BD HorizonTM BV510 Mouse Anti-Mouse NK-1.1

Description

Two-color flow cytometric analysis of NK-1.1 expression on mouse splenocytes. Splenic leucocytes from a C57BL/6 mouse were stained with PE Hamster Anti-Mouse CD3e antibody Cat. No. 553064/553063/561824 and either BD Horizon BV510 Mouse IgG2a, kappa Isotype Control Cat. No. 563027, Left Panel or BD Horizon BV510 Mouse Anti-Mouse NK-1.1 Cat. No. 563096; Right Panel . Two-color flow cytometric dot plots show the correlated expression patterns of NK1.1 or Ig Isotype control staining versus CD3e for gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Two-color flow cytometric analysis of NK-1.1 expression on mouse splenocytes. Splenic leucocytes from a C57BL/6 mouse were stained with PE Hamster Anti-Mouse CD3e antibody Cat. No. 553064/553063/561824 and either BD Horizon BV510 Mouse IgG2a, kappa Isotype Control Cat. No. 563027, Left Panel or BD Horizon BV510 Mouse Anti-Mouse NK-1.1 Cat. No. 563096; Right Panel . Two-color flow cytometric dot plots show the correlated expression patterns of NK1.1 or Ig Isotype control staining versus CD3e for gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Two-color flow cytometric analysis of NK-1.1 expression on mouse splenocytes. Splenic leucocytes from a C57BL/6 mouse were stained with PE Hamster Anti-Mouse CD3e antibody Cat. No. 553064/553063/561824 and either BD Horizon BV510 Mouse IgG2a, kappa Isotype Control Cat. No. 563027, Left Panel or BD Horizon BV510 Mouse Anti-Mouse NK-1.1 Cat. No. 563096; Right Panel . Two-color flow cytometric dot plots show the correlated expression patterns of NK1.1 or Ig Isotype control staining versus CD3e for gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Two-color flow cytometric analysis of NK-1.1 expression on mouse splenocytes. Splenic leucocytes from a C57BL/6 mouse were stained with PE Hamster Anti-Mouse CD3e antibody Cat. No. 553064/553063/561824 and either BD Horizon BV510 Mouse IgG2a, kappa Isotype Control Cat. No. 563027, Left Panel or BD Horizon BV510 Mouse Anti-Mouse NK-1.1 Cat. No. 563096; Right Panel . Two-color flow cytometric dot plots show the correlated expression patterns of NK1.1 or Ig Isotype control staining versus CD3e for gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Two-color flow cytometric analysis of NK-1.1 expression on mouse splenocytes. Splenic leucocytes from a C57BL/6 mouse were stained with PE Hamster Anti-Mouse CD3e antibody Cat. No. 553064/553063/561824 and either BD Horizon BV510 Mouse IgG2a, kappa Isotype Control Cat. No. 563027, Left Panel or BD Horizon BV510 Mouse Anti-Mouse NK-1.1 Cat. No. 563096; Right Panel . Two-color flow cytometric dot plots show the correlated expression patterns of NK1.1 or Ig Isotype control staining versus CD3e for gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Two-color flow cytometric analysis of NK-1.1 expression on mouse splenocytes. Splenic leucocytes from a C57BL/6 mouse were stained with PE Hamster Anti-Mouse CD3e antibody Cat. No. 553064/553063/561824 and either BD Horizon BV510 Mouse IgG2a, kappa Isotype Control Cat. No. 563027, Left Panel or BD Horizon BV510 Mouse Anti-Mouse NK-1.1 Cat. No. 563096; Right Panel . Two-color flow cytometric dot plots show the correlated expression patterns of NK1.1 or Ig Isotype control staining versus CD3e for gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System.