Human MMR/CD206 Antibody

(6 citations)   
  • Species Reactivity
    Human
  • Specificity
    Detects human MMR/CD206 in direct ELISAs and Western blots. In direct ELISAs, approximately 20% cross-reactivity with recombinant mouse MMR is observed.
  • Source
    Polyclonal Goat IgG
  • Purification
    Antigen Affinity-purified
  • Immunogen
    Mouse myeloma cell line NS0-derived recombinant human MMR/CD206
    Leu19-Lys1383 (Thr399Ala) & (Leu407Phe)
    Accession # P22897
  • Formulation
    Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied as a 0.2 µm filtered solution in PBS.
  • Label
    Unconjugated
Applications
  •  
    Recommended
    Concentration
    Sample
  • Western Blot
    1 µg/mL
    See below
  • Immunocytochemistry
    5-15 µg/mL
    Immersion fixed human peripheral blood mononuclear cells
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Data Examples
Detection of Human MMR/CD206 by Western Blot. Western blot shows lysates of human immature dendritic cells. PVDF Membrane was probed with 1 µg/mL of Goat Anti-Human MMR/CD206 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2534) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # HAF019). A specific band was detected for MMR/CD206 at approximately 185 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 8.
Preparation and Storage
  • Reconstitution
    Reconstitute at 0.2 mg/mL in sterile PBS.
  • Shipping
    The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. *Small pack size (SP) is shipped with polar packs. Upon receipt, store it immediately at -20 to -70 °C
  • Stability & Storage
    Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
    • 12 months from date of receipt, -20 to -70 °C as supplied.
    • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
    • 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: MMR/CD206

The human Macrophage Mannose Receptor (MMR), also known as CD206 and MRC1 (mannose receptor C, type 1), is a 190 kDa scavenger receptor that is expressed on tissue macrophages, myeloid dendritic cells, and liver and lymphatic endothelial cells (1). It belongs to a family of receptors sharing similar protein structure that also includes DEC205, phospholipase A2 receptor, and Endo180 (2, 3). The human MMR protein is synthesized as a 1456 amino acid (aa) precursor that contains an 18 aa signal sequence, a 1371 aa extracellular region, a 21 aa transmembrane segment and a 46 aa cytoplasmic domain (4). Its extracellular region is composed of an N‑terminal cysteine-rich domain, followed by a single fibronectin type II repeat, and eight C-type lectin carbohydrate recognition domains (CRD) (3, 4). Human to mouse, the extracellular region is 82% aa identical. The cysteine-rich domain mediates recognition of sulfated N‑acetylgalactosamine, which occurs on some extracellular matrix proteins and is the terminal sugar of the unusual oligosaccharides present on pituitary hormones such as lutropin and thyrotropin (5). Several of the CRDs participate in the Ca2+-dependent recognition of carbohydrates showing a preference for branched sugars with terminal mannose, fucose or N‑acetylglucosamine (6). The cytoplasmic domain of MMR includes a tyrosine-based motif for internalization in clathrin-coated vesicles. Once internalized, ligands are released following acidification of phagosomes or endosomes, and the receptor is recycled to the cell surface (3, 7). MMR mediates phagocytosis upon binding to target structures that occur on a variety of pathogenic microorganisms including Gram-negative and Gram-positive bacteria, yeasts, parasites, and mycobacteria. MMR also functions to maintain homeostasis through the endocytosis of potentially harmful glycoproteins associated with inflammation (2, 3).

  • References:
    1. East, L. and C. Isake (2002) Biochim. Biophys. Acta 1572:364. 
    2. Chieppa, M. et al. (2003) J. Immunol. 171:4552. 
    3. Figdor, C. et al. (2002) Nat. Rev. Immunol. 2:77.
    4. Taylor, M. et al. (1990) J. Biol. Chem. 265:12156.
    5. Leteux, C. et al. (2000) J. Exp. Med. 191:1117.
    6. Martinez-Pomares, L. et al. (2001) Immunobiology 204:527.
    7. Feinberg, H. et al. (2000) J. Biol. Chem. 275:21539.
  • Long Name:
    Macrophage Mannose Receptor
  • Entrez Gene IDs:
    4360 (Human); 17533 (Mouse); 291327 (Rat)
  • Alternate Names:
    CD206; CLEC13D; CLEC13Dmacrophage mannose receptor 1; C-type lectin domain family 13 member D; mannose receptor, C type 1; MMR; MMRCD206 antigen; MRC1
Related Research Areas
Citations:

R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.

6 Citations: Showing 1 - 6
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Species
Applications
Sample Type
  1. Regulatory role of cytosolic phospholipase A2 alpha in the induction of CD40 in microglia
    Authors: YF Malada-Ede, N Hadad, R Levy
    J Neuroinflammation, 2017;14(1):33.
    Species: Mouse
    Sample Type: Whole Tissue
    Application: IHC
  2. FITC Conjugation Markedly Enhances Hepatic Clearance of N-Formyl Peptides
    PLoS ONE, 2016;11(8):e0160602.
    Species: Human
    Sample Type: Whole Tissue
    Application: IHC OCT-embedded
  3. MicroRNA29a regulates IL-33-mediated tissue remodelling in tendon disease.
    Authors: Millar N, Gilchrist D, Akbar M, Reilly J, Kerr S, Campbell A, Murrell G, Liew F, Kurowska-Stolarska M, McInnes I
    Nat Commun, 2015;6(0):6774.
    Species: Human
    Sample Type: Whole Tissue
    Application: IHC Not Specified
  4. Pioglitazone treatment reduces adipose tissue inflammation through reduction of mast cell and macrophage number and by improving vascularity.
    Authors: Spencer M, Yang L, Adu A, Finlin B, Zhu B, Shipp L, Rasouli N, Peterson C, Kern P
    PLoS ONE, 2014;9(7):e102190.
    Species: Human
    Sample Type: Whole Tissue
    Application: IHC - Paraffin embedded
  5. Targeting the ANG2/TIE2 axis inhibits tumor growth and metastasis by impairing angiogenesis and disabling rebounds of proangiogenic myeloid cells.
    Authors: Mazzieri R, Pucci F, Moi D, Zonari E, Ranghetti A, Berti A, Politi LS, Gentner B, Brown JL, Naldini L, De Palma M
    Cancer Cell, 2011;19(4):512-26.
    Species: Mouse
    Sample Type: Whole Tissue
    Application: IHC
  6. Acid fibroblast growth factor and peripheral nerve grafts regulate Th2 cytokine expression, macrophage activation, polyamine synthesis, and neurotrophin expression in transected rat spinal cords.
    Authors: Kuo HS, Tsai MJ, Huang MC
    J. Neurosci., 2011;31(11):4137-47.
    Species: Rat
    Sample Type: Whole Tissue
    Application: IHC
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