SDS polyacrylamide-gel electrophoresis: Difference between revisions
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SDS-[[Polyacrylamide|polyacrylamide]]-gel [[Electrophoresis|electrophoresis]] is a technique used to seperate [[Proteins|proteins]] due to their net negative charge, [[Molecular weight|molecular weight]] and shape. This is achieved through creating a gel containing cross-links of [[Acrylamide|acrylamide]] subunits (polyacrylamide), which produces a matrix in which [[Proteins|proteins]] can migrate through when a electrical current is applied <ref>Alberts,Bruce et al., 2008 Pg 517</ref>. | |||
=== References === | |||
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Revision as of 18:43, 20 November 2010
SDS-polyacrylamide-gel electrophoresis is a technique used to seperate proteins due to their net negative charge, molecular weight and shape. This is achieved through creating a gel containing cross-links of acrylamide subunits (polyacrylamide), which produces a matrix in which proteins can migrate through when a electrical current is applied [1].
References
- ↑ Alberts,Bruce et al., 2008 Pg 517