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Western blot detection of membrane proteins I need to detect MRP1, a membrane protein, by western blot and have been unable to do so. Do membrane proteins require higher concentrations of detergent in order to be soluble in lysis solution? What is the ideal lysis buffer? Thanks. |
Western blot detection of membrane proteins Samuel C McNeely wrote: You need an antibody that works in Westerns (that is, against the denatured protein). Large trans-membrane proteins like ABC-transporters blot better in thank than in semi-dry blotters, and Dunns buffer (with 50 uM SDS) works better than Towbins. Like with all glycoproteins, you may consider doing an Eastern rather than a Western blot. It may also be advantageous not to use a whole cell lysate but to enrich the plasma membrane by isopycnic centrifugation (table top ultracentrifuges with 0.2 ml sample tubes are ideal) and then process that. This limits the number of proteins in the lysate, but requires a larger sample size for the additional handling. Hypotonically lyse the cells to ghosts, collect by centrifugation, then potter and crap-spin. A 1-step sucrose gradient (35%) is then used to collect the PM at the interface between sample and sucrose. |
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