BD HorizonTM BV421 Hamster Anti-Mouse CD279 (PD-1)

Description

Flow cytometric analysis of CD279 PD-1 expression on resting and activated mouse splenocytes. Splenocytes from a C57BL/6 mouse were activated in culture with plate-bound Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 for 3 days. The resting Left Panel or activated Right Panel splenocytes were stained with either a BD Horizon BV421 Hamster IgG2, kappa isotype control Cat. No. 562612; dashed line histogram or with the BD Horizon BV421 Hamster Anti-Mouse CD279 PD-1 antibody Cat. No. 562584/565942; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD279 PD-1 expression on resting and activated mouse splenocytes. Splenocytes from a C57BL/6 mouse were activated in culture with plate-bound Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 for 3 days. The resting Left Panel or activated Right Panel splenocytes were stained with either a BD Horizon BV421 Hamster IgG2, kappa isotype control Cat. No. 562612; dashed line histogram or with the BD Horizon BV421 Hamster Anti-Mouse CD279 PD-1 antibody Cat. No. 562584/565942; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD279 PD-1 expression on resting and activated mouse splenocytes. Splenocytes from a C57BL/6 mouse were activated in culture with plate-bound Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 for 3 days. The resting Left Panel or activated Right Panel splenocytes were stained with either a BD Horizon BV421 Hamster IgG2, kappa isotype control Cat. No. 562612; dashed line histogram or with the BD Horizon BV421 Hamster Anti-Mouse CD279 PD-1 antibody Cat. No. 562584/565942; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD279 PD-1 expression on resting and activated mouse splenocytes. Splenocytes from a C57BL/6 mouse were activated in culture with plate-bound Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 for 3 days. The resting Left Panel or activated Right Panel splenocytes were stained with either a BD Horizon BV421 Hamster IgG2, kappa isotype control Cat. No. 562612; dashed line histogram or with the BD Horizon BV421 Hamster Anti-Mouse CD279 PD-1 antibody Cat. No. 562584/565942; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD279 PD-1 expression on resting and activated mouse splenocytes. Splenocytes from a C57BL/6 mouse were activated in culture with plate-bound Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 for 3 days. The resting Left Panel or activated Right Panel splenocytes were stained with either a BD Horizon BV421 Hamster IgG2, kappa isotype control Cat. No. 562612; dashed line histogram or with the BD Horizon BV421 Hamster Anti-Mouse CD279 PD-1 antibody Cat. No. 562584/565942; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD279 PD-1 expression on resting and activated mouse splenocytes. Splenocytes from a C57BL/6 mouse were activated in culture with plate-bound Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 for 3 days. The resting Left Panel or activated Right Panel splenocytes were stained with either a BD Horizon BV421 Hamster IgG2, kappa isotype control Cat. No. 562612; dashed line histogram or with the BD Horizon BV421 Hamster Anti-Mouse CD279 PD-1 antibody Cat. No. 562584/565942; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System.