RAW 264.7 mouse monocyte/macrophage cell line was stained with Rat Anti-Mouse SR-AI/MSR Fluorescein-conjugated Monoclonal Antibody (Catalog # FAB1797F, filled histogram) or isotype control antibody (Catalog # IC013F, ...read more
Detects mouse SR‑AI/MSR in direct ELISAs and Western blots. In direct ELISAs and Western blots, no cross‑reactivity with recombinant human SR-AI is observed.
Source
N/A
Isotype
IgG2b
Clonality
Monoclonal
Host
Rat
Gene
MSR1
Purity Statement
Protein A or G purified from hybridoma culture supernatant
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Store the unopened product at 2 - 8° C. Do not use past expiration date. Protect from light.
Buffer
Supplied in a saline solution containing BSA and Sodium Azide.
Preservative
Sodium Azide
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for SR-AI/MSR Antibody (268318) [Fluorescein]
CD204 antigen
CD204
Macrophage acetylated LDL receptor I and II
macrophage scavenger receptor 1
macrophage scavenger receptor type III
MSR1
phSR1
phSR2
SCARA1
SCARA1macrophage scavenger receptor types I and II
Scavenger receptor class A member 1
scavenger receptor class A, member 1
SR-A
SRAI
SR-AI
Background
The Scavenger Receptor (SR) family comprises a group of functionally defined membrane receptors that share the common ability to bind and internalize modified forms of Low Density Lipoproteins (mLDL) (1‑3). Family members are classified alphabetically. The A class includes four proteins: the three subtypes of SR-A (AI, AII, and AIII) that are generated by alternative splicing of the same gene, and a structurally similar protein named MARCO (4). All A class SRs are multidomain, trimeric type II trans-membrane proteins. SR-AI has an N-terminal cytoplasmic domain, a transmembrane domain, a spacer domain, an alpha -helical coiled coil, a collagen-like domain and a C-terminal cysteine-rich domain. SR-A is expressed by most tissue macrophages, dendritic cells and Kupffer cells. It is also highly expressed by microglia in neonatal as well as Alzheimer’ Disease brains. SR-AI binds a broad range of polyanionic ligands including modified proteins (e.g. oxidized, acetylated or maleylated LDL, advanced glycation end-product proteins), polyribonucleotides (polyguanosine and polyinosine), polysaccharides (dextran sulfate, fucoidan), phospholipids (phosphatidylserine), bacterial products (lipopolysaccharide and lipoteichoic acid) and selected chemical compounds (silica, crocidolite asbestos). The ligand-binding region has been localized to a positively charged region in the carboxyl end of the collagen-like domain. Based on its ligand binding characteristics, SR-AI is implicated in many physiological and pathophysiological functions. Studies using SR-A knockout mouse have also suggested roles of SR-A in atherogenesis, host defense and innate immunity, acquired immune responses, macrophage adhesion, and phagocytosis of apoptotic cells (1‑3). Over aa 83-458, mouse and human SR-AI share 71% amino acid sequence identity.
Daugherty, A. et al. (2000) Curr. Opin. Cardiovasc. Pulm. Ren. Invest. Drugs 2:223.
Platt, N. and S. Gordon (2001) J. Clin. Invest. 108:649.
Platt, N. and S. Gordon (1998) Chem. Biol. 5:R193.
Elomaa, O. et al. (1995) Cell 80:603.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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