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宿主来源
Mouse抗原名称
CD182分子别名
C-X-C chemokine receptor type 2; CXC-R2; CXCR-2; CDw128b; GRO/MGSA receptor; High affinity interleukin-8 receptor B (IL-8R B); IL-8 receptor type 2; IL8RB; CXCR2细胞定位
Cell membraneAccession
P25025克隆号
S-4787抗体类型
Mouse mAb抗体同种型
IgG1,λ反应种属 ?
Hu阳性样本
Human peripheral blood cells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 1:400 Hu
CD182, also known as C-X-C chemokine receptor type 2 (CXCR2) or IL-8 receptor beta, is a seven-transmembrane G protein-coupled receptor (GPCR) encoded by 11 exons, located on human chromosome 2q35, with a molecular weight of approximately 67-70 kDa. This receptor is primarily expressed on the surface of neutrophils, NK cells, monocytes, mast cells, and some T cells, and binds to its high-affinity ligands (such as IL-8, CXCL1, CXCL2, CXCL3, etc.). Upon activation, CD182 mediates intracellular signaling via G proteins, primarily driving the chemotactic migration of neutrophils and other immune cells to sites of inflammation, while also playing key roles in regulating cell activation, proliferation, and angiogenesis. In terms of pathophysiology, CD182 is not only involved in host immune surveillance against infections but also closely associated with tumor immune escape—within the tumor microenvironment, the CXCR2 signaling axis promotes the recruitment of immunosuppressive cells such as myeloid-derived suppressor cells (MDSCs) and regulates the polarization of tumor-associated macrophages (TAMs), thereby inhibiting anti-tumor immune responses and promoting tumor growth and metastasis. Therefore, CD182 has become an important potential target for drug development in cancer immunotherapy and chronic inflammatory diseases.
流式分析
Flow cytometric analysis of human peripheral blood cells labeled with anti - Human CD182 antibody at 1/400 dilution (0.5 μg) / (right panel) compared with a Mouse IgG1,λ Isotype Control / (left panel). Goat Anti-Mouse IgG Alexa Fluor® 647 was used as the secondary antibody. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.







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