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FGG 抗体

FGG 适用: 人, 小鼠, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7234438
发货至: 中国
  • 抗原 See all FGG 抗体
    FGG (Fibrinogen gamma Chain (FGG))
    适用
    • 78
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    人, 小鼠, 大鼠
    宿主
    • 77
    • 15
    • 4
    • 1
    克隆类型
    • 74
    • 23
    多克隆
    标记
    • 54
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    This FGG antibody is un-conjugated
    应用范围
    • 80
    • 29
    • 25
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    • 13
    • 8
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    Western Blotting (WB), Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen Affinity Purification
    免疫原
    Recombinant Mouse Fibrinogen gamma chain protein
    亚型
    IgG
    Top Product
    Discover our top product FGG Primary Antibody
  • 应用备注
    WB 1:1000-1:3000 IHC 1:100-1:300
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.05 % Proclin300, 50 % glycerol, pH 7.3
    储存液
    ProClin
    注意事项
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    FGG (Fibrinogen gamma Chain (FGG))
    别名
    FGG (FGG 产品)
    别名
    FXII antibody, HAF antibody, 3010002H13Rik antibody, AI256424 antibody, fibrinogen antibody, FGG antibody, LOC100220680 antibody, fb60h05 antibody, fb62e01 antibody, wu:fb60h05 antibody, wu:fb62e01 antibody, zgc:56023 antibody, fibrinogen gamma chain antibody, coagulation factor XII (Hageman factor) antibody, fibrinogen gamma chain L homeolog antibody, FGG antibody, F12 antibody, fgg antibody, Fgg antibody, fgg.L antibody, CpipJ_CPIJ006387 antibody, CpipJ_CPIJ010087 antibody
    背景
    The protein encoded by this gene is the gamma component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains. Following vascular injury, fibrinogen is cleaved by thrombin to form fibrin which is the most abundant component of blood clots. In addition, various cleavage products of fibrinogen and fibrin regulate cell adhesion and spreading, display vasoconstrictor and chemotactic activities, and are mitogens for several cell types. Mutations in this gene lead to several disorders, including dysfibrinogenemia, hypofibrinogenemia and thrombophilia. Alternative splicing results in transcript variants encoding different isoforms.
    分子量

    Observed_MW: 49 kDa

    Calculated_MW: 49 kDa

    基因ID
    99571
    UniProt
    Q8VCM7
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