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Complement C2/C2/Complement C2

a fragment Antibody Blocking Peptide(bs-8613P)-500ug
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  • bs-8613P
  • 2025年10月16日
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      500ug

    产品编号bs-8613P
    英文名称Complement C2/C2/Complement C2a fragment Antibody Blocking Peptide
    中文名称补体C2封闭多肽
    英文别名Complement C2; Complement component 2; Complement factor 2; Complement C2a fragment; CO2_HUMAN.
    纯化方法HPLC
    研究领域

    Immunology > Innate Immunity > Complement > Classical Pathway

    亚基C2a interacts with Schistosoma haematobium TOR (viaN-terminal extracellular domain). This results in inhibition of theclassical and lectin pathway of complement activation, probably dueto interference with binding of C2a to C4b such that C3 convertasecannot be formed. This infers resistance to complement-mediatedcell lysis, allowing parasite survival and infection.
    亚细胞定位Secreted.
    相似性Belongs to the peptidase S1 family.
    Contains 1 peptidase S1 domain.
    Contains 3 Sushi (CCP/SCR) domains.
    Contains 1 VWFA domain.
    功能Component C2 which is part of the classical pathway ofthe complement system is cleaved by activated factor C1 into twofragments: C2b and C2a. C2a, a serine protease, then combines withcomplement factor 4b to generate the C3 or C5 convertase.
    保存条件Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料

    bs-10482P is one synthetic peptide derived from human C2a.

    Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system. Activated C1 cleaves C2 into C2a and C2b. The serine proteinase C2a then combines with complement factor 4b to create the C3 or C5 convertase. Deficiency of C2 has been reported to associated with certain autoimmune diseases and SNPs in this gene have been associated with altered susceptibility to age-related macular degeneration. This gene localizes within the class III region of the MHC on the short arm of chromosome 6. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described in publications but their full-length sequence has not been determined.[provided by RefSeq, Mar 2009].

     

     

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