoresis for DNA and RNA == | |||
== Blotting Techniques == | |||
== Advantages & Disadvantages of Electrophoresis == | |||
==References== | ==References== | ||
<references/> | <references/> |
Revision as of 22:51, 30 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>
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Generation of Heat in Electrophoresis Instrumentation
As shown in the diagram, the nucleic acids or proteins are loaded into the wells or depressions at one end on the eletrophoretic medium (also known as a gel). The apparatus also has two electrodes on either side of the eletrophoretic medium. The anode is positively charged while the cathode is negatively charged. When a power source connects the two electrodes the charged particles begin to migrate towards the oppositely charged electrode due to the electric potential field within the media (1).
Electrophoretic Mediums
Detection Techniques
Gel Electrophoresis of DNA and RNA
Gel Electrophoresis of Proteins
Native Electrophoresis
Denaturing Gel electrophoresis
Disadvantage/Advantage
Isoelectric focusing
Two-Dimensional Electrophoresis for Proteins
Two-Dimensional Electrophoresis for DNA and RNA
Blotting Techniques
Advantages & Disadvantages of Electrophoresis
References
- ↑ Harrison, R. G., Todd, P., Rudge S. R., Petrides, D. P. (2003). Bioseparations Science and Engineering. New York, NY: Oxford University Press.