
561828 · 25 ug
BDB Bioscience · Cat: 561828
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bdbiosciences.com/en-us/products/reagents/flow-cytometry-rea...Description
Multicolor flow cytometric analysis of CD4 expression on mouse splenocytes. Splenic leukocytes were stained simultaneously with PE Hamster Anti-Mouse CD3e antibody Cat. No. 561824/553063/553064 and with either BD Pharmingen FITC Rat IgG2a, kappa Isotype Control Cat. No. 553988; Left Panel or BD Pharmingen FITC Rat Anti-Mouse CD4 antibody Cat. No. 553729; Right Panel . Two-color flow cytometric dot plots show the correlated expression patterns of CD4 or Ig Isotype control staining versus CD3 for gated events with the forward and side light-scatter characteristics of viable splenic leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD4 expression on mouse splenocytes. Splenic leukocytes were stained simultaneously with PE Hamster Anti-Mouse CD3e antibody Cat. No. 561824/553063/553064 and with either BD Pharmingen FITC Rat IgG2a, kappa Isotype Control Cat. No. 553988; Left Panel or BD Pharmingen FITC Rat Anti-Mouse CD4 antibody Cat. No. 553729; Right Panel . Two-color flow cytometric dot plots show the correlated expression patterns of CD4 or Ig Isotype control staining versus CD3 for gated events with the forward and side light-scatter characteristics of viable splenic leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD4 expression on mouse splenocytes. Splenic leukocytes were stained simultaneously with PE Hamster Anti-Mouse CD3e antibody Cat. No. 561824/553063/553064 and with either BD Pharmingen FITC Rat IgG2a, kappa Isotype Control Cat. No. 553988; Left Panel or BD Pharmingen FITC Rat Anti-Mouse CD4 antibody Cat. No. 553729; Right Panel . Two-color flow cytometric dot plots show the correlated expression patterns of CD4 or Ig Isotype control staining versus CD3 for gated events with the forward and side light-scatter characteristics of viable splenic leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Multicolor flow cytometric analysis of CD4 expression on mouse splenocytes. Splenic leukocytes were stained simultaneously with PE Hamster Anti-Mouse CD3e antibody Cat. No. 561824/553063/553064 and with either BD Pharmingen FITC Rat IgG2a, kappa Isotype Control Cat. No. 553988; Left Panel or BD Pharmingen FITC Rat Anti-Mouse CD4 antibody Cat. No. 553729; Right Panel . Two-color flow cytometric dot plots show the correlated expression patterns of CD4 or Ig Isotype control staining versus CD3 for gated events with the forward and side light-scatter characteristics of viable splenic leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Multicolor flow cytometric analysis of CD4 expression on mouse splenocytes. Splenic leukocytes were stained simultaneously with PE Hamster Anti-Mouse CD3e antibody Cat. No. 561824/553063/553064 and with either BD Pharmingen FITC Rat IgG2a, kappa Isotype Control Cat. No. 553988; Left Panel or BD Pharmingen FITC Rat Anti-Mouse CD4 antibody Cat. No. 553729; Right Panel . Two-color flow cytometric dot plots show the correlated expression patterns of CD4 or Ig Isotype control staining versus CD3 for gated events with the forward and side light-scatter characteristics of viable splenic leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD4 expression on mouse splenocytes. Splenic leukocytes were stained simultaneously with PE Hamster Anti-Mouse CD3e antibody Cat. No. 561824/553063/553064 and with either BD Pharmingen FITC Rat IgG2a, kappa Isotype Control Cat. No. 553988; Left Panel or BD Pharmingen FITC Rat Anti-Mouse CD4 antibody Cat. No. 553729; Right Panel . Two-color flow cytometric dot plots show the correlated expression patterns of CD4 or Ig Isotype control staining versus CD3 for gated events with the forward and side light-scatter characteristics of viable splenic leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System.