BD PharmingenTM PE Mouse Anti-Human Platelet GPVI

Description

Flow cytometric analysis of Platelet GPVI expression on human peripheral blood platelets. Platelets were isolated from fresh whole blood and fixed with BD Cytofix Fixation Buffer Cat. No. 554655 . After washing, the fixed platelets were stained with PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dashed line histogram or PE Mouse Anti-Human Platelet GPVI antibody Cat. No. 565241; solid line histogram . The fluorescence histogram showing GPVI expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of intact platelets. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of Platelet GPVI expression on human peripheral blood platelets. Platelets were isolated from fresh whole blood and fixed with BD Cytofix Fixation Buffer Cat. No. 554655 . After washing, the fixed platelets were stained with PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dashed line histogram or PE Mouse Anti-Human Platelet GPVI antibody Cat. No. 565241; solid line histogram . The fluorescence histogram showing GPVI expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of intact platelets. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of Platelet GPVI expression on human peripheral blood platelets. Platelets were isolated from fresh whole blood and fixed with BD Cytofix Fixation Buffer Cat. No. 554655 . After washing, the fixed platelets were stained with PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dashed line histogram or PE Mouse Anti-Human Platelet GPVI antibody Cat. No. 565241; solid line histogram . The fluorescence histogram showing GPVI expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of intact platelets. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System.