I am trying to conduct a western blot. My primary antibody is in a buffer with 0.09% sodium azide. Would this amount of azide be enough to inhibit HRP?
The azide concentration in your primary buffer should not interfer with your HRP tagged secondary antibody as it will be removed in the washing step.
Thank you. I'm having trouble with the blot signal and am trying to think of possible reasons.
@ Vince Murphy
could you give your opinion using sodium azide buffered primary antibody when in case of paraffin section?
would it interfere with HRP conjugated secondary Ab? How to avoid the possibility of interference? thanks in advance
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