BD HorizonTM BV711 Hamster Anti-Rat/Mouse CD49a

Description

Flow cytometric analysis of mouse CD49a expression on C1300 cells. Cells from the C1300 mouse neuroblastoma cell line were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 . The cells were then stained with either BD Horizon BV711 Armenian Hamster IgG2, lambda1 Isotype Control Cat. No. 563348; dashed line histogram or BD Horizon BV711 Hamster Anti-Rat/Mouse CD49a antibody Cat. No. 564863; solid line histogram . The fluorescence histogram showing CD49a expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of mouse CD49a expression on C1300 cells. Cells from the C1300 mouse neuroblastoma cell line were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 . The cells were then stained with either BD Horizon BV711 Armenian Hamster IgG2, lambda1 Isotype Control Cat. No. 563348; dashed line histogram or BD Horizon BV711 Hamster Anti-Rat/Mouse CD49a antibody Cat. No. 564863; solid line histogram . The fluorescence histogram showing CD49a expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of mouse CD49a expression on C1300 cells. Cells from the C1300 mouse neuroblastoma cell line were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 . The cells were then stained with either BD Horizon BV711 Armenian Hamster IgG2, lambda1 Isotype Control Cat. No. 563348; dashed line histogram or BD Horizon BV711 Hamster Anti-Rat/Mouse CD49a antibody Cat. No. 564863; solid line histogram . The fluorescence histogram showing CD49a expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System.