
569780 ·
BDB Bioscience · Cat: 569780
Reach 3+ verified distributors
Manufacturer product page
bdbiosciences.com/en-us/products/reagents/flow-cytometry-rea...
Description
Flow cytometric analysis of CD279 PD-1 expression on resting and activated Mouse splenic leukocytes. C57BL/6 Mouse splenocytes were cultured with plate-bound Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 for 3 days. The resting Left Plot or activated Right Plot splenocytes were harvested, preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 , and then stained with either BD Horizon BV421 Rat IgG2b, kappa Isotype Control Cat. No. 562603; dashed line histograms or BD Horizon BV421 Rat Anti-Mouse CD279 PD-1 antibody Cat. No. 569780; solid line histograms at 0.5 mug/test. BD Via-Probe Cell Viability 7-AAD Solution Cat. No. 555815/555816 was added to cells right before analysis. The fluorescence histograms showing CD279 PD-1 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable 7-AAD-negative splenic leukocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Data shown on this Technical Data Sheet are not lot specific. Flow cytometric analysis of CD279 PD-1 expression on resting and activated Mouse splenic leukocytes. C57BL/6 Mouse splenocytes were cultured with plate-bound Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 for 3 days. The resting Left Plot or activated Right Plot splenocytes were harvested, preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 , and then stained with either BD Horizon BV421 Rat IgG2b, kappa Isotype Control Cat. No. 562603; dashed line histograms or BD Horizon BV421 Rat Anti-Mouse CD279 PD-1 antibody Cat. No. 569780; solid line histograms at 0.5 mug/test. BD Via-Probe Cell Viability 7-AAD Solution Cat. No. 555815/555816 was added to cells right before analysis. The fluorescence histograms showing CD279 PD-1 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable 7-AAD-negative splenic leukocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Data shown on this Technical Data Sheet are not lot specific. Flow cytometric analysis of CD279 PD-1 expression on resting and activated Mouse splenic leukocytes. C57BL/6 Mouse splenocytes were cultured with plate-bound Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 for 3 days. The resting Left Plot or activated Right Plot splenocytes were harvested, preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 , and then stained with either BD Horizon BV421 Rat IgG2b, kappa Isotype Control Cat. No. 562603; dashed line histograms or BD Horizon BV421 Rat Anti-Mouse CD279 PD-1 antibody Cat. No. 569780; solid line histograms at 0.5 mug/test. BD Via-Probe Cell Viability 7-AAD Solution Cat. No. 555815/555816 was added to cells right before analysis. The fluorescence histograms showing CD279 PD-1 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable 7-AAD-negative splenic leukocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Data shown on this Technical Data Sheet are not lot specific. Show More Flow cytometric analysis of CD279 PD-1 expression on resting and activated Mouse splenic leukocytes. C57BL/6 Mouse splenocytes were cultured with plate-bound Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 for 3 days. The resting Left Plot or activated Right Plot splenocytes were harvested, preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 , and then stained with either BD Horizon BV421 Rat IgG2b, kappa Isotype Control Cat. No. 562603; dashed line histograms or BD Horizon BV421 Rat Anti-Mouse CD279 PD-1 antibody Cat. No. 569780; solid line histograms at 0.5 mug/test. BD Via-Probe Cell Viability 7-AAD Solution Cat. No. 555815/555816 was added to cells right before analysis. The fluorescence histograms showing CD279 PD-1 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable 7-AAD-negative splenic leukocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Data shown on this Technical Data Sheet are not lot specific. Show More Flow cytometric analysis of CD279 PD-1 expression on resting and activated Mouse splenic leukocytes. C57BL/6 Mouse splenocytes were cultured with plate-bound Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 for 3 days. The resting Left Plot or activated Right Plot splenocytes were harvested, preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 , and then stained with either BD Horizon BV421 Rat IgG2b, kappa Isotype Control Cat. No. 562603; dashed line histograms or BD Horizon BV421 Rat Anti-Mouse CD279 PD-1 antibody Cat. No. 569780; solid line histograms at 0.5 mug/test. BD Via-Probe Cell Viability 7-AAD Solution Cat. No. 555815/555816 was added to cells right before analysis. The fluorescence histograms showing CD279 PD-1 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable 7-AAD-negative splenic leukocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Data shown on this Technical Data Sheet are not lot specific. Flow cytometric analysis of CD279 PD-1 expression on resting and activated Mouse splenic leukocytes. C57BL/6 Mouse splenocytes were cultured with plate-bound Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 for 3 days. The resting Left Plot or activated Right Plot splenocytes were harvested, preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 , and then stained with either BD Horizon BV421 Rat IgG2b, kappa Isotype Control Cat. No. 562603; dashed line histograms or BD Horizon BV421 Rat Anti-Mouse CD279 PD-1 antibody Cat. No. 569780; solid line histograms at 0.5 mug/test. BD Via-Probe Cell Viability 7-AAD Solution Cat. No. 555815/555816 was added to cells right before analysis. The fluorescence histograms showing CD279 PD-1 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable 7-AAD-negative splenic leukocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Data shown on this Technical Data Sheet are not lot specific.