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宿主来源
Mouse抗原名称
CD125分子别名
Interleukin-5 receptor subunit alpha; IL-5 receptor subunit alpha; IL-5R subunit alpha; IL-5R-alpha; IL-5RAAlternative nameCDw125; IL5R; IL5RA细胞定位
MembraneAccession
Q01344克隆号
S-4480抗体类型
Mouse mAb抗体同种型
IgG1,k同型对照
S0B5431反应种属 ?
Hu阳性样本
Human peripheral blood cells纯化方式
Protein G浓度
0.2 mg/ml标记
Biotin性状
Liquid缓冲体系
PBS pH7.4, 0.09% sodium azide
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
CD125, also known as the interleukin-4 receptor subunit alpha (IL-4Rα), is a type I transmembrane protein that serves as a critical shared signaling component for both the type I and type II interleukin-4 receptors, thereby playing a pivotal role in regulating immune responses, particularly those associated with Th2-mediated inflammation, allergic reactions, and asthma. As the primary binding subunit for interleukin-4 (IL-4) and interleukin-13 (IL-13), CD125 facilitates the activation of downstream signaling pathways, most notably the JAK-STAT pathway (specifically JAK1/STAT6), which leads to the transcription of genes involved in IgE class switching, eosinophil recruitment, mucus production, and alternative macrophage activation. Structurally, it consists of an extracellular domain responsible for cytokine binding, a single transmembrane helix, and a cytoplasmic tail containing specific motifs that recruit Janus kinases, making it a significant therapeutic target; indeed, monoclonal antibodies such as dupilumab specifically inhibit the interaction of IL-4 and IL-13 with CD125 to effectively treat moderate-to-severe atopic dermatitis, asthma, and chronic rhinosinusitis with nasal polyps by blocking this central axis of type 2 inflammatory signaling.
流式分析
Flow cytometric analysis of human CD125 expression on human peripheral blood cells. Human peripheral blood cells were stained with either Biotin Mouse IgG1, k Isotype Control (left panel) or SDT Biotin Mouse Anti-Human CD125 Antibody (right panel) at 5 μl/test followed by Sav-APC. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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