Figure 7.
Gβ interacts with endogenous GRK2 in platelets ex vivo but Gqα does not. (Ai) GST-GRK2 was immunoprecipitated from human or mouse platelets, and samples were probed for Gqα or Giα2. Glutathione S-transferase (GST) reprobe indicated the equal loading. n = 2. (Aii) Human platelet lysate from resting or 1 U/mL thrombin-stimulated platelets in the presence or absence of GDP+AlF4– were subjected to immunoprecipitation of GRK2 and probed for Gq. n = 3. (B) GRK2 from resting and thrombin-stimulated (1 U/mL) human platelet lysate was immunoprecipitated with the specific mouse anti-GRK2 antibody and probed for Gβ. GRK2 was reprobed with an anti-GRK2 antibody. n = 6. A marker line was excised as indicated by the vertical line.

Gβ interacts with endogenous GRK2 in platelets ex vivo but G does not. (Ai) GST-GRK2 was immunoprecipitated from human or mouse platelets, and samples were probed for G or Giα2. Glutathione S-transferase (GST) reprobe indicated the equal loading. n = 2. (Aii) Human platelet lysate from resting or 1 U/mL thrombin-stimulated platelets in the presence or absence of GDP+AlF4 were subjected to immunoprecipitation of GRK2 and probed for Gq. n = 3. (B) GRK2 from resting and thrombin-stimulated (1 U/mL) human platelet lysate was immunoprecipitated with the specific mouse anti-GRK2 antibody and probed for Gβ. GRK2 was reprobed with an anti-GRK2 antibody. n = 6. A marker line was excised as indicated by the vertical line.

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