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CLAMP modulates the stability of SR-BI protein. CHO cells and CHO-CLAMP cells were transiently transfected with or without either SR-BI or SR-BIΔC15. Western blotting analysis was performed in the corresponding cellular lysates by using an anti-SR-BI antibody. Bands corresponding to SR-BI were quantified by using LAS-1000 (Fuji). Data represent samples from a typical experiment.
