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Multiparameter flow cytometric analysis of CD209b expression on BALB/c versus C57BL/6 mouse peritoneal exudate cells (PECs). Resident peritoneal cells were harvested from BALB/c (Top Plots) or C57BL/6 (Bottom Plots) mice, washed, and then stained with BD Pharmingen™ Alexa Fluor™ 647 Rat Anti-CD11b antibody (Cat. No. 557686) and with either PE Rat IgM Isotype Control (Cat. No. 553943; Left Plots) or PE Rat Anti-Mouse CD209b antibody (Cat. No. 568710/568711; Right Plots) at 0.25 µg/test. The bivariate pseudocolor density plots showing the correlated expression of CD209b (or Ig Isotype control staining) versus CD11b were derived from gated events with the forward and side-light scatter characteristics of viable peritoneal cell populations. Flow cytometry and data analysis were performed using a BD LSRFortessa™ Cell Analyzer System and FlowJo™ software. Data shown on this Technical Data Sheet are not lot specific.
BD Pharmingen™ PE Rat Anti-Mouse CD209b (SIGN-R1)
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
Recommended Assay Procedures
BD® CompBeads can be used as surrogates to assess fluorescence spillover (compensation). When fluorochrome conjugated antibodies are bound to BD® CompBeads, they have spectral properties very similar to cells. However, for some fluorochromes there can be small differences in spectral emissions compared to cells, resulting in spillover values that differ when compared to biological controls. It is strongly recommended that when using a reagent for the first time, users compare the spillover on cell and BD® CompBeads to ensure that BD® CompBeads are appropriate for your specific cellular application.
Product Notices
- 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.
- Since applications vary, each investigator should titrate the reagent to obtain optimal results.
- 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.
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Companion Products
The ER-TR9 monoclonal antibody specifically recognizes mouse CD209 antigen-like protein B (CD209b) which is also known as Mouse SIGN-related 1 (mSIGNR1 or SIGNR1). CD209b is a mouse homolog of human CD209 (DC-SIGN) and is also referred to as DC-SIGN-related protein 1 (DC-SIGNR1). CD209b is an ~37 kDa type II transmembrane glycoprotein that is encoded by Cd209b (CD209b antigen) which belongs to the C-type lectin family. It contains a single C-terminal C-type lectin domain and is involved in the recognition of microbial polysaccharides. CD209b is expressed on macrophages residing in the splenic marginal zone, the medullary and trabecular sinuses of lymph nodes, and peritoneal cavity. CD209b is involved in the clearance and innate immune responses to microbial molecules including polysaccharides and lipopolysaccharides (LPS) and the uptake of encapsulated microbes. It may also affect leucocyte migration through its adhesive interaction with CD54 (ICAM-2).
Development References (7)
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Dijkstra CD, Van Vliet E, Döpp EA, van der Lelij AA, Kraal G. Marginal zone macrophages identified by a monoclonal antibody: characterization of immuno- and enzyme-histochemical properties and functional capacities.. Immunology. 1985; 55(1):23-30. (Clone-specific: Immunohistochemistry). View Reference
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Geijtenbeek TB, Groot PC, Nolte MA, et al. Marginal zone macrophages express a murine homologue of DC-SIGN that captures blood-borne antigens in vivo.. Blood. 2002; 100(8):2908-16. (Clone-specific: ELISA, Flow cytometry). View Reference
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Karlsson MC, Guinamard R, Bolland S, Sankala M, Steinman RM, Ravetch JV. Macrophages control the retention and trafficking of B lymphocytes in the splenic marginal zone.. J Exp Med. 2003; 198(2):333-40. (Clone-specific: Immunohistochemistry). View Reference
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Leenen PJ, de Bruijn MF, Voerman JS, Campbell PA, van Ewijk W. Markers of mouse macrophage development detected by monoclonal antibodies. J Immunol Methods. 1994; 174(1-2):5-19. (Clone-specific). View Reference
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Ravishankar B, Liu H, Shinde R, et al. The amino acid sensor GCN2 inhibits inflammatory responses to apoptotic cells promoting tolerance and suppressing systemic autoimmunity.. Proc Natl Acad Sci U S A. 2015; 112(34):10774-9. (Clone-specific: Flow cytometry, Fluorescence activated cell sorting). View Reference
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Van Vliet E, Melis M, Van Ewijk W. Monoclonal antibodies to stromal cell types of the mouse thymus.. Eur J Immunol. 1984; 14(6):524-9. (Immunogen: Immunohistochemistry). View Reference
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van Vliet E, Melis M, van Ewijk W. Marginal zone macrophages in the mouse spleen identified by a monoclonal antibody. Anatomical correlation with a B cell subpopulation.. J Histochem Cytochem. 1985; 33(1):40-4. (Immunogen: Immunohistochemistry). View Reference
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For Research Use Only. Not for use in diagnostic or therapeutic procedures.