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Two-color flow cytometric analysis of B220/CD45R expressed on mouse splenocytes. Splenic leucocytes from a BALB/c mouse were stained with BD Horizon™ PE-CF594 Hamster Anti-Mouse CD3e antibody (Cat. No. 562286/562332) and either BD Horizon™ BV510 Rat IgG2a, κ Isotype Control (Cat. No. 562952; Left Panel) or BD Horizon™ BV510 Rat Anti-Mouse B220/CD45R antibody (Cat. No. 563103; Right Panel). Two-color flow cytometric dot plots show the correlated expression patterns of CD3 versus B220/CD45R (or Ig Isotype control staining) for gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.
Two-color flow cytometric analysis of B220/CD45R expressed on mouse splenocytes. Splenic leucocytes from a BALB/c mouse were stained with BD Horizon™ PE-CF594 Hamster Anti-Mouse CD3e antibody (Cat. No. 562286/562332) and either BD Horizon™ BV510 Rat IgG2a, κ Isotype Control (Cat. No. 562952; Left Panel) or BD Horizon™ BV510 Rat Anti-Mouse B220/CD45R antibody (Cat. No. 563103; Right Panel). Two-color flow cytometric dot plots show the correlated expression patterns of CD3 versus B220/CD45R (or Ig Isotype control staining) for gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.
Two-color flow cytometric analysis of B220/CD45R expressed on mouse splenocytes. Splenic leucocytes from a BALB/c mouse were stained with BD Horizon™ PE-CF594 Hamster Anti-Mouse CD3e antibody (Cat. No. 562286/562332) and either BD Horizon™ BV510 Rat IgG2a, κ Isotype Control (Cat. No. 562952; Left Panel) or BD Horizon™ BV510 Rat Anti-Mouse B220/CD45R antibody (Cat. No. 563103; Right Panel). Two-color flow cytometric dot plots show the correlated expression patterns of CD3 versus B220/CD45R (or Ig Isotype control staining) for gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.
Two-color flow cytometric analysis of B220/CD45R expressed on mouse splenocytes. Splenic leucocytes from a BALB/c mouse were stained with BD Horizon™ PE-CF594 Hamster Anti-Mouse CD3e antibody (Cat. No. 562286/562332) and either BD Horizon™ BV510 Rat IgG2a, κ Isotype Control (Cat. No. 562952; Left Panel) or BD Horizon™ BV510 Rat Anti-Mouse B220/CD45R antibody (Cat. No. 563103; Right Panel). Two-color flow cytometric dot plots show the correlated expression patterns of CD3 versus B220/CD45R (or Ig Isotype control staining) for gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.
Two-color flow cytometric analysis of B220/CD45R expressed on mouse splenocytes. Splenic leucocytes from a BALB/c mouse were stained with BD Horizon™ PE-CF594 Hamster Anti-Mouse CD3e antibody (Cat. No. 562286/562332) and either BD Horizon™ BV510 Rat IgG2a, κ Isotype Control (Cat. No. 562952; Left Panel) or BD Horizon™ BV510 Rat Anti-Mouse B220/CD45R antibody (Cat. No. 563103; Right Panel). Two-color flow cytometric dot plots show the correlated expression patterns of CD3 versus B220/CD45R (or Ig Isotype control staining) for gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.
Two-color flow cytometric analysis of B220/CD45R expressed on mouse splenocytes. Splenic leucocytes from a BALB/c mouse were stained with BD Horizon™ PE-CF594 Hamster Anti-Mouse CD3e antibody (Cat. No. 562286/562332) and either BD Horizon™ BV510 Rat IgG2a, κ Isotype Control (Cat. No. 562952; Left Panel) or BD Horizon™ BV510 Rat Anti-Mouse B220/CD45R antibody (Cat. No. 563103; Right Panel). Two-color flow cytometric dot plots show the correlated expression patterns of CD3 versus B220/CD45R (or Ig Isotype control staining) for gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.
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The RA3-6B2 monoclonal antibody specifically binds to an epitope on the extracellular domain of the transmembrane CD45 glycoprotein which is dependent upon the expression of exon A and specific carbohydrate residues. It is expressed on B lymphocytes at all stages from pro-B through mature and activated B cell, but it is decreased on plasma cells and a subset of memory B cells. The levels of CD45R expression on the B-cell lineage appear to be developmentally regulated. It is also reportedly found on the abnormal T cells involved in the lymphadenopathy of lpr/lpr and gld/gld mutant mice, on lytically active subsets of lymphokine-activated killer cells (NK cells and non-MHC-restricted CTL), on apoptotic T lymphocytes of mice injected with bacterial superantigen, on a population of NK-cell precursors in the bone marrow, and on B-lymphocyte, T-lymphocyte, and macrophage progenitors in fetal liver. The CD45R antigen has been reported not to be on hematopoietic stem cells, naive T lymphocytes, or MHC-restricted CTL. CD45 is a member of the Protein Tyrosine Phosphatase (PTP) family: Its intracellular (COOH-terminal) region contains two PTP catalytic domains, and the extracellular region is highly variable due to alternative splicing of exons 4, 5, and 6 (designated A, B, and C, respectively), plus differing levels of glycosylation. The CD45 isoforms detected in the mouse are cell type-, maturation, and activation state-specific. The CD45 isoforms play complex roles in T-cell and B-cell antigen receptor signal transduction. CD45R is commonly used as a pan B-cell marker; however, CD19 expression, detectable by the rat anti-mouse CD19 antibody (clone 1D3), is reported to be more restricted to the B-cell lineage. The rat anti-mouse CD45R antibody (clone RA3-6B2) has been reported to enhance isotype switching during in vitro B-cell responses and to inhibit in vivo B-cell responses. Cross-reaction of the RA3-6B2 clone with activated human T lymphocytes has also been reportedly observed.
The antibody was conjugated to BD Horizon™ BV510 which is part of the BD Horizon™ Brilliant Violet™ family of dyes. With an Ex Max of 405-nm and Em Max at 510-nm, BD Horizon™ BV510 can be excited by the violet laser and detected in the BD Horizon™ V500 (525/50-nm) filter set. BD Horizon™ BV510 conjugates are useful for the detection of dim markers off the violet laser.
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