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GRP78 degradation is induced by different toxins in peritoneal macrophages. Peritoneal macrophages were treated with DON, tunicamycin (Tuni), roridin A (RA), satratoxin G (SG), ricin, and T-2 toxin for 3 or 6 h. GRP78 protein was measured by Western blot. RI indicates relative intensity which is the percentage of the maximal fluorescence in the same lane.
