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Recombinant Human Matrix Gla protein (MGP)

ACP02032

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP02032 Target NameMGP
Target SynonymsCell growth inhibiting gene 36 protein; Cell growth-inhibiting gene 36 protein; GAMMA-CARBOXYGLUTAMIC ACID PROTEIN, MATRIX; GIG36; Matrix Gla protein; MGLAP; MGP; MGP_HUMAN; NTIFormLiquid or Lyophilized powder
Expression SystemE.coliExpression Range20-96aa
Mol Weight14.5 kDaProtein LengthFull Length of Mature Protein
PurityGreater than 90% 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 IDP08493
Background Information
  • Uniprot Id

    P08493

  • Target Species

    Human

  • Target Name

    MGP

  • Target Full Name

    Matrix Gla protein

  • Target Function

    Associates with the organic matrix of bone and cartilage. Thought to act as an inhibitor of bone formation.

  • Target Involvement

    Keutel syndrome (KTLS)

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    Osteocalcin/matrix Gla protein family

  • Target Research Area

    Developmental Biology, Signal Transduction

  • Target Synonyms

    Cell growth inhibiting gene 36 protein; Cell growth-inhibiting gene 36 protein; GAMMA-CARBOXYGLUTAMIC ACID PROTEIN, MATRIX; GIG36; Matrix Gla protein; MGLAP; MGP; MGP_HUMAN; NTI

  • Target Background

    This gene encodes a member of the osteocalcin/matrix Gla family of proteins. The encoded vitamin K-dependent protein is secreted by chondrocytes and vascular smooth muscle cells, and functions as a physiological inhibitor of ectopic tissue calcification. Carboxylation status of the encoded protein is associated with calcification of the vasculature in human patients with cardiovascular disease and calcification of the synovial membranes in osteoarthritis patients. Mutations in this gene cause Keutel syndrome in human patients, which is characterized by abnormal cartilage calcification, peripheral pulmonary stenosis and facial hypoplasia.

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