Protein blot (Western) hub

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(Relevant lab protocols)
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*[[Ketner: Tissue culture viral lysate Western Blot]]
*[[Ketner: Tissue culture viral lysate Western Blot]]
*[[Western Blot/Tissue Preparation|Tissue preparation for western blot]]
*[[Western Blot/Tissue Preparation|Tissue preparation for western blot]]
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[[Category:Protocol]]
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[[Category:In vitro]]
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[[Category:Protein]]

Revision as of 13:42, 9 May 2007

Overview

A Western Blot allows for the semiquantitative determination of protein expression. Crude cell lysates are loaded into a polyacrylamide gel containing a denaturing agent which give all the proteins a net negative charge. A current can then be passed through the gel and the proteins will migrate through the gel, with the largest proteins traveling the slowest, resulting in a lane where proteins become separated on the basis of their weight. The proteins can then be transferred from the gel onto a membrane (often nitrocellulose or PVDF), which can then by incubated with an antibody directed against the protein of interest. By using a detector conjugated to an antibody one can now detect specifically the protein of interest.

Relevant lab protocols

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