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宿主来源
Mouse抗原名称
CD119分子别名
Interferon gamma receptor 1; IFN-gamma receptor 1; IFN-gamma-R1; CDw119; Interferon gamma receptor alpha-chain; IFNGR1细胞定位
Cell membraneAccession
P15260克隆号
S-3124抗体类型
Mouse mAb抗体同种型
IgG2b,k反应种属 ?
Hu阳性样本
Human Peripheral Blood cells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
CD119 protein, also known as interferon-gamma receptor alpha chain (IFN-γRα), is a critical member of the type II cytokine receptor family on the cell surface. It serves as the high-affinity and specific binding subunit for interferon-gamma (IFN-γ) and, together with the β chain (IFN-γRβ), forms the functional receptor dimer responsible for recognizing and transmitting IFN-γ signals. IFN-γ is primarily produced by activated T cells and natural killer cells and is a central cytokine regulating both innate and adaptive immunity. Upon binding of IFN-γ, CD119 induces receptor subunit aggregation and activates the associated JAK1/JAK2 kinases, leading to phosphorylation of the STAT1 transcription factor. Activated STAT1 forms homodimers and translocates into the nucleus, driving the expression of a wide array of interferon-stimulated genes (ISGs). This process promotes macrophage activation, enhances antigen presentation, facilitates Th1-type immune responses, and exerts potent antiviral and anti-intracellular pathogen effects. CD119 is expressed on various immune cells (such as macrophages, T cells, and NK cells) as well as non-immune cells. Loss-of-function mutations in CD119 can lead to a severe hereditary immunodeficiency known as Mendelian susceptibility to mycobacterial disease (MSMD), rendering patients susceptible to weakly virulent mycobacteria and certain viruses. Therefore, CD119 acts not only as a key sentinel in immune defense but also as an important target for immunomodulation and the treatment of infectious diseases.
流式分析
Flow cytometric analysis of human CD119 expression on human peripheral blood cells. Human peripheral blood cells were stained with either Biotin IgG2b, k Isotype Control (left panel) or SDT Biotin Mouse Anti-Human CD119 Antibody (right panel) at 5 μl/test followed by Sav-PE. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.







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