BD PharmingenTM APC Hamster Anti-Mouse CD279 (PD-1)

Description

Flow cytometric analysis of CD279 PD-1 expression on mouse resting and activated splenocytes. Splenocytes from C57BL/6 mouse were activated by culture with plate-bound NA/LE Hamster Anti-Mouse CD3 antibody Cat. No. 553057 for 3 days. The resting Left Panel or activated splenocytes Right Panel were stained either with APC Hamster IgG2, kappa Isotype Control Cat. No. 562169; dashed line histogram or with the APC Hamster Anti-Mouse CD279 PD-1 antibody Cat. No. 562671; 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 mouse resting and activated splenocytes. Splenocytes from C57BL/6 mouse were activated by culture with plate-bound NA/LE Hamster Anti-Mouse CD3 antibody Cat. No. 553057 for 3 days. The resting Left Panel or activated splenocytes Right Panel were stained either with APC Hamster IgG2, kappa Isotype Control Cat. No. 562169; dashed line histogram or with the APC Hamster Anti-Mouse CD279 PD-1 antibody Cat. No. 562671; 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 mouse resting and activated splenocytes. Splenocytes from C57BL/6 mouse were activated by culture with plate-bound NA/LE Hamster Anti-Mouse CD3 antibody Cat. No. 553057 for 3 days. The resting Left Panel or activated splenocytes Right Panel were stained either with APC Hamster IgG2, kappa Isotype Control Cat. No. 562169; dashed line histogram or with the APC Hamster Anti-Mouse CD279 PD-1 antibody Cat. No. 562671; 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 mouse resting and activated splenocytes. Splenocytes from C57BL/6 mouse were activated by culture with plate-bound NA/LE Hamster Anti-Mouse CD3 antibody Cat. No. 553057 for 3 days. The resting Left Panel or activated splenocytes Right Panel were stained either with APC Hamster IgG2, kappa Isotype Control Cat. No. 562169; dashed line histogram or with the APC Hamster Anti-Mouse CD279 PD-1 antibody Cat. No. 562671; 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 mouse resting and activated splenocytes. Splenocytes from C57BL/6 mouse were activated by culture with plate-bound NA/LE Hamster Anti-Mouse CD3 antibody Cat. No. 553057 for 3 days. The resting Left Panel or activated splenocytes Right Panel were stained either with APC Hamster IgG2, kappa Isotype Control Cat. No. 562169; dashed line histogram or with the APC Hamster Anti-Mouse CD279 PD-1 antibody Cat. No. 562671; 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 mouse resting and activated splenocytes. Splenocytes from C57BL/6 mouse were activated by culture with plate-bound NA/LE Hamster Anti-Mouse CD3 antibody Cat. No. 553057 for 3 days. The resting Left Panel or activated splenocytes Right Panel were stained either with APC Hamster IgG2, kappa Isotype Control Cat. No. 562169; dashed line histogram or with the APC Hamster Anti-Mouse CD279 PD-1 antibody Cat. No. 562671; 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.