Fig. 7.
Fig. 7. Enrichment of stomatin in microvesicles after platelet activation. / Platelets (1 × 109 cells/mL) were activated by incubation with 4 μM ionophore A23187 (A) or 1 U/mL thrombin (B) at 37°C for 30 minutes. Platelets and microvesicles were isolated by differential pelleting steps, and aliquots normalized to equal protein content were analyzed by Western blotting. Representative data are shown (n = 3); pl indicates platelets; and mv, microvesicles.

Enrichment of stomatin in microvesicles after platelet activation.

Platelets (1 × 109 cells/mL) were activated by incubation with 4 μM ionophore A23187 (A) or 1 U/mL thrombin (B) at 37°C for 30 minutes. Platelets and microvesicles were isolated by differential pelleting steps, and aliquots normalized to equal protein content were analyzed by Western blotting. Representative data are shown (n = 3); pl indicates platelets; and mv, microvesicles.

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