Fibrinogen β Monoclonal Antibody

    • 货号:YM0268
    • 应用:WB;ELISA
    • 种属:Human
      • 靶点:
      • Fibrinogen β
      • 简介:
      • >>Complement and coagulation cascades;>>Platelet activation;>>Neutrophil extracellular trap formation;>>Coronavirus disease - COVID-19
      • 基因名称:
      • FGB
      • 蛋白名称:
      • Fibrinogen beta chain
      • Human Gene Id:
      • 2244
      • Human Swiss Prot No:
      • P02675
      • Mouse Swiss Prot No:
      • Q8K0E8
      • 免疫原:
      • Purified recombinant fragment of human Fibrinogen β (aa30-300) expressed in E. Coli.
      • 特异性:
      • Fibrinogen β Monoclonal Antibody detects endogenous levels of Fibrinogen β protein.
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Monoclonal, Mouse
      • 稀释:
      • WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.
      • 纯化工艺:
      • Affinity purification
      • 储存:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • 其他名称:
      • FGB;Fibrinogen beta chain
      • 分子量:
      • 56kD
      • 背景:
      • The protein encoded by this gene is the beta 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 afibrinogenemia, dysfibrinogenemia, hypodysfibrinogenemia and thrombotic tendency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014],
      • 功能:
      • disease:Defects in FGB are a cause of congenital afibrinogenemia [MIM:202400]. This rare autosomal recessive disorder is characterized by bleeding that varies from mild to severe and by complete absence or extremely low levels of plasma and platelet fibrinogen.,disease:Defects in FGB are a cause of thrombophilia.,domain:A long coiled coil structure formed by 3 polypeptide chains connects the central nodule to the C-terminal domains (distal nodules). The long C-terminal ends of the alpha chains fold back, contributing a fourth strand to the coiled coil structure.,function:Fibrinogen has a double function: yielding monomers that polymerize into fibrin and acting as a cofactor in platelet aggregation.,online information:Fibrinogen entry,online information:The Singapore human mutation and polymorphism database,PTM:Conversion of fibrinogen to fibrin is triggered by thrombin, which cleaves fib
      • 细胞定位:
      • Secreted .
      • 组织表达:
      • Detected in blood plasma (at protein level).
      • 产品图片
      • Western Blot analysis using Fibrinogen β Monoclonal Antibody against human plasma (1).