Ketner: Tissue culture viral lysate Western Blot

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(Prepare Gel)
(Procedure)
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*Fill with 1x running buffer
*Fill with 1x running buffer
*Load samples and run at 50-120V
*Load samples and run at 50-120V
 +
 +
=====Transfer to membrane====

Revision as of 13:46, 6 September 2006

Contents

SDS-PAGE Westerns

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

Prepare Gel

This will vary according to gel apparatus

  • Clean and assemble gel apparatus
  • Boil agar to create plug
  • Drip agar down side of cassette with pasteur pipette, just enough to form seal
  • Create running gel
  • Layer isopropanol on top to remove bubbles
  • When hardened create stacking gel
  • Cast stacking gel with comb, remove comb when hardened
  • Fill with 1x running buffer
  • Load samples and run at 50-120V

=Transfer to membrane

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