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FITC Rat Anti-Mouse CD206 Antibody(S-4793)

FITC Rat Anti-Mouse CD206 Antibody(S-4793)

Catalog Number: S0B80824 Application: FCM Reactivity: Ms Conjugation: FITC Brand: Starter
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Regular price $140 USD
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Product Details

Product Specification


Host Rat
Antigen CD206
Synonyms Macrophage mannose receptor 1; MMR; Mrc1
Location Endosome, Cell membrane
Accession Q61830
Clone Number S-4793
Antibody Type Rat mAb
Isotype IgG2a,k
Isotype Control S0B5453
Application FCM
Reactivity Ms
Positive Sample BALB/c mouse peritoneal exudates cells
Purification Protein G
Concentration 0.5 mg/ml
Conjugation FITC
Physical Appearance Liquid
Storage Buffer

PBS, 1% BSA, 0.09% sodium azide

Stability & Storage

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

Dilution


application dilution species
FCM 1μg per million cells in 100μl volume Hu

Background

CD206, also known as the mannose receptor (MR) or mannose receptor C type 1 (MRC1), is a transmembrane glycoprotein that belongs to the C-type lectin family. It is predominantly expressed by tissue macrophages, dendritic cells, and certain lymphatic or liver endothelial cells. CD206 recognizes and mediates endocytosis of pathogens by binding to glycoproteins terminated with mannose. This receptor serves as a homeostatic receptor by binding and scavenging unwanted high mannose N-linked glycoproteins as well as pituitary hormones from the circulation. In addition, CD206 is a marker for the M2 phenotype of macrophages, which are involved in immunosuppression, tissue remodeling, and Th2 effector responses. Its expression is regulated by various cytokines and is considered a marker of an M2-like macrophage phenotype.

Picture

FC

Flow cytometric analysis of Mouse CD206 (MMR) expression on BALB/c mouse peritoneal exudates cells. BALB/c mouse peritoneal exudates cells were stained with PE Rat Anti-Mouse CD107b Antibody and either FITC Rat IgG2a, κ Isotype Control (left panel) or SDT FITC Rat Anti-Mouse CD206 (MMR) Antibody (right panel) at 2 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.