I'm interested in determining if my protein is running as a dimer (or higher). I have a peptide antibody that works on denatured protein but when I ran a non-reducing gel, the antibody did not recognize the protein. I would like to be able to denature the protein in the (non-reducing) gel after it has run to determine if the protein is running as an oligomer. Does anyone know how I would go about denaturing the protein in the gel?
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mdfenko
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an elder
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Excellent
Excellent
Posted 20 March 2009 - 08:33 AM
you could try soaking in sds and 2-me (or dtt).
or you could try transferring then soaking in sds and 2-me to denature on the membrane.
or you could try transferring then soaking in sds and 2-me to denature on the membrane.
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