Why must
1. electrophoresis of the protein sample, and
2. transfer to nitrocellulose
precede the actual probing of the sample with an antibody?
Electrophoresis must occur to seperate the protein while the transfer to the membrane allows the antibodies to properly attach to the protein that you are interested in.
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What are some common treatments that could be used to disrupt the antibody-antigen complexes?
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What is the need for serial dilution of the sample when performing an Elisa?
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What is the function of the enzyme bound to the secondary antibody?
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What are the differences and similarities between western blotting and immunohistology?
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