BD PharmingenTM FITC Mouse Anti-Human CD65

Description

Multiparameter flow cytometric analysis of CD65 expression on Human peripheral blood leukocyte populations. Human whole blood was first treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes, washed, and then preincubated with BD Pharmingen Human BD Fc Block Cat. No. 564219/564220 . The leukocytes were then stained with either FITC Mouse IgM, kappa Isotype Control Cat. No. 553474; Left Plot or FITC Mouse Anti-Human CD65 antibody Cat. No. 569474/569475 . The bivariate pseudocolor density plot showing the correlated expression CD65 or Ig Isotype control staining versus side light-scatter SSC-A signals was derived from gated events with the forward and side light-scatter characteristics of viable leukocytes. Flow cytometry and data analysis were performed using a BD FACSymphony A5 SE Cell Analyzer System and FlowJo software. Multiparameter flow cytometric analysis of CD65 expression on Human peripheral blood leukocyte populations. Human whole blood was first treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes, washed, and then preincubated with BD Pharmingen Human BD Fc Block Cat. No. 564219/564220 . The leukocytes were then stained with either FITC Mouse IgM, kappa Isotype Control Cat. No. 553474; Left Plot or FITC Mouse Anti-Human CD65 antibody Cat. No. 569474/569475 . The bivariate pseudocolor density plot showing the correlated expression CD65 or Ig Isotype control staining versus side light-scatter SSC-A signals was derived from gated events with the forward and side light-scatter characteristics of viable leukocytes. Flow cytometry and data analysis were performed using a BD FACSymphony A5 SE Cell Analyzer System and FlowJo software. Multiparameter flow cytometric analysis of CD65 expression on Human peripheral blood leukocyte populations. Human whole blood was first treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes, washed, and then preincubated with BD Pharmingen Human BD Fc Block Cat. No. 564219/564220 . The leukocytes were then stained with either FITC Mouse IgM, kappa Isotype Control Cat. No. 553474; Left Plot or FITC Mouse Anti-Human CD65 antibody Cat. No. 569474/569475 . The bivariate pseudocolor density plot showing the correlated expression CD65 or Ig Isotype control staining versus side light-scatter SSC-A signals was derived from gated events with the forward and side light-scatter characteristics of viable leukocytes. Flow cytometry and data analysis were performed using a BD FACSymphony A5 SE Cell Analyzer System and FlowJo software. Show More Multiparameter flow cytometric analysis of CD65 expression on Human peripheral blood leukocyte populations. Human whole blood was first treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes, washed, and then preincubated with BD Pharmingen Human BD Fc Block Cat. No. 564219/564220 . The leukocytes were then stained with either FITC Mouse IgM, kappa Isotype Control Cat. No. 553474; Left Plot or FITC Mouse Anti-Human CD65 antibody Cat. No. 569474/569475 . The bivariate pseudocolor density plot showing the correlated expression CD65 or Ig Isotype control staining versus side light-scatter SSC-A signals was derived from gated events with the forward and side light-scatter characteristics of viable leukocytes. Flow cytometry and data analysis were performed using a BD FACSymphony A5 SE Cell Analyzer System and FlowJo software. Show More Multiparameter flow cytometric analysis of CD65 expression on Human peripheral blood leukocyte populations. Human whole blood was first treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes, washed, and then preincubated with BD Pharmingen Human BD Fc Block Cat. No. 564219/564220 . The leukocytes were then stained with either FITC Mouse IgM, kappa Isotype Control Cat. No. 553474; Left Plot or FITC Mouse Anti-Human CD65 antibody Cat. No. 569474/569475 . The bivariate pseudocolor density plot showing the correlated expression CD65 or Ig Isotype control staining versus side light-scatter SSC-A signals was derived from gated events with the forward and side light-scatter characteristics of viable leukocytes. Flow cytometry and data analysis were performed using a BD FACSymphony A5 SE Cell Analyzer System and FlowJo software. Multiparameter flow cytometric analysis of CD65 expression on Human peripheral blood leukocyte populations. Human whole blood was first treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes, washed, and then preincubated with BD Pharmingen Human BD Fc Block Cat. No. 564219/564220 . The leukocytes were then stained with either FITC Mouse IgM, kappa Isotype Control Cat. No. 553474; Left Plot or FITC Mouse Anti-Human CD65 antibody Cat. No. 569474/569475 . The bivariate pseudocolor density plot showing the correlated expression CD65 or Ig Isotype control staining versus side light-scatter SSC-A signals was derived from gated events with the forward and side light-scatter characteristics of viable leukocytes. Flow cytometry and data analysis were performed using a BD FACSymphony A5 SE Cell Analyzer System and FlowJo software.