BD PharmingenTM PE Mouse Anti-Human CD31

Description

Flow cytometric analysis of human CD31 expression on human peripheral blood leucocytes. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No.554680; dashed line histograms or PE Mouse Anti-Human CD31 antibody Cat. No. 566125/566177; solid line histograms . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 .The fluorescence histograms showing CD31 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable monocytes Left Panel or granulocytes Right Panel . Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Flow cytometric analysis of human CD31 expression on human peripheral blood leucocytes. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No.554680; dashed line histograms or PE Mouse Anti-Human CD31 antibody Cat. No. 566125/566177; solid line histograms . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 .The fluorescence histograms showing CD31 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable monocytes Left Panel or granulocytes Right Panel . Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Flow cytometric analysis of human CD31 expression on human peripheral blood leucocytes. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No.554680; dashed line histograms or PE Mouse Anti-Human CD31 antibody Cat. No. 566125/566177; solid line histograms . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 .The fluorescence histograms showing CD31 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable monocytes Left Panel or granulocytes Right Panel . Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Show More Flow cytometric analysis of human CD31 expression on human peripheral blood leucocytes. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No.554680; dashed line histograms or PE Mouse Anti-Human CD31 antibody Cat. No. 566125/566177; solid line histograms . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 .The fluorescence histograms showing CD31 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable monocytes Left Panel or granulocytes Right Panel . Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Show More Flow cytometric analysis of human CD31 expression on human peripheral blood leucocytes. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No.554680; dashed line histograms or PE Mouse Anti-Human CD31 antibody Cat. No. 566125/566177; solid line histograms . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 .The fluorescence histograms showing CD31 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable monocytes Left Panel or granulocytes Right Panel . Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Flow cytometric analysis of human CD31 expression on human peripheral blood leucocytes. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No.554680; dashed line histograms or PE Mouse Anti-Human CD31 antibody Cat. No. 566125/566177; solid line histograms . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 .The fluorescence histograms showing CD31 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable monocytes Left Panel or granulocytes Right Panel . Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System.