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MGP anticorps

MGP Reactivité: Humain, Rat, Souris IHC, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7246430
  • Antigène Voir toutes MGP Anticorps
    MGP (Matrix Gla Protein (MGP))
    Reactivité
    • 23
    • 17
    • 13
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain, Rat, Souris
    Hôte
    • 33
    • 6
    • 2
    • 1
    Lapin
    Clonalité
    • 38
    • 4
    Polyclonal
    Conjugué
    • 22
    • 8
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp MGP est non-conjugé
    Application
    • 31
    • 19
    • 9
    • 7
    • 4
    • 4
    • 4
    • 2
    • 1
    • 1
    Immunohistochemistry (IHC), ELISA
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of human MGP
    Isotype
    IgG
    Top Product
    Discover our top product MGP Anticorps primaire
  • Indications d'application
    IHC 1:70-1:350, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.32 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    MGP (Matrix Gla Protein (MGP))
    Autre désignation
    MGP (MGP Produits)
    Sujet
    Matrix Gla protein (MGP) is is a vitamin K-dependent,extracellular matrix protein. MGP plays a pivotal role in preventing soft tissue calcification and local mineralization of the vascular wall. Vitamin K deficiency leads to inactive uncarboxylated MGP (ucMGP),which accumulates at sites of arterial calcification. However MGP is synthesized in many tissues and is especially enriched in embryonic tissues and in cancer cells. Defects in MGP are the cause of Keutel syndrome (KS),which is an autosomal recessive disorder characterized by abnormal cartilage calcification,peripheral pulmonary stenosis neural hearing loss and midfacial hypoplasia.
    UniProt
    P08493
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