BD PharmingenTM PE Mouse anti-Human CD160

Description

Flow cytometric analysis CD160 expression on human peripheral blood lymphocytes. Human whole blood cells were stained with APC Mouse Anti-Human CD56 Cat. No. 555518 and either PE Mouse IgM, kappa Isotype Control Cat. No. 555584; Left Panel or PE Mouse anti-Human CD160 Cat. No. 562118; Right Panel . After incubation the erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-color dot plots showing the correlated expression of CD160 or background Ig isotype control staining versus CD56 were derived from gated events of the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD FACSCanto II Flow Cytometer System. Flow cytometric analysis CD160 expression on human peripheral blood lymphocytes. Human whole blood cells were stained with APC Mouse Anti-Human CD56 Cat. No. 555518 and either PE Mouse IgM, kappa Isotype Control Cat. No. 555584; Left Panel or PE Mouse anti-Human CD160 Cat. No. 562118; Right Panel . After incubation the erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-color dot plots showing the correlated expression of CD160 or background Ig isotype control staining versus CD56 were derived from gated events of the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD FACSCanto II Flow Cytometer System. Flow cytometric analysis CD160 expression on human peripheral blood lymphocytes. Human whole blood cells were stained with APC Mouse Anti-Human CD56 Cat. No. 555518 and either PE Mouse IgM, kappa Isotype Control Cat. No. 555584; Left Panel or PE Mouse anti-Human CD160 Cat. No. 562118; Right Panel . After incubation the erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-color dot plots showing the correlated expression of CD160 or background Ig isotype control staining versus CD56 were derived from gated events of the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD FACSCanto II Flow Cytometer System. Show More Flow cytometric analysis CD160 expression on human peripheral blood lymphocytes. Human whole blood cells were stained with APC Mouse Anti-Human CD56 Cat. No. 555518 and either PE Mouse IgM, kappa Isotype Control Cat. No. 555584; Left Panel or PE Mouse anti-Human CD160 Cat. No. 562118; Right Panel . After incubation the erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-color dot plots showing the correlated expression of CD160 or background Ig isotype control staining versus CD56 were derived from gated events of the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD FACSCanto II Flow Cytometer System. Show More Flow cytometric analysis CD160 expression on human peripheral blood lymphocytes. Human whole blood cells were stained with APC Mouse Anti-Human CD56 Cat. No. 555518 and either PE Mouse IgM, kappa Isotype Control Cat. No. 555584; Left Panel or PE Mouse anti-Human CD160 Cat. No. 562118; Right Panel . After incubation the erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-color dot plots showing the correlated expression of CD160 or background Ig isotype control staining versus CD56 were derived from gated events of the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD FACSCanto II Flow Cytometer System. Flow cytometric analysis CD160 expression on human peripheral blood lymphocytes. Human whole blood cells were stained with APC Mouse Anti-Human CD56 Cat. No. 555518 and either PE Mouse IgM, kappa Isotype Control Cat. No. 555584; Left Panel or PE Mouse anti-Human CD160 Cat. No. 562118; Right Panel . After incubation the erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-color dot plots showing the correlated expression of CD160 or background Ig isotype control staining versus CD56 were derived from gated events of the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD FACSCanto II Flow Cytometer System.