BD PharmingenTM PE Mouse Anti-Human CD282

Description

Two-parameter flow cytometric analysis of CD282 TLR2 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 CD282 antibody Cat. No. 565349; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD282 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. Two-parameter flow cytometric analysis of CD282 TLR2 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 CD282 antibody Cat. No. 565349; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD282 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. Two-parameter flow cytometric analysis of CD282 TLR2 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 CD282 antibody Cat. No. 565349; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD282 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 Two-parameter flow cytometric analysis of CD282 TLR2 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 CD282 antibody Cat. No. 565349; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD282 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 Two-parameter flow cytometric analysis of CD282 TLR2 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 CD282 antibody Cat. No. 565349; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD282 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. Two-parameter flow cytometric analysis of CD282 TLR2 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 CD282 antibody Cat. No. 565349; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD282 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.