So in reducing sds, you add bme or another. If we had a heterotrimer, we would only see one band. A reducing agent can break disulfide bonds, and for a majority of proteins, this will not. Samples can be reduced or nonreduced.
If we had a heterotrimer, we would only see one band. So in reducing sds, you add bme or another. Samples can be reduced or nonreduced. If we had a heterotrimer, we would only see one band. A reducing agent can break disulfide bonds, and for a majority of proteins, this will not.
