BD HorizonTM BV421 Mouse Anti-Human CD40

Description

Two-color flow cytometric analysis of CD40 expression on human peripheral blood lymphocytes. Whole blood was stained with APC Mouse Anti-Human CD19 antibody Cat. No. 555415/561742 and either BD Horizon BV421 Mouse IgG1, kappa Isotype Control Cat. No. 562438; Left Panel or BD Horizon BV421 Mouse Anti-Human CD40 antibody Cat. No. 563396; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Flow cytometric dot plots showing correlated expression of CD40 or Ig Isotype control staining versus CD19 were derived from events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Two-color flow cytometric analysis of CD40 expression on human peripheral blood lymphocytes. Whole blood was stained with APC Mouse Anti-Human CD19 antibody Cat. No. 555415/561742 and either BD Horizon BV421 Mouse IgG1, kappa Isotype Control Cat. No. 562438; Left Panel or BD Horizon BV421 Mouse Anti-Human CD40 antibody Cat. No. 563396; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Flow cytometric dot plots showing correlated expression of CD40 or Ig Isotype control staining versus CD19 were derived from events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Two-color flow cytometric analysis of CD40 expression on human peripheral blood lymphocytes. Whole blood was stained with APC Mouse Anti-Human CD19 antibody Cat. No. 555415/561742 and either BD Horizon BV421 Mouse IgG1, kappa Isotype Control Cat. No. 562438; Left Panel or BD Horizon BV421 Mouse Anti-Human CD40 antibody Cat. No. 563396; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Flow cytometric dot plots showing correlated expression of CD40 or Ig Isotype control staining versus CD19 were derived from events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Two-color flow cytometric analysis of CD40 expression on human peripheral blood lymphocytes. Whole blood was stained with APC Mouse Anti-Human CD19 antibody Cat. No. 555415/561742 and either BD Horizon BV421 Mouse IgG1, kappa Isotype Control Cat. No. 562438; Left Panel or BD Horizon BV421 Mouse Anti-Human CD40 antibody Cat. No. 563396; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Flow cytometric dot plots showing correlated expression of CD40 or Ig Isotype control staining versus CD19 were derived from events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Two-color flow cytometric analysis of CD40 expression on human peripheral blood lymphocytes. Whole blood was stained with APC Mouse Anti-Human CD19 antibody Cat. No. 555415/561742 and either BD Horizon BV421 Mouse IgG1, kappa Isotype Control Cat. No. 562438; Left Panel or BD Horizon BV421 Mouse Anti-Human CD40 antibody Cat. No. 563396; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Flow cytometric dot plots showing correlated expression of CD40 or Ig Isotype control staining versus CD19 were derived from events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Two-color flow cytometric analysis of CD40 expression on human peripheral blood lymphocytes. Whole blood was stained with APC Mouse Anti-Human CD19 antibody Cat. No. 555415/561742 and either BD Horizon BV421 Mouse IgG1, kappa Isotype Control Cat. No. 562438; Left Panel or BD Horizon BV421 Mouse Anti-Human CD40 antibody Cat. No. 563396; Right Panel . Erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . Flow cytometric dot plots showing correlated expression of CD40 or Ig Isotype control staining versus CD19 were derived from events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System.