BD PharmingenTM PE Mouse Anti-Human CD65

Description

Multiparameter flow cytometric analysis of CD65 expression on Human peripheral blood leucocytes. Human whole blood cells were stained with either PE Mouse IgM Isotype Control Cat. No. 555584; Left Plot or PE Mouse Anti-Human CD65 antibody Cat. No. 565858 . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD65 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 LSRFortessa Cell Analyzer System. Multiparameter flow cytometric analysis of CD65 expression on Human peripheral blood leucocytes. Human whole blood cells were stained with either PE Mouse IgM Isotype Control Cat. No. 555584; Left Plot or PE Mouse Anti-Human CD65 antibody Cat. No. 565858 . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD65 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 LSRFortessa Cell Analyzer System. Multiparameter flow cytometric analysis of CD65 expression on Human peripheral blood leucocytes. Human whole blood cells were stained with either PE Mouse IgM Isotype Control Cat. No. 555584; Left Plot or PE Mouse Anti-Human CD65 antibody Cat. No. 565858 . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD65 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 LSRFortessa Cell Analyzer System. Show More Multiparameter flow cytometric analysis of CD65 expression on Human peripheral blood leucocytes. Human whole blood cells were stained with either PE Mouse IgM Isotype Control Cat. No. 555584; Left Plot or PE Mouse Anti-Human CD65 antibody Cat. No. 565858 . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD65 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 LSRFortessa Cell Analyzer System. Show More Multiparameter flow cytometric analysis of CD65 expression on Human peripheral blood leucocytes. Human whole blood cells were stained with either PE Mouse IgM Isotype Control Cat. No. 555584; Left Plot or PE Mouse Anti-Human CD65 antibody Cat. No. 565858 . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD65 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 LSRFortessa Cell Analyzer System. Multiparameter flow cytometric analysis of CD65 expression on Human peripheral blood leucocytes. Human whole blood cells were stained with either PE Mouse IgM Isotype Control Cat. No. 555584; Left Plot or PE Mouse Anti-Human CD65 antibody Cat. No. 565858 . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Two-parameter flow cytometric contour plots showing the correlated expression of CD65 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 LSRFortessa Cell Analyzer System.