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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, κ 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, κ 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, κ 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, κ 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, κ 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, κ 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.
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The 145-2C11 monoclonal antibody specifically binds to the 25-kDa ε chain of the T-cell receptor-associated CD3 complex that is expressed on thymocytes, mature T lymphocytes, and NK-T cells. The cytoplasmic domain of CD3e participates in the signal transduction events that activate several cellular biochemical pathways as a result of antigen recognition. Soluble 145-2C11 antibody can activate either unprimed (naive) or primed (memory/preactivated) T cells in vivo or in vitro, in the presence of Fc receptor-bearing accessory cells. In contrast, plate-bound 145-2C11 can activate T cells in the absence of accessory cells. Soluble 145-2C11 antibody has been reported to induce re-directed lysis of Fc receptor-bearing target cells by CTL clones and can also block lysis of specific target cells by antigen-specific CTL's. Under some conditions, T-cell activation by 145-2C11 antibody has been reported to result in apoptotic cell death. The 145-2C11 antibody does not cross-react with rat leukocytes. Preincubation of thymus cell suspensions at 37°C for 2-4 hours prior to staining reportedly enhances the ability of anti-CD3ε and anti-αβ TCR mAbs to detect the T-cell receptor on immature thymocytes.
The antibody was conjugated to BD Horizon™ BV421 which is part of the BD Horizon™ Brilliant Violet™ family of dyes. With an Ex Max of 407-nm and Em Max at 421-nm, BD Horizon™ BV421 can be excited by the violet laser and detected in the standard Pacific Blue™ filter set (eg, 450/50-nm filter). BD Horizon™ BV421 conjugates are very bright, often exhibiting a 10 fold improvement in brightness compared to Pacific Blue™ conjugates..
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