BD PharmingenTM PE Mouse Anti-Human CD229

Description

Multiparameter flow cytometric analysis of CD229 expression on human peripheral blood leucocytes. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; Left Panel or PE Mouse Anti-Human CD229 antibody Cat. No. 565238; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD229 or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from gated events with the forward and side light-scatter characteristics of intact leucocyte populations. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Multiparameter flow cytometric analysis of CD229 expression on human peripheral blood leucocytes. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; Left Panel or PE Mouse Anti-Human CD229 antibody Cat. No. 565238; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD229 or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from gated events with the forward and side light-scatter characteristics of intact leucocyte populations. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Multiparameter flow cytometric analysis of CD229 expression on human peripheral blood leucocytes. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; Left Panel or PE Mouse Anti-Human CD229 antibody Cat. No. 565238; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD229 or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from gated events with the forward and side light-scatter characteristics of intact leucocyte populations. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Multiparameter flow cytometric analysis of CD229 expression on human peripheral blood leucocytes. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; Left Panel or PE Mouse Anti-Human CD229 antibody Cat. No. 565238; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD229 or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from gated events with the forward and side light-scatter characteristics of intact leucocyte populations. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Multiparameter flow cytometric analysis of CD229 expression on human peripheral blood leucocytes. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; Left Panel or PE Mouse Anti-Human CD229 antibody Cat. No. 565238; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD229 or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from gated events with the forward and side light-scatter characteristics of intact leucocyte populations. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Multiparameter flow cytometric analysis of CD229 expression on human peripheral blood leucocytes. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; Left Panel or PE Mouse Anti-Human CD229 antibody Cat. No. 565238; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD229 or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from gated events with the forward and side light-scatter characteristics of intact leucocyte populations. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System.