Fig. 3.
Fig. 3. Flow cytometry analysis of platelets treated with or without MβCD for surface GPVI and the integrins αIIbβ3 and α2. / Platelets were incubated with 0 (−) or 20 mM (+)MβCD for 30 minutes, washed once, and resuspended in HEPES buffer. (A) Cells were stained with F(ab′)2 fragments of human anti-GPVI IgG or those of control IgG followed by FITC-labeled antihuman IgG antibody and were analyzed by flow cytometry. (B) Cells were stained with anti-αIIbβ3 antibody (P2), anti-α2 antibody (Gi9), or mouse IgG1 as a negative control followed by FITC-labeled antimouse IgG antibody and were analyzed by flow cytometry.

Flow cytometry analysis of platelets treated with or without MβCD for surface GPVI and the integrins αIIbβ3 and α2.

Platelets were incubated with 0 (−) or 20 mM (+)MβCD for 30 minutes, washed once, and resuspended in HEPES buffer. (A) Cells were stained with F(ab′)2 fragments of human anti-GPVI IgG or those of control IgG followed by FITC-labeled antihuman IgG antibody and were analyzed by flow cytometry. (B) Cells were stained with anti-αIIbβ3 antibody (P2), anti-α2 antibody (Gi9), or mouse IgG1 as a negative control followed by FITC-labeled antimouse IgG antibody and were analyzed by flow cytometry.

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