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Rat Anti-Mouse CD206 (MMR) Antibody (S-R498)

Rat Anti-Mouse CD206 (MMR) Antibody (S-R498)

Catalog Number: S0B1295 Application: FCM Reactivity: Mouse Conjugation: Unconjugated Brand: Starter
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Regular price $130.00 SGD
Regular price Sale price $130.00 SGD
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Product Details

Product Specification


Host Rat
Antigen Mouse CD206
Synonyms Macrophage mannose receptor 1; Mrc1
Location Cell membrane
Accession Q61830
Clone Number S-R498
Antibody Type Rat mAb
Isotype IgG2a,k
Application ICFCM
Reactivity Ms
Positive Sample Mouse resident peritoneal exudate cells
Purification Protein G
Concentration 2 mg/ml
Conjugation Unconjugated
Physical Appearance Liquid
Storage Buffer

PBS pH7.4

Stability & Storage

12 months from date of receipt / reconstitution, 2 to 8 °C as supplied

Dilution


application dilution species
ICFCM 1:200 Ms

Background

CD206, also known as the mannose receptor, is a highly glycosylated type I transmembrane protein predominantly expressed on the surface of macrophages, dendritic cells, and endothelial cells in various tissues. It functions as an endocytic lectin receptor, mediating the internalization of soluble and particulate carbohydrate structures, thereby participating in innate immunity. CD206 plays a crucial role in the clearance of pathogens, apoptotic cell debris, and extracellular matrix components by binding to glycan structures such as N-acetylgalactosamine and glycosylated molecules. This receptor is also implicated in the regulation of inflammation, as it can inhibit the production of pro-inflammatory cytokines by macrophages and induce an anti-inflammatory phenotype. CD206 is highly specific and is considered a marker for M2-type macrophages, which are associated with tumor progression, including angiogenesis and tissue invasion. Its expression has been closely linked to various malignancies such as breast, ovarian, pancreatic, and prostate cancer, making it a significant target for research in understanding tumor immune microenvironments and for the development of targeted therapies.

Picture

FC

Mouse resident peritoneal exudate cells were surface stained with APC Rat Anti-Mouse F4/80 followed by fixation with 4% PFA and permeabilization with the 0.1% Tween. Cells were then intracellularly stained with Rat Anti-Mouse CD206 (MMR) Antibody at 1/200 (1 μg) dilution / (Right panel) compared with a Rat IgG2a, κ Isotype Control / (Left panel). Goat Anti-Rat IgG Alexa Fluor® 488 was used as the secondary antibody. Total cells were used for analysis.

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