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Recombinant Human Metalloproteinase inhibitor 2 protein (TIMP2)

ACP24709

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Main Attributes


Cat.No ACP24709 Target NameTIMP2
FormLiquid or Lyophilized powderExpression SystemE.coli
Mol Weight21.8 kDaPurity>85% as determined by SDS-PAGE and HPLC.
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.

Others Attributes


Target SpeciesHumanUniprot IDP16035
Background Information
  • Uniprot Id

    P16035

  • Target Species

    Human

  • Target Name

    TIMP2

  • Target Full Name

    Metalloproteinase inhibitor 2

  • Target Function

    Complexes with metalloproteinases (such as collagenases) and irreversibly inactivates them by binding to their catalytic zinc cofactor. Known to act on MMP-1, MMP-2, MMP-3, MMP-7, MMP-8, MMP-9, MMP-10, MMP-13, MMP-14, MMP-15, MMP-16 and MMP-19.

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    Protease inhibitor I35 (TIMP) family

  • Target Research Area

    Cardiovascular

  • Target Synonyms

    CSC 21K; CSC-21K; CSC21K; Metalloproteinase inhibitor 2; Metalloproteinase inhibitor 2 precursor; TIMP 2; TIMP metallopeptidase inhibitor 2; TIMP-2; TIMP2; TIMP2_HUMAN; Tissue Inhibitor of Metalloproteinase 2; Tissue inhibitor of metalloproteinases 2

  • Target Background

    This gene is a member of the TIMP gene family. The proteins encoded by this gene family are natural inhibitors of the matrix metalloproteinases, a group of peptidases involved in degradation of the extracellular matrix. In addition to an inhibitory role against metalloproteinases, the encoded protein has a unique role among TIMP family members in its ability to directly suppress the proliferation of endothelial cells. As a result, the encoded protein may be critical to the maintenance of tissue homeostasis by suppressing the proliferation of quiescent tissues in response to angiogenic factors, and by inhibiting protease activity in tissues undergoing remodelling of the extracellular matrix.

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