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宿主来源
Rabbit抗原名称
CD163分子别名
Scavenger receptor cysteine-rich type 1 protein M130; Hemoglobin scavenger receptor; M130免疫原
Synthetic Peptide细胞定位
Secreted, Cell membraneAccession
Q86VB7克隆号
S-222-171抗体类型
Recombinant mAb抗体同种型
IgG反应种属 ?
Hu阳性样本
Human PBMC纯化方式
Protein A浓度
0.2 mg/ml标记
Biotin性状
Liquid缓冲体系
PBS pH7.4, 0.03% Proclin 300
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 5μl per million cells in 100μl volume Hu
CD163 is a type I transmembrane glycoprotein primarily expressed on the surface of monocytes and macrophages, belonging to the scavenger receptor cysteine-rich superfamily, class B. It plays a crucial role as a "clean-up" agent and immune regulator within the body. Its core function is the specific recognition and binding of the hemoglobin-haptoglobin complex, which is subsequently cleared via endocytosis by macrophages. This process protects tissues from oxidative damage caused by free hemoglobin and facilitates iron recycling. Furthermore, CD163 is recognized as a specific marker for M2 macrophages or tumor-associated macrophages. The function of CD163 is finely regulated; its membrane-bound form can be cleaved by metalloproteinases, releasing a soluble form (sCD163) into the bloodstream. Elevated levels of sCD163 serve as a biomarker for various inflammatory diseases. Recent research has also revealed that CD163 undergoes calcium concentration-dependent oligomerization via its SRCR domains, forming dimers or trimers, which is essential for its efficient ligand binding and subsequent endocytosis.
流式分析
Flow cytometric analysis of Human CD163 expression on Human PBMC (human peripheral blood mononuclear cells). Human PBMC were stained with Brilliant Violet 421™ Mouse Anti-Human CD14 antibody and either Biotin Rabbit IgG Isotype Control (Left panel) or SDT Biotin Rabbit Anti-Human CD163 Antibody (Right panel) at 5 μl/test followed by Sav-PE. Total viable cells, as determined by Fixable Viability Dye 515 (S0D0013), were used for analysis. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.







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