Rat Anti-Mouse CD200R3 Antibody (Ba13)
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
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宿主来源
Rat抗原名称
CD200R3分子别名
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细胞定位
MembraneAccession
Q5UKY4克隆号
Ba13抗体类型
Rat mAb抗体同种型
IgG2a,k反应种属 ?
Ms阳性样本
C57BL/6 mouse bone marrow纯化方式
Protein G浓度
2 mg/ml标记
Unconjugated性状
Liquid缓冲体系
PBS pH7.4
储存条件
12 months from date of receipt / reconstitution, 2 to 8 °C as supplied
应用
FCM
稀释度
应用 稀释度 推荐种属 FCM 1:200 Ms
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.
流式分析
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.







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