BD PharmingenTM PE Mouse Anti-Human CD272 (BTLA)

Description

Two-color flow cytometric analysis of CD272 BTLA on human peripheral blood lymphocytes. Human whole blood was stained with FITC Mouse Anti-Human CD3 antibody Cat. No. 555332/561806/561807 and either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; Left Panel or PE Mouse Anti-Human CD272 BTLA Cat. No. 558485, Right Panel . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-color flow cytometric dot plots showing the correlated expression of CD3 versus CD272 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 FACSCalibur System. Two-color flow cytometric analysis of CD272 BTLA on human peripheral blood lymphocytes. Human whole blood was stained with FITC Mouse Anti-Human CD3 antibody Cat. No. 555332/561806/561807 and either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; Left Panel or PE Mouse Anti-Human CD272 BTLA Cat. No. 558485, Right Panel . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-color flow cytometric dot plots showing the correlated expression of CD3 versus CD272 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 FACSCalibur System. Show More Two-color flow cytometric analysis of CD272 BTLA on human peripheral blood lymphocytes. Human whole blood was stained with FITC Mouse Anti-Human CD3 antibody Cat. No. 555332/561806/561807 and either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; Left Panel or PE Mouse Anti-Human CD272 BTLA Cat. No. 558485, Right Panel . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-color flow cytometric dot plots showing the correlated expression of CD3 versus CD272 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 FACSCalibur System.