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- BD Horizon RealViolet™ 828 for Flow Cytometry
- Quality and Reproducibility
- Single Color Antibodies RUO
- Panels Multicolor Cocktails RUO
- Flow Cytometry Controls and Lysates
- buffers and Supporting Reagents RUO
- Cell Function Analysis Stains Dyes
- Single Color Antibodies
- Compensation Beads
- BD Horizon™ Human T Cell Backbone Panel
- BD Pharmingen™ MonoBlock™ Leukocyte Staining Buffer
- BV605 Transition
- BD Horizon RealBlue™ 670 for Flow Cytometry
- BD Horizon RealBlue™ 780 for Flow Cytometry
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- BD Horizon RealYellow™ 610
- BD Horizon RealYellow™ 703
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BD Pharmingen™ PE Rat Anti-Mouse CD268 (BAFF-R)
Clone 7H22-E16 (RUO)
Multicolor flow cytometric analysis of mouse CD268 (BAFF-R) expression.
Left Panel - Spleen. BALB/c splenic leucocytes were stained with APC Rat Anti-Mouse CD45R/B220 antibody (Cat. No. 553092/561880), and either PE Rat IgG1, κ Isotype Control (Cat. No. 554685; Left Plot), or PE Rat Anti-Mouse CD268 (BAFF-R) antibody (Cat. No. 565783; Right Plot). Two-color flow cytometric contour plots showing the correlated expression of CD268 (BAFF-R) [or Ig Isotype control staining] versus CD45R/B220 were derived from gated events with the forward and side light-scatter characteristics of viable leucocytes.
Right Panel: Bone Marrow. BALB/c bone marrow cells were stained with APC Rat Anti-Mouse CD45R/B220 and BD Horizon™ BUV395 Rat Anti-Mouse IgM (Cat. No. 564025) antibodies, and either PE Rat IgG1, κ Isotype Control (Left Plot) or PE Rat Anti-Mouse CD268 (BAFF-R) antibody (Right Plot). Two-color flow cytometric contour plots showing the correlated expression of CD268 (BAFF-R) [or Ig Isotype control staining] versus IgM were derived from CD45R/B220-positive gated events with the forward and side light-scatter characteristics of viable bone marrow cells.
Flow cytometric analysis was performed using a BD LSRFortessa™ X-20 Cell Analyzer System.
Multicolor flow cytometric analysis of mouse CD268 (BAFF-R) expression.
Left Panel - Spleen. BALB/c splenic leucocytes were stained with APC Rat Anti-Mouse CD45R/B220 antibody (Cat. No. 553092/561880), and either PE Rat IgG1, κ Isotype Control (Cat. No. 554685; Left Plot), or PE Rat Anti-Mouse CD268 (BAFF-R) antibody (Cat. No. 565783; Right Plot). Two-color flow cytometric contour plots showing the correlated expression of CD268 (BAFF-R) [or Ig Isotype control staining] versus CD45R/B220 were derived from gated events with the forward and side light-scatter characteristics of viable leucocytes.
Right Panel: Bone Marrow. BALB/c bone marrow cells were stained with APC Rat Anti-Mouse CD45R/B220 and BD Horizon™ BUV395 Rat Anti-Mouse IgM (Cat. No. 564025) antibodies, and either PE Rat IgG1, κ Isotype Control (Left Plot) or PE Rat Anti-Mouse CD268 (BAFF-R) antibody (Right Plot). Two-color flow cytometric contour plots showing the correlated expression of CD268 (BAFF-R) [or Ig Isotype control staining] versus IgM were derived from CD45R/B220-positive gated events with the forward and side light-scatter characteristics of viable bone marrow cells.
Flow cytometric analysis was performed using a BD LSRFortessa™ X-20 Cell Analyzer System.
Multicolor flow cytometric analysis of mouse CD268 (BAFF-R) expression.
Left Panel - Spleen. BALB/c splenic leucocytes were stained with APC Rat Anti-Mouse CD45R/B220 antibody (Cat. No. 553092/561880), and either PE Rat IgG1, κ Isotype Control (Cat. No. 554685; Left Plot), or PE Rat Anti-Mouse CD268 (BAFF-R) antibody (Cat. No. 565783; Right Plot). Two-color flow cytometric contour plots showing the correlated expression of CD268 (BAFF-R) [or Ig Isotype control staining] versus CD45R/B220 were derived from gated events with the forward and side light-scatter characteristics of viable leucocytes.
Right Panel: Bone Marrow. BALB/c bone marrow cells were stained with APC Rat Anti-Mouse CD45R/B220 and BD Horizon™ BUV395 Rat Anti-Mouse IgM (Cat. No. 564025) antibodies, and either PE Rat IgG1, κ Isotype Control (Left Plot) or PE Rat Anti-Mouse CD268 (BAFF-R) antibody (Right Plot). Two-color flow cytometric contour plots showing the correlated expression of CD268 (BAFF-R) [or Ig Isotype control staining] versus IgM were derived from CD45R/B220-positive gated events with the forward and side light-scatter characteristics of viable bone marrow cells.
Flow cytometric analysis was performed using a BD LSRFortessa™ X-20 Cell Analyzer System.
Regulatory Status Legend
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
Preparation And Storage
Product Notices
- Since applications vary, each investigator should titrate the reagent to obtain optimal results.
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
- Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
- For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
- An isotype control should be used at the same concentration as the antibody of interest.
Companion Products
The 7H22-E16 monoclonal antibody specifically binds to CD268, which is also known as, B cell-activating factor receptor (BAFF-R), or BAFF Receptor 3 (BR3). CD268 is a type III transmembrane protein that is likewise known as Tumor necrosis factor receptor superfamily member 13C (Tnfrsf13c). CD268/BAFF-R is a receptor for CD257 (also known as, BAFF, Blys, TALL-1, or THANK) and is expressed on B cells and a subset of activated/memory CD4+ T cells. B cells express two other BAFF receptors, CD267/TACI, or CD269/BCMA, at various times during their differentiation. CD268/BAFF-R expression starts at the transitional stage of B cell development and increases throughout B cell maturation. CD267/BAFF-R mediates most BAFF-dependent functions including B cell survival, the activation of B cell proliferation and immunoglobulin secretion, and the costimulation of T cells. Overexpression of BAFF in mice and humans is associated with autoimmunity, whereas CD268/BAFF-R deficiency may cause severe impairment in humoral responses.
Development References (3)
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Giltiay NV, Lu Y, Allman D, Jørgensen TN, Li X. The adaptor molecule Act1 regulates BAFF responsiveness and self-reactive B cell selection during transitional B cell maturation.. J Immunol. 2010; 185(1):99-109. (Clone-specific: Flow cytometry). View Reference
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Naradikian MS, Perate AR, Cancro MP. BAFF receptors and ligands create independent homeostatic niches for B cell subsets.. Curr Opin Immunol. 2015; 34:126-129. (Biology). View Reference
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Ng LG, Sutherland AP, Newton R, et al. B cell-activating factor belonging to the TNF family (BAFF)-R is the principal BAFF receptor facilitating BAFF costimulation of circulating T and B cells.. J Immunol. 2004; 173(2):807-17. (Immunogen: Flow cytometry). View Reference
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Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
For Research Use Only. Not for use in diagnostic or therapeutic procedures.