BD PharmingenTM Alexa Fluor 647 Rat Anti-Mouse CD62P

Description

Flow cytometric analysis of CD62P expression on mouse platelets. Mouse platelets were either not activated Left Panel or activated with human thrombin Sigma T-8885; 20 U/ml final concentration; 5 min at 37C; Right Panel . The platelets were stained with either Alexa Fluor 647 Rat IgG1, lambda Isotype Control Cat. No. 563713; dashed line histograms or Alexa Fluor 647 Rat Anti-Mouse CD62P antibody Cat. No. 563674; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of platelets. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD62P expression on mouse platelets. Mouse platelets were either not activated Left Panel or activated with human thrombin Sigma T-8885; 20 U/ml final concentration; 5 min at 37C; Right Panel . The platelets were stained with either Alexa Fluor 647 Rat IgG1, lambda Isotype Control Cat. No. 563713; dashed line histograms or Alexa Fluor 647 Rat Anti-Mouse CD62P antibody Cat. No. 563674; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of platelets. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD62P expression on mouse platelets. Mouse platelets were either not activated Left Panel or activated with human thrombin Sigma T-8885; 20 U/ml final concentration; 5 min at 37C; Right Panel . The platelets were stained with either Alexa Fluor 647 Rat IgG1, lambda Isotype Control Cat. No. 563713; dashed line histograms or Alexa Fluor 647 Rat Anti-Mouse CD62P antibody Cat. No. 563674; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of platelets. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD62P expression on mouse platelets. Mouse platelets were either not activated Left Panel or activated with human thrombin Sigma T-8885; 20 U/ml final concentration; 5 min at 37C; Right Panel . The platelets were stained with either Alexa Fluor 647 Rat IgG1, lambda Isotype Control Cat. No. 563713; dashed line histograms or Alexa Fluor 647 Rat Anti-Mouse CD62P antibody Cat. No. 563674; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of platelets. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD62P expression on mouse platelets. Mouse platelets were either not activated Left Panel or activated with human thrombin Sigma T-8885; 20 U/ml final concentration; 5 min at 37C; Right Panel . The platelets were stained with either Alexa Fluor 647 Rat IgG1, lambda Isotype Control Cat. No. 563713; dashed line histograms or Alexa Fluor 647 Rat Anti-Mouse CD62P antibody Cat. No. 563674; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of platelets. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD62P expression on mouse platelets. Mouse platelets were either not activated Left Panel or activated with human thrombin Sigma T-8885; 20 U/ml final concentration; 5 min at 37C; Right Panel . The platelets were stained with either Alexa Fluor 647 Rat IgG1, lambda Isotype Control Cat. No. 563713; dashed line histograms or Alexa Fluor 647 Rat Anti-Mouse CD62P antibody Cat. No. 563674; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of platelets. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System.