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宿主来源
Mouse抗原名称
IL-9R (CD129)分子别名
Interleukin-9 receptor; IL-9 receptor; IL-9R; CD129; IL9R细胞定位
Secreted, Cell membraneAccession
Q01113克隆号
S-3903抗体类型
Mouse mAb抗体同种型
IgG2b,k反应种属 ?
Hu阳性样本
HuT-78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
Interleukin-9 receptor (IL-9R), also designated as CD129, is a type I transmembrane protein that functions as the specific alpha subunit of the receptor complex for interleukin-9 (IL-9), a multifunctional cytokine primarily associated with Th9 cell responses and allergic inflammation. Structurally, IL-9R consists of an extracellular domain responsible for ligand binding, a single transmembrane helix, and an intracellular domain that lacks intrinsic kinase activity but recruits the common gamma chain (γc, CD132) to form a high-affinity signaling complex; upon IL-9 binding, this heterodimeric assembly activates the Janus kinase (JAK)/Signal Transducer and Activator of Transcription (STAT) pathway, predominantly triggering the phosphorylation of JAK1, JAK3, STAT1, STAT3, and STAT5, which subsequently modulates gene expression involved in cell proliferation, survival, and differentiation. Biologically, IL-9R expression is observed on various hematopoietic cells, including T cells, mast cells, eosinophils, and epithelial cells, playing a critical role in host defense against parasitic infections while simultaneously contributing to the pathogenesis of asthma, atopic dermatitis, and certain malignancies, thereby making it a significant target for therapeutic interventions aimed at inhibiting aberrant immune responses.
流式分析
Flow cytometric analysis of Human IL-9R (CD129) expression on HuT-78(human sezary syndrome cutaneous T lymphocyte). HuT-78 were stained with Biotin mouse IgG2b, k Isotype Control (black line histogram) or SDT Biotin Mouse Anti-Human IL-9R (CD129) Antibody (red line histogram) at 5μl/test followed by Sav-APC. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.







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