
563157 ·
BDB Bioscience · Cat: 563157
Reach 3+ verified distributors
Manufacturer product page
bdbiosciences.com/en-us/products/reagents/flow-cytometry-rea...Description
Multicolor flow cytometric analysis of CD19 expression on mouse splenocytes. Splenic leucocytes from a BALB/c mouse were stained simultaneously with APC Hamster Anti-Mouse CD3e antibody Cat. No. 553066/561826 and either BD Horizon BV711 Rat IgG2a, kappa Isotype Control Cat. No. 563047; Left Panel or BD Horizon BV711 Rat Anti-Mouse CD19 Cat. No. 563157; Right Panel . Two-color flow cytometric dot plots showing the expression of CD19 or Ig Isotype control staining versus CD3 were derived from gated events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD19 expression on mouse splenocytes. Splenic leucocytes from a BALB/c mouse were stained simultaneously with APC Hamster Anti-Mouse CD3e antibody Cat. No. 553066/561826 and either BD Horizon BV711 Rat IgG2a, kappa Isotype Control Cat. No. 563047; Left Panel or BD Horizon BV711 Rat Anti-Mouse CD19 Cat. No. 563157; Right Panel . Two-color flow cytometric dot plots showing the expression of CD19 or Ig Isotype control staining versus CD3 were derived from gated events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD19 expression on mouse splenocytes. Splenic leucocytes from a BALB/c mouse were stained simultaneously with APC Hamster Anti-Mouse CD3e antibody Cat. No. 553066/561826 and either BD Horizon BV711 Rat IgG2a, kappa Isotype Control Cat. No. 563047; Left Panel or BD Horizon BV711 Rat Anti-Mouse CD19 Cat. No. 563157; Right Panel . Two-color flow cytometric dot plots showing the expression of CD19 or Ig Isotype control staining versus CD3 were derived from gated 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 Multicolor flow cytometric analysis of CD19 expression on mouse splenocytes. Splenic leucocytes from a BALB/c mouse were stained simultaneously with APC Hamster Anti-Mouse CD3e antibody Cat. No. 553066/561826 and either BD Horizon BV711 Rat IgG2a, kappa Isotype Control Cat. No. 563047; Left Panel or BD Horizon BV711 Rat Anti-Mouse CD19 Cat. No. 563157; Right Panel . Two-color flow cytometric dot plots showing the expression of CD19 or Ig Isotype control staining versus CD3 were derived from gated 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 Multicolor flow cytometric analysis of CD19 expression on mouse splenocytes. Splenic leucocytes from a BALB/c mouse were stained simultaneously with APC Hamster Anti-Mouse CD3e antibody Cat. No. 553066/561826 and either BD Horizon BV711 Rat IgG2a, kappa Isotype Control Cat. No. 563047; Left Panel or BD Horizon BV711 Rat Anti-Mouse CD19 Cat. No. 563157; Right Panel . Two-color flow cytometric dot plots showing the expression of CD19 or Ig Isotype control staining versus CD3 were derived from gated events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD19 expression on mouse splenocytes. Splenic leucocytes from a BALB/c mouse were stained simultaneously with APC Hamster Anti-Mouse CD3e antibody Cat. No. 553066/561826 and either BD Horizon BV711 Rat IgG2a, kappa Isotype Control Cat. No. 563047; Left Panel or BD Horizon BV711 Rat Anti-Mouse CD19 Cat. No. 563157; Right Panel . Two-color flow cytometric dot plots showing the expression of CD19 or Ig Isotype control staining versus CD3 were derived from gated events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System.







