Figure 6
Figure 6. Platelets null for PRKAR2B are hyporesponsive. (A) PRKAR2B immunoblot. Lysates of mouse wild-type (wt) brain, wt platelets, and platelets from Prkar2b−/− mice (KO) were subjected to sodium dodecyl sulfate–polyacrylamide gel electrophoresis and immunoblotted with polyclonal antisera raised against recombinant mouse protein as described.29 Approximately equal loading is shown by immunoblotting for β-actin. (B) Platelet surface expression of the activation marker, P-selectin, was quantified by flow cytometry on platelets from wild-type (WT) mice and mice null for Prkar2b (KO).29 Platelets were stimulated with a fixed, subthreshold concentration of PAR4AP (0.8mM) and the indicated increasing concentrations of epinephrine.

Platelets null for PRKAR2B are hyporesponsive. (A) PRKAR2B immunoblot. Lysates of mouse wild-type (wt) brain, wt platelets, and platelets from Prkar2b−/− mice (KO) were subjected to sodium dodecyl sulfate–polyacrylamide gel electrophoresis and immunoblotted with polyclonal antisera raised against recombinant mouse protein as described.29  Approximately equal loading is shown by immunoblotting for β-actin. (B) Platelet surface expression of the activation marker, P-selectin, was quantified by flow cytometry on platelets from wild-type (WT) mice and mice null for Prkar2b (KO).29  Platelets were stimulated with a fixed, subthreshold concentration of PAR4AP (0.8mM) and the indicated increasing concentrations of epinephrine.

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