Western Blots: Difference between revisions

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== SDS-PAGE Westerns ==
#redirect [[Western blot]]
=== 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.
 
=== Materials ===
*2x PLS
*PBS-T
*5% milk in PBS-T
 
===Procedure===
====Prepare Samples====
*Boil Samples for 5 min, cool on ice 1 min, spin 1 min
*Ladders: 8ul ladder + 8ul 2x PLS
**High mol weight 30KDa - 220 KDa
**Low mol weight 6.5KDa - 45 Kda

Revision as of 10:37, 6 September 2006

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