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MGP Protein (His tag)

MGP Origin: Human Host: Escherichia coli (E. coli) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2725556
  • Target See all MGP Proteins
    MGP (Matrix Gla Protein (MGP))
    Protein Type
    Recombinant
    Origin
    • 4
    • 4
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Source
    • 13
    • 8
    • 1
    Escherichia coli (E. coli)
    Purification tag / Conjugate
    This MGP protein is labelled with His tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human Matrix Gla Protein (full length, N-term HIS tag, transcript variant 2) protein expressed in E. coli.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product MGP Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    The tag is located at the N-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.
    Storage
    -80 °C
    Storage Comment
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target
    MGP (Matrix Gla Protein (MGP))
    Alternative Name
    Matrix Gla Protein (MGP Products)
    Synonyms
    MGLAP Protein, NTI Protein, Mglap Protein, mgp-A Protein, MGP Protein, LOC100136434 Protein, mgp Protein, matrix Gla protein Protein, matrix Gla protein L homeolog Protein, MGP Protein, Mgp Protein, mgp.L Protein, mgp Protein
    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.
    Molecular Weight
    12.2 kDa
    NCBI Accession
    NP_000891
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