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Recombinant Human Vitamin K-dependent protein C(PROC)

ACP00476

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP00476 Target NamePROC
Target SynonymsAnticoagulant protein C;Autoprothrombin IIA;Blood coagulation factor XIVFormLiquid or Lyophilized powder
Expression SystemE.coliExpression Range43-461aa
Mol Weight54.2 kDaProtein LengthFull Length of Mature Protein
PurityGreater than 95% as determined by 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 IDP04070
Background Information
  • Uniprot Id

    P04070

  • Target Species

    Human

  • Target Name

    PROC

  • Target Full Name

    Vitamin K-dependent protein C

  • Target Function

    Protein C is a vitamin K-dependent serine protease that regulates blood coagulation by inactivating factors Va and VIIIa in the presence of calcium ions and phospholipids. Exerts a protective effect on the endothelial cell barrier function.

  • Target Involvement

    Thrombophilia due to protein C deficiency, autosomal dominant (THPH3); Thrombophilia due to protein C deficiency, autosomal recessive (THPH4)

  • Target Subcellular Location

    Secreted. Golgi apparatus. Endoplasmic reticulum.

  • Target Protein Families

    Peptidase S1 family

  • Target Tissue Specificity

    Plasma; synthesized in the liver.

  • Target Research Area

    Others

  • Target Synonyms

    Activation peptide; Anticoagulant protein C; APC; Autoprothrombin IIA; Blood coagulation factor XIV; EC 3.4.21.69; PC; proC; PROC_HUMAN; PROC1 ; Protein C (inactivator of coagulation factors Va and VIIIa); THPH3; THPH4; Vitamin K dependent protein C

  • Target Background

    This gene encodes a vitamin K-dependent plasma glycoprotein. The encoded protein is cleaved to its activated form by the thrombin-thrombomodulin complex. This activated form contains a serine protease domain and functions in degradation of the activated forms of coagulation factors V and VIII. Mutations in this gene have been associated with thrombophilia due to protein C deficiency, neonatal purpura fulminans, and recurrent venous thrombosis.

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