BD PharmingenTM PE Mouse Anti-Human CD1c

Description

Two-color flow cytometric analysis of CD1c expression on human peripheral blood lymphocytes. Human whole blood was treated with BD Pharm Lyse Cat. No. 555899 to lyse erythrocytes. The leucocytes were stained with BD Horizon V450 Mouse Anti-Human CD19 antibody Cat. No. 560353/560354 and either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; Left Panel or PE Mouse Anti-Human CD1c Cat. No. 564900; Right Panel . Two-color contour plots showing the correlated expression of CD19 versus CD1c or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Two-color flow cytometric analysis of CD1c expression on human peripheral blood lymphocytes. Human whole blood was treated with BD Pharm Lyse Cat. No. 555899 to lyse erythrocytes. The leucocytes were stained with BD Horizon V450 Mouse Anti-Human CD19 antibody Cat. No. 560353/560354 and either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; Left Panel or PE Mouse Anti-Human CD1c Cat. No. 564900; Right Panel . Two-color contour plots showing the correlated expression of CD19 versus CD1c or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Two-color flow cytometric analysis of CD1c expression on human peripheral blood lymphocytes. Human whole blood was treated with BD Pharm Lyse Cat. No. 555899 to lyse erythrocytes. The leucocytes were stained with BD Horizon V450 Mouse Anti-Human CD19 antibody Cat. No. 560353/560354 and either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; Left Panel or PE Mouse Anti-Human CD1c Cat. No. 564900; Right Panel . Two-color contour plots showing the correlated expression of CD19 versus CD1c or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Show More Two-color flow cytometric analysis of CD1c expression on human peripheral blood lymphocytes. Human whole blood was treated with BD Pharm Lyse Cat. No. 555899 to lyse erythrocytes. The leucocytes were stained with BD Horizon V450 Mouse Anti-Human CD19 antibody Cat. No. 560353/560354 and either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; Left Panel or PE Mouse Anti-Human CD1c Cat. No. 564900; Right Panel . Two-color contour plots showing the correlated expression of CD19 versus CD1c or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Show More Two-color flow cytometric analysis of CD1c expression on human peripheral blood lymphocytes. Human whole blood was treated with BD Pharm Lyse Cat. No. 555899 to lyse erythrocytes. The leucocytes were stained with BD Horizon V450 Mouse Anti-Human CD19 antibody Cat. No. 560353/560354 and either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; Left Panel or PE Mouse Anti-Human CD1c Cat. No. 564900; Right Panel . Two-color contour plots showing the correlated expression of CD19 versus CD1c or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Two-color flow cytometric analysis of CD1c expression on human peripheral blood lymphocytes. Human whole blood was treated with BD Pharm Lyse Cat. No. 555899 to lyse erythrocytes. The leucocytes were stained with BD Horizon V450 Mouse Anti-Human CD19 antibody Cat. No. 560353/560354 and either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; Left Panel or PE Mouse Anti-Human CD1c Cat. No. 564900; Right Panel . Two-color contour plots showing the correlated expression of CD19 versus CD1c or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System.