Flow cytometric analysis of C57BL/6 mouse bone marrow labelled Mouse CD200R3 antibody at 1/200 dilution (1 μg) / (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. Then cells were stained with CD49b – APC antibody separately. Total viable cells, as determined by Fixable Viability Dye 452 (S0D0021), were used for analysis. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.
Product Details
Product Details
Product Specification
| Host | Rat |
| Antigen | CD200R3 |
| Synonyms | Cell surface glycoprotein CD200 receptor 3; CD200 cell surface glycoprotein receptor-like 3 (CD200 receptor-like 3); CD200 cell surface glycoprotein receptor-like b (CD200RLb); Cell surface glycoprotein OX2 receptor 3; Cd200rlb; Cd200r3 |
| Location | Membrane |
| Accession | Q5UKY4 |
| Clone Number | Ba13 |
| Antibody Type | Rat mAb |
| Isotype | IgG2a,k |
| Application | FCM |
| Reactivity | Ms |
| Positive Sample | C57BL/6 mouse bone marrow |
| 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 |
| FCM | 1:200 | Ms |
Background
CD200R3, also known as CD200 receptor 3 or CMRF-35-like molecule 1 (CLM-1), is an inhibitory immunoreceptor belonging to the immunoglobulin superfamily that is primarily expressed on myeloid cells such as macrophages, dendritic cells, and granulocytes. Structurally characterized by two extracellular immunoglobulin-like domains and a cytoplasmic tail containing immunoreceptor tyrosine-based inhibitory motifs (ITIMs), CD200R3 functions as a critical negative regulator of innate immune responses by binding to its ligand, CD200 (OX-2), which is widely expressed on various cell types including neurons and endothelial cells. Upon ligand engagement, the receptor's ITIMs become phosphorylated, recruiting phosphatases like SHP-1 and SHP-2 to dampen downstream signaling cascades, thereby suppressing pro-inflammatory cytokine production, limiting excessive immune activation, and maintaining tissue homeostasis, particularly in contexts such as neuroinflammation, tumor microenvironments, and the prevention of autoimmunity.
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