The following western blot protocol was used in the validation of some Aviva products. This protocol will be linked to the product pages.

1.  Block membrane by incubating 1 hour at room temperature with shaking in Blocking Solution (5%nonfat milk in TBST (50mM Tris, 100mM NaCl, 0.05% Tween-20, pH 7.6)). Note: Use 5% BSA in Blocking Solution for phosphor specific antibodies.

Incubation with Primary Antibody
2.  Dilute primary antibody at the appropriate dilution in Blocking Solution.
3.  Incubate the membrane with diluted primary antibody overnight at 4C with agitation.
4.  Remove antibody solution. Wash the membrane 3 times for 5-10 minutes each time at room temperature in TBST (50mM Tris,100mM NaCl, 0.05% Tween-20, pH 7.6) with shaking.
Note: Increase the concentration of Tween-20 to 0.1% reduces the background and increases the specificity, but it will reduce the sensitivity.

Incubation with Second Antibody
5.  Incubate membrane with secondary AP conjugate diluted (according to manufacturer’s instructions) in Blocking Solution for 1 hour at room temperature with shaking.
6.  Repeat Step 4.
7.  Wash membrane with TBS for 2-5 minutes before proceeding Chemiluminescent Reaction.

Chemiluminescent Reaction
8.  Prepare and use the Chemiluminescent substrate according to the manufacturer’s instructions.
9.  Immediately wrap the membrane and expose to X-ray films for 10 second to 1 hour period. The exposure time may vary according to the mount of antibody and antigen.

Peptide Competition
10. Before proceeding Western Immunoblotting, add Blocking Peptide to the diluted primary antibody in a molar ratio of 10:1 (peptide to antibody) and incubate the mixture at 4C for overnight or at room temperature for 2 hours.