BD HorizonTM BV421 Rat Anti-Mouse CD24

Description

Multicolor flow cytometric analysis of CD24 expression on mouse splenocytes. Splenocytes from C57BL/6 mice were stained with Alexa Fluor 647 Rat Anti-Mouse CD3e antibody Cat. No. 557869 and with either a BD Horizon BV421 Rat IgG2b, kappa Isotype Control Cat. No. 562603, Left Panel or with the BD Horizon BV421 Rat Anti-Mouse CD24 antibody Cat. No. 562563, Right Panel . Two-color flow cytometric dot plots showing the correlated expression patterns of CD3 versus CD24 or Ig isotype control staining 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 CD24 expression on mouse splenocytes. Splenocytes from C57BL/6 mice were stained with Alexa Fluor 647 Rat Anti-Mouse CD3e antibody Cat. No. 557869 and with either a BD Horizon BV421 Rat IgG2b, kappa Isotype Control Cat. No. 562603, Left Panel or with the BD Horizon BV421 Rat Anti-Mouse CD24 antibody Cat. No. 562563, Right Panel . Two-color flow cytometric dot plots showing the correlated expression patterns of CD3 versus CD24 or Ig isotype control staining 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 CD24 expression on mouse splenocytes. Splenocytes from C57BL/6 mice were stained with Alexa Fluor 647 Rat Anti-Mouse CD3e antibody Cat. No. 557869 and with either a BD Horizon BV421 Rat IgG2b, kappa Isotype Control Cat. No. 562603, Left Panel or with the BD Horizon BV421 Rat Anti-Mouse CD24 antibody Cat. No. 562563, Right Panel . Two-color flow cytometric dot plots showing the correlated expression patterns of CD3 versus CD24 or Ig isotype control staining 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 CD24 expression on mouse splenocytes. Splenocytes from C57BL/6 mice were stained with Alexa Fluor 647 Rat Anti-Mouse CD3e antibody Cat. No. 557869 and with either a BD Horizon BV421 Rat IgG2b, kappa Isotype Control Cat. No. 562603, Left Panel or with the BD Horizon BV421 Rat Anti-Mouse CD24 antibody Cat. No. 562563, Right Panel . Two-color flow cytometric dot plots showing the correlated expression patterns of CD3 versus CD24 or Ig isotype control staining 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 CD24 expression on mouse splenocytes. Splenocytes from C57BL/6 mice were stained with Alexa Fluor 647 Rat Anti-Mouse CD3e antibody Cat. No. 557869 and with either a BD Horizon BV421 Rat IgG2b, kappa Isotype Control Cat. No. 562603, Left Panel or with the BD Horizon BV421 Rat Anti-Mouse CD24 antibody Cat. No. 562563, Right Panel . Two-color flow cytometric dot plots showing the correlated expression patterns of CD3 versus CD24 or Ig isotype control staining 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 CD24 expression on mouse splenocytes. Splenocytes from C57BL/6 mice were stained with Alexa Fluor 647 Rat Anti-Mouse CD3e antibody Cat. No. 557869 and with either a BD Horizon BV421 Rat IgG2b, kappa Isotype Control Cat. No. 562603, Left Panel or with the BD Horizon BV421 Rat Anti-Mouse CD24 antibody Cat. No. 562563, Right Panel . Two-color flow cytometric dot plots showing the correlated expression patterns of CD3 versus CD24 or Ig isotype control staining 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.