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Standard protocol for Western blots with horseradish peroxidase staining

We use this protocol for the routine testing of our antibodies. It has turned out to be very robust and suitable for almost all our antibodies.

Solutions needed:

  • Blot buffer: 192 mM glycine; 25 mM Tris-base; 20 % (v/v) methanol; 0.04 % SDS.

  • Ponceau S staining solution: 5 % acetic acid, 0.1 % Ponceau S.

  • Blocking solution: 20 mM Tris-HCl, pH 7.5; 150 mM NaCl; 5 % (w/v) skimmed milk powder; 5 % normal serum (normal serum from the host-species of the secondary antibodies is recommended for blocking); 0.1 % Tween 20 without sodium azide.

  • Incubation solution: 20 mM Tris-HCl, pH 7.5; 150 mM NaCl; 0.1 % Tween 20; 5 % (w/v) skimmed milk powder.

  • Washing solution A: 20 mM Tris-HCl, pH 7.5; 150 mM NaCl; 0.1 % Tween 20

  • Washing solution B: 20 mM Tris-HCl, pH 7.5; 150 mM NaCl;

  • Staining solution: Western Lightning® Plus- ECL PerkinElmer, Inc. or comparable product.

Procedure:

The protein sample to be examined is separated by SDS PAGE and transferred to a nitrocellulose membrane by semi-dry electro-blotting using ~0.8 mA/cm2 (~0.3 mA/inch2).

  1. Stain the membrane with Ponceau S staining solution for several minutes at room temperature to check transfer.

  2. Rinse the membrane in water and incubate in blocking solution for 30 min on a lab shaker (gently rocking).

  3. Replace with fresh blocking solution containing the primary antibody in the appropriate dilution and incubate for at least 2 h on a lab shaker.

  4. Wash 3 - 4 times with incubation solution for 10 min each time.

  5. Replace with fresh incubation solution containing the recommended secondary antibody (anti-mouse IgG, anti-rabbit IgG, resp.) in the appropriate dilution and incubate for at least 1 h on a lab shaker.

  6. Wash 3 times with incubation solution for 10 min each time.

  7. Replace incubation solution with washing solution A and wash twice for 10 min each time.

  8. Replace washing solution A with washing solution B and let equilibrate for 5 min.

  9. Replace with fresh staining solution and develop (X-ray film or ECL-reader). Exposure time can be shortened or extended, if signals are extremely strong or weak, resp.




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Synaptic Systems GmbH | Rudolf-Wissell-Str. 28 | 37079 Göttingen | Germany
Phone: +49 (0)551/505 56-0 | Internet: http://www.sysy.com | E-Mail: sales@sysy.com