BD PharmingenTM Alexa Fluor 647 Rat Anti-Human CD294

Description

Flow cytometric analysis of CD294 expression on human peripheral blood cells. Whole blood was stained with PE mouse anti-human CD45 Cat. No. 555483/560975 and either Alexa Fluor 647Rat Anti-Human CD294 antibody Cat. No. 558042/561797; right panel or with an Alexa Fluor 647 Rat IgG2a, kappa Isotype Control Cat. No. 557690; left panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of whole blood cells. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD294 expression on human peripheral blood cells. Whole blood was stained with PE mouse anti-human CD45 Cat. No. 555483/560975 and either Alexa Fluor 647Rat Anti-Human CD294 antibody Cat. No. 558042/561797; right panel or with an Alexa Fluor 647 Rat IgG2a, kappa Isotype Control Cat. No. 557690; left panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of whole blood cells. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD294 expression on human peripheral blood cells. Whole blood was stained with PE mouse anti-human CD45 Cat. No. 555483/560975 and either Alexa Fluor 647Rat Anti-Human CD294 antibody Cat. No. 558042/561797; right panel or with an Alexa Fluor 647 Rat IgG2a, kappa Isotype Control Cat. No. 557690; left panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of whole blood cells. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD294 expression on human peripheral blood cells. Whole blood was stained with PE mouse anti-human CD45 Cat. No. 555483/560975 and either Alexa Fluor 647Rat Anti-Human CD294 antibody Cat. No. 558042/561797; right panel or with an Alexa Fluor 647 Rat IgG2a, kappa Isotype Control Cat. No. 557690; left panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of whole blood cells. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD294 expression on human peripheral blood cells. Whole blood was stained with PE mouse anti-human CD45 Cat. No. 555483/560975 and either Alexa Fluor 647Rat Anti-Human CD294 antibody Cat. No. 558042/561797; right panel or with an Alexa Fluor 647 Rat IgG2a, kappa Isotype Control Cat. No. 557690; left panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of whole blood cells. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD294 expression on human peripheral blood cells. Whole blood was stained with PE mouse anti-human CD45 Cat. No. 555483/560975 and either Alexa Fluor 647Rat Anti-Human CD294 antibody Cat. No. 558042/561797; right panel or with an Alexa Fluor 647 Rat IgG2a, kappa Isotype Control Cat. No. 557690; left panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of whole blood cells. Flow cytometry was performed using a BD LSR II Flow Cytometer System.