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        human IL-6 Mouse mAb (V0401)  
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        產品編號 V0401
        英文名稱 human IL-6 Mouse mAb
        中文名稱 人白介素6單克隆抗體
        別    名 Interleukin BSF 2; B cell differentiation factor; B cell stimulatory factor 2; BSF 2; BSF2; CDF; CTL differentiation factor; Cytotoxic T cell differentiation factor; Hepatocyte stimulating factor; HGF; HPGF; HSF; Hybridoma growth factor; Hybridoma plasmacytoma growth factor; IFNB2; IL 6; IL6 protein; Interferon beta 2; Interleukin 6 (interferon beta 2); Interleukin 6; Interleukin-6; Interleukin6; IL6_HUMAN.  
        克 隆 號 6F5K
        理論分子量 23 kDa
        檢測分子量
        細胞定位 分泌型蛋白 
        性    狀 Liquid
        濃    度 ≥1mg/ml
        緩 沖 液 0.01M PBS (pH7.4) with 0.02% Proclin300.
        保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
        注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
        產品介紹 Interleukin 6 (IL-6), promptly and transiently produced in response to infections and tissue injuries, contributes to host defense through the stimulation of acute phase responses, hematopoiesis, and immune reactions.

        Function:
        Cytokine with a wide variety of biological functions. It is a potent inducer of the acute phase response. Plays an essential role in the final differentiation of B-cells into Ig-secreting cells Involved in lymphocyte and monocyte differentiation. It induces myeloma and plasmacytoma growth and induces nerve cells differentiation Acts on B-cells, T-cells, hepatocytes, hematopoietic progenitor cells and cells of the CNS. Also acts as a myokine. It is discharged into the bloodstream after muscle contraction and acts to increase the breakdown of fats and to improve insulin resistance.

        Subcellular Location:
        Secreted.

        Post-translational modifications:
        N- and O-glycosylated.

        DISEASE:
        Genetic variations in IL6 are associated with susceptibility to rheumatoid arthritis systemic juvenile (RASJ) [MIM:604302]. An inflammatory articular disorder with systemic-onset beginning before the age of 16. It represents a subgroup of juvenile arthritis associated with severe extraarticular features and occasionally fatal complications. During active phases of the disorder, patients display a typical daily spiking fever, an evanescent macular rash, lymphadenopathy, hepatosplenomegaly, serositis, myalgia and arthritis.
        Note=A IL6 promoter polymorphism is associated with a lifetime risk of development of Kaposi sarcoma in HIV-infected men.

        Similarity:
        Belongs to the IL-6 superfamily.

        Gene ID:
        3569

        Database links:

        Entrez Gene: 3569 Human

        Entrez Gene: 16193 Mouse

        Entrez Gene: 24498 Rat

        Omim: 147620 Human

        SwissProt: P05231 Human

        SwissProt: P08505 Mouse

        SwissProt: P20607 Rat

        Unigene: 654458 Human

        Unigene: 1019 Mouse

        Unigene: 9873 Rat



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