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Recombinant Human Complement component C7 (C7), Truncated

ACP24220

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP24220 Target NameC7
Target SynonymsC7; CO7_HUMAN; complement component 7; Complement component C7FormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Protein LengthPartial
Purity>85% (SDS-PAGE)Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDP10643
Background Information
  • Uniprot Id

    P10643

  • Target Species

    Human

  • Target Name

    C7

  • Target Full Name

    Complement component C7

  • Target Function

    Constituent of the membrane attack complex (MAC) that plays a key role in the innate and adaptive immune response by forming pores in the plasma membrane of target cells. C7 serves as a membrane anchor.

  • Target Involvement

    Complement component 7 deficiency (C7D)

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    Complement C6/C7/C8/C9 family

  • Target Synonyms

    C7; CO7_HUMAN; complement component 7; Complement component C7

  • Target Background

    This gene encodes a serum glycoprotein that forms a membrane attack complex together with complement components C5b, C6, C8, and C9 as part of the terminal complement pathway of the innate immune system. The protein encoded by this gene contains a cholesterol-dependent cytolysin/membrane attack complex/perforin-like (CDC/MACPF) domain and belongs to a large family of structurally related molecules that form pores involved in host immunity and bacterial pathogenesis. This protein initiates membrane attack complex formation by binding the C5b-C6 subcomplex and inserts into the phospholipid bilayer, serving as a membrane anchor. Mutations in this gene are associated with a rare disorder called C7 deficiency.

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