BD PharmingenTM APC Rat Anti-Mouse CD223

Description

Multicolor flow cytometric analysis of CD223 expressed on activated splenocytes. Splenocytes from C57BL/6 mice were activated in culture for 3 days in the presence of immobilized Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 . The cells were then harvested and stained with PE Hamster Anti-Mouse CD3e antibody Cat. No. 553063/553064/561824 and either APC Rat IgG1, kappa Isotype Control Cat. No. 554686, Left Panel or APC Rat Anti-Mouse CD223 antibody Cat. No. 562346, Right Panel . Two-color flow cytometric dot plots showing the correlated expression patterns of CD3 versus CD223 or Ig Isotype Control staining were derived from gated events with the forward and side light-scatter characteristics of viable activated splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD223 expressed on activated splenocytes. Splenocytes from C57BL/6 mice were activated in culture for 3 days in the presence of immobilized Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 . The cells were then harvested and stained with PE Hamster Anti-Mouse CD3e antibody Cat. No. 553063/553064/561824 and either APC Rat IgG1, kappa Isotype Control Cat. No. 554686, Left Panel or APC Rat Anti-Mouse CD223 antibody Cat. No. 562346, Right Panel . Two-color flow cytometric dot plots showing the correlated expression patterns of CD3 versus CD223 or Ig Isotype Control staining were derived from gated events with the forward and side light-scatter characteristics of viable activated splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD223 expressed on activated splenocytes. Splenocytes from C57BL/6 mice were activated in culture for 3 days in the presence of immobilized Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 . The cells were then harvested and stained with PE Hamster Anti-Mouse CD3e antibody Cat. No. 553063/553064/561824 and either APC Rat IgG1, kappa Isotype Control Cat. No. 554686, Left Panel or APC Rat Anti-Mouse CD223 antibody Cat. No. 562346, Right Panel . Two-color flow cytometric dot plots showing the correlated expression patterns of CD3 versus CD223 or Ig Isotype Control staining were derived from gated events with the forward and side light-scatter characteristics of viable activated splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Multicolor flow cytometric analysis of CD223 expressed on activated splenocytes. Splenocytes from C57BL/6 mice were activated in culture for 3 days in the presence of immobilized Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 . The cells were then harvested and stained with PE Hamster Anti-Mouse CD3e antibody Cat. No. 553063/553064/561824 and either APC Rat IgG1, kappa Isotype Control Cat. No. 554686, Left Panel or APC Rat Anti-Mouse CD223 antibody Cat. No. 562346, Right Panel . Two-color flow cytometric dot plots showing the correlated expression patterns of CD3 versus CD223 or Ig Isotype Control staining were derived from gated events with the forward and side light-scatter characteristics of viable activated splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Multicolor flow cytometric analysis of CD223 expressed on activated splenocytes. Splenocytes from C57BL/6 mice were activated in culture for 3 days in the presence of immobilized Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 . The cells were then harvested and stained with PE Hamster Anti-Mouse CD3e antibody Cat. No. 553063/553064/561824 and either APC Rat IgG1, kappa Isotype Control Cat. No. 554686, Left Panel or APC Rat Anti-Mouse CD223 antibody Cat. No. 562346, Right Panel . Two-color flow cytometric dot plots showing the correlated expression patterns of CD3 versus CD223 or Ig Isotype Control staining were derived from gated events with the forward and side light-scatter characteristics of viable activated splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD223 expressed on activated splenocytes. Splenocytes from C57BL/6 mice were activated in culture for 3 days in the presence of immobilized Purified NA/LE Hamster Anti-Mouse CD3e antibody Cat. No. 553057 . The cells were then harvested and stained with PE Hamster Anti-Mouse CD3e antibody Cat. No. 553063/553064/561824 and either APC Rat IgG1, kappa Isotype Control Cat. No. 554686, Left Panel or APC Rat Anti-Mouse CD223 antibody Cat. No. 562346, Right Panel . Two-color flow cytometric dot plots showing the correlated expression patterns of CD3 versus CD223 or Ig Isotype Control staining were derived from gated events with the forward and side light-scatter characteristics of viable activated splenocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System.