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R718 Rat Anti-Mouse CD209b (SIGN-R1)
R718 Rat Anti-Mouse CD209b (SIGN-R1)
Multiparameter flow cytometric analysis of CD209b (SIGN-R1) expression on viable 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 and were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™) [Cat. No. 553142]. The cells were stained with BD Horizon™ BV421 Rat Anti-CD11b antibody (Cat. No. 562605) and with either BD Horizon™ R718 Rat IgM, κ Isotype Control (Cat. No. 566950; Left Plot) or BD Horizon™ R718 Rat Anti-Mouse CD209b (SIGN-R1) antibody (Cat. No. 570049/570130; Right Plot) at 0.5 µg/test. BD Via-Probe™ Cell Viability 7-AAD Solution (Cat. No. 555815/555816) was added to cells right before analysis. The bivariate pseudocolor density plots showing the correlated expression of CD209b (SIGN-R1) [or Ig Isotype control staining] versus CD11b were derived from gated events with the forward and side-light scatter characteristics of viable (7-AAD-negative) PECs. Flow cytometry and data analysis were performed using a BD LSRFortessa™ X-20 Cell Analyzer System and FlowJo™ Software. Data shown on this Technical Data Sheet are not lot specific.
Multiparameter flow cytometric analysis of CD209b (SIGN-R1) expression on viable 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 and were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™) [Cat. No. 553142]. The cells were stained with BD Horizon™ BV421 Rat Anti-CD11b antibody (Cat. No. 562605) and with either BD Horizon™ R718 Rat IgM, κ Isotype Control (Cat. No. 566950; Left Plot) or BD Horizon™ R718 Rat Anti-Mouse CD209b (SIGN-R1) antibody (Cat. No. 570049/570130; Right Plot) at 0.5 µg/test. BD Via-Probe™ Cell Viability 7-AAD Solution (Cat. No. 555815/555816) was added to cells right before analysis. The bivariate pseudocolor density plots showing the correlated expression of CD209b (SIGN-R1) [or Ig Isotype control staining] versus CD11b were derived from gated events with the forward and side-light scatter characteristics of viable (7-AAD-negative) PECs. Flow cytometry and data analysis were performed using a BD LSRFortessa™ X-20 Cell Analyzer System and FlowJo™ Software. Data shown on this Technical Data Sheet are not lot specific.
Product Details
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BD Horizon™
Cd209b; DC-SIGN-related protein 1; DC-SIGNR1; SIGNR1; mSIGNR1
Mouse (QC Testing)
Rat LOU, also known as Louvain, LOU/C, LOU/M IgM, κ
C3H Mouse Thymic Stromal Cells
Flow cytometry (Routinely Tested)
0.2 mg/ml
69165
Aqueous buffered solution containing ≤0.09% sodium azide.
RUO


Preparation And Storage

The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. The antibody was conjugated to the dye under optimum conditions and unreacted dye was removed. Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze.

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 cells and BD® CompBeads to ensure that BD® CompBeads are appropriate for your specific cellular application.

Product Notices

  1. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
  2. 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.
  3. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
  4. For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
  5. An isotype control should be used at the same concentration as the antibody of interest.
  6. Please refer to http://regdocs.bd.com to access safety data sheets (SDS).
  7. This product is provided under an Agreement between BIOTIUM and BD Biosciences. This product, and only in the amount purchased by buyer, may be used solely for buyer’s own internal research, in a manner consistent with the accompanying product literature. No other right to use, sell or otherwise transfer (a) this product, or (b) its components is hereby granted expressly, by implication or by estoppel. This product is for research use only. Diagnostic uses require a separate license from Biotium, Inc. For information on purchasing a license to this product including for purposes other than research, contact Biotium, Inc., 3159 Corporate Place, Hayward, CA 94545, Tel: (510) 265-1027. Fax: (510) 265-1352. Email: btinfo@biotium.com.
  8. Alexa Fluor™ is a trademark of Life Technologies Corporation.
  9. For U.S. patents that may apply, see bd.com/patents.
570049 Rev. 1
Antibody Details
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ER-TR9

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).

570049 Rev. 1
Format Details
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R718
The BD Horizon™ Red 718 (R718) Dye is part of the BD red family of dyes. It is a small organic fluorochrome with an excitation maximum (Ex Max) at 695-nm and an emission maximum (Em Max) at 718-nm. Driven by BD innovation, R718 is designed to be excited by the red laser (627–640-nm) and detected using an optical filter centered near 720-nm (e.g., a 720/40-nm bandpass filter). R718 is a brighter alternative to Alexa Fluor™ 700. R718 is also a bright small molecule alternative to APC-R700 with lower spread into the APC detector. Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
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R718
Red 627-640 nm
695 nm
718 nm
570049 Rev.1
Citations & References
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View product citations for antibody "570049" on CiteAb

Development References (7)

  1. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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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570049 Rev. 1

 

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