Fig. 3.
Fig. 3. ADP-ribosylation of RhoA in platelets by C3 exoenzyme. In (A) washed platelets were incubated for 4 hours at 37°C in the presence of vehicle buffer (“No C3”) or C3 exoenzyme. The platelets were then washed and subjected to α(32P)ADP-ribosylation assay as described in Materials and Methods. In (B) the solid bars represent the means ± SEM of three experiments.

ADP-ribosylation of RhoA in platelets by C3 exoenzyme. In (A) washed platelets were incubated for 4 hours at 37°C in the presence of vehicle buffer (“No C3”) or C3 exoenzyme. The platelets were then washed and subjected to α(32P)ADP-ribosylation assay as described in Materials and Methods. In (B) the solid bars represent the means ± SEM of three experiments.

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