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Recombinant Human Plasma kallikrein (KLKB1), Truncated

ACP09169

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP09169 Target NameKLKB1
FormLyophilized powderExpression SystemCustom Production. Please inquire and provide the desire expression system.
Expression Range20-390Protein 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 IDP03952
Background Information
  • Uniprot Id

    P03952

  • Target Species

    Human

  • Target Name

    KLKB1

  • Target Full Name

    Plasma kallikrein

  • Target Function

    The enzyme cleaves Lys-Arg and Arg-Ser bonds. It activates, in a reciprocal reaction, factor XII after its binding to a negatively charged surface. It also releases bradykinin from HMW kininogen and may also play a role in the renin-angiotensin system by converting prorenin into renin.

  • Target Involvement

    Prekallikrein deficiency (PKK deficiency)

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    Peptidase S1 family, Plasma kallikrein subfamily

  • Target Research Area

    Cell Biology

  • Target Synonyms

    Fletcher factor; kallikrein B plasma; Kallikrein B plasma (Fletcher factor) 1; Kallikrein B; plasma 1; Kallikrein B1; Kininogenin; KLK3; KLKB1; KLKB1_HUMAN; PKK; PKKD; Plasma kallikrein; Plasma kallikrein B1; Plasma kallikrein light chain; Plasma prekallikrein; PPK; Prekallikrein

  • Target Background

    This gene encodes a glycoprotein that participates in the surface-dependent activation of blood coagulation, fibrinolysis, kinin generation and inflammation. The encoded preproprotein present in plasma as a non-covalent complex with high molecular weight kininogen undergoes proteolytic processing mediated by activated coagulation factor XII to generate a disulfide-linked, heterodimeric serine protease comprised of heavy and light chains. Certain mutations in this gene cause prekallikrein deficiency. Alternative splicing results in multiple transcript variants encoding different isoforms.

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