BD PharmingenTM Alexa Fluor 647 Mouse Anti-Human CD263 (TRAIL-R3)

Description

Two-parameter flow cytometric analysis of CD263 TRAIL-R3 expression on human peripheral blood leucocyte populations. Whole blood cells were stained with either Alexa Fluor 647 Mouse IgG1, kappa Isotype Control Cat. No. 557714, Left Panel or Alexa Fluor 647 Mouse anti-Human CD263 antibody Cat. No. 565458; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-parameter flow cytometric contour plots showing the correlated expression of CD263 TRAIL-R3 or Ig Isotype control staining versus Side Light-scatter SSC signals were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometric analysis was performed using a BD Canto II Flow Cytometer System. Two-parameter flow cytometric analysis of CD263 TRAIL-R3 expression on human peripheral blood leucocyte populations. Whole blood cells were stained with either Alexa Fluor 647 Mouse IgG1, kappa Isotype Control Cat. No. 557714, Left Panel or Alexa Fluor 647 Mouse anti-Human CD263 antibody Cat. No. 565458; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-parameter flow cytometric contour plots showing the correlated expression of CD263 TRAIL-R3 or Ig Isotype control staining versus Side Light-scatter SSC signals were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometric analysis was performed using a BD Canto II Flow Cytometer System. Two-parameter flow cytometric analysis of CD263 TRAIL-R3 expression on human peripheral blood leucocyte populations. Whole blood cells were stained with either Alexa Fluor 647 Mouse IgG1, kappa Isotype Control Cat. No. 557714, Left Panel or Alexa Fluor 647 Mouse anti-Human CD263 antibody Cat. No. 565458; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-parameter flow cytometric contour plots showing the correlated expression of CD263 TRAIL-R3 or Ig Isotype control staining versus Side Light-scatter SSC signals were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometric analysis was performed using a BD Canto II Flow Cytometer System. Show More Two-parameter flow cytometric analysis of CD263 TRAIL-R3 expression on human peripheral blood leucocyte populations. Whole blood cells were stained with either Alexa Fluor 647 Mouse IgG1, kappa Isotype Control Cat. No. 557714, Left Panel or Alexa Fluor 647 Mouse anti-Human CD263 antibody Cat. No. 565458; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-parameter flow cytometric contour plots showing the correlated expression of CD263 TRAIL-R3 or Ig Isotype control staining versus Side Light-scatter SSC signals were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometric analysis was performed using a BD Canto II Flow Cytometer System. Show More Two-parameter flow cytometric analysis of CD263 TRAIL-R3 expression on human peripheral blood leucocyte populations. Whole blood cells were stained with either Alexa Fluor 647 Mouse IgG1, kappa Isotype Control Cat. No. 557714, Left Panel or Alexa Fluor 647 Mouse anti-Human CD263 antibody Cat. No. 565458; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-parameter flow cytometric contour plots showing the correlated expression of CD263 TRAIL-R3 or Ig Isotype control staining versus Side Light-scatter SSC signals were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometric analysis was performed using a BD Canto II Flow Cytometer System. Two-parameter flow cytometric analysis of CD263 TRAIL-R3 expression on human peripheral blood leucocyte populations. Whole blood cells were stained with either Alexa Fluor 647 Mouse IgG1, kappa Isotype Control Cat. No. 557714, Left Panel or Alexa Fluor 647 Mouse anti-Human CD263 antibody Cat. No. 565458; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-parameter flow cytometric contour plots showing the correlated expression of CD263 TRAIL-R3 or Ig Isotype control staining versus Side Light-scatter SSC signals were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometric analysis was performed using a BD Canto II Flow Cytometer System.