
562600 ·
BDB Bioscience · Cat: 562600
Reach 3+ verified distributors
Manufacturer product page
bdbiosciences.com/en-us/products/reagents/flow-cytometry-rea...Description
Two-color flow cytometric analysis of CD3e expressed on mouse splenocytes. BALB/c splenocytes were stained with APC Rat Anti-Mouse CD4 Cat. No. 553051 and APC Rat Anti-Mouse CD8a Cat. No. 561093/553035 and either BD Horizon BV421 Armenian Hamster IgG1, kappa Isotype Control Cat. No. 562601; Left Panel or BD Horizon BV421 Hamster Anti-Mouse CD3e antibody Cat. No. 562600; Right Panel . The two-color flow cytometric dot plots showing CD3 or Ig Isotype Control staining versus CD4 and CD8 were derived from events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD FACSCanto II Flow Cytometer System. Two-color flow cytometric analysis of CD3e expressed on mouse splenocytes. BALB/c splenocytes were stained with APC Rat Anti-Mouse CD4 Cat. No. 553051 and APC Rat Anti-Mouse CD8a Cat. No. 561093/553035 and either BD Horizon BV421 Armenian Hamster IgG1, kappa Isotype Control Cat. No. 562601; Left Panel or BD Horizon BV421 Hamster Anti-Mouse CD3e antibody Cat. No. 562600; Right Panel . The two-color flow cytometric dot plots showing CD3 or Ig Isotype Control staining versus CD4 and CD8 were derived from events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD FACSCanto II Flow Cytometer System. Two-color flow cytometric analysis of CD3e expressed on mouse splenocytes. BALB/c splenocytes were stained with APC Rat Anti-Mouse CD4 Cat. No. 553051 and APC Rat Anti-Mouse CD8a Cat. No. 561093/553035 and either BD Horizon BV421 Armenian Hamster IgG1, kappa Isotype Control Cat. No. 562601; Left Panel or BD Horizon BV421 Hamster Anti-Mouse CD3e antibody Cat. No. 562600; Right Panel . The two-color flow cytometric dot plots showing CD3 or Ig Isotype Control staining versus CD4 and CD8 were derived from events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD FACSCanto II Flow Cytometer System. Show More Two-color flow cytometric analysis of CD3e expressed on mouse splenocytes. BALB/c splenocytes were stained with APC Rat Anti-Mouse CD4 Cat. No. 553051 and APC Rat Anti-Mouse CD8a Cat. No. 561093/553035 and either BD Horizon BV421 Armenian Hamster IgG1, kappa Isotype Control Cat. No. 562601; Left Panel or BD Horizon BV421 Hamster Anti-Mouse CD3e antibody Cat. No. 562600; Right Panel . The two-color flow cytometric dot plots showing CD3 or Ig Isotype Control staining versus CD4 and CD8 were derived from events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD FACSCanto II Flow Cytometer System. Show More Two-color flow cytometric analysis of CD3e expressed on mouse splenocytes. BALB/c splenocytes were stained with APC Rat Anti-Mouse CD4 Cat. No. 553051 and APC Rat Anti-Mouse CD8a Cat. No. 561093/553035 and either BD Horizon BV421 Armenian Hamster IgG1, kappa Isotype Control Cat. No. 562601; Left Panel or BD Horizon BV421 Hamster Anti-Mouse CD3e antibody Cat. No. 562600; Right Panel . The two-color flow cytometric dot plots showing CD3 or Ig Isotype Control staining versus CD4 and CD8 were derived from events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD FACSCanto II Flow Cytometer System. Two-color flow cytometric analysis of CD3e expressed on mouse splenocytes. BALB/c splenocytes were stained with APC Rat Anti-Mouse CD4 Cat. No. 553051 and APC Rat Anti-Mouse CD8a Cat. No. 561093/553035 and either BD Horizon BV421 Armenian Hamster IgG1, kappa Isotype Control Cat. No. 562601; Left Panel or BD Horizon BV421 Hamster Anti-Mouse CD3e antibody Cat. No. 562600; Right Panel . The two-color flow cytometric dot plots showing CD3 or Ig Isotype Control staining versus CD4 and CD8 were derived from events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometry was performed using a BD FACSCanto II Flow Cytometer System.