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· · · Protein Pictures 16 photos 9 comments |
· · · Protein Pictures 16 photos 9 comments |
· · · Protein Pictures 16 photos 9 comments | |||
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| Hello everyone, I need some help as I do SDS-PAGE with whole cell lysates in order to visualize my protein, however it forms monomers within the cytoplasm but upon ligand binding, it dimerizes and is translocates into the nucleus. If I treat my cells with SDS loading buffer, will it be enough to lyse both the cell membrane and the nucleus membrane, to allow proteins from both the nucleus and cytoplasm to be assayed? Would it be a better idea to extract the nucleus from the cytoplasm fraction and analyze the fractions then separately on an SDS-PAGE gel? cheers |
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