SDS polyacrylamide-gel electrophoresis: Difference between revisions

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 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.
&nbsp;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&nbsp;acrylamide subunits (polyacrylamide), which produces a matrix in which proteins can migrate through when a electrical current is applied.&nbsp;<references />Alberts,Bruce et al(2008) Molecular Biology of the Cell(5th edition) Garland Science Pg 517
<ref>Alberts,Bruce et al(2008) Molecular Biology of the Cell(5th edition) Garland Science Pg 517</ref>

Revision as of 18:08, 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. Alberts,Bruce et al(2008) Molecular Biology of the Cell(5th edition) Garland Science Pg 517