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MGP antibody

The Rabbit Polyclonal anti-MGP antibody has been validated for IHC and ELISA. It is suitable to detect MGP in samples from Human, Rat and Mouse.
Catalog No. ABIN7246430

Quick Overview for MGP antibody (ABIN7246430)

Target

See all MGP Antibodies
MGP (Matrix Gla Protein (MGP))

Reactivity

  • 26
  • 23
  • 16
  • 3
  • 3
  • 3
  • 1
  • 1
Human, Rat, Mouse

Host

  • 48
  • 6
  • 3
  • 1
Rabbit

Clonality

  • 54
  • 4
Polyclonal

Conjugate

  • 34
  • 10
  • 6
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MGP antibody is un-conjugated

Application

  • 47
  • 37
  • 25
  • 20
  • 8
  • 4
  • 3
  • 3
  • 2
  • 1
Immunohistochemistry (IHC), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Fusion protein of human MGP

    Isotype

    IgG
  • Application Notes

    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

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    MGP (Matrix Gla Protein (MGP))

    Alternative Name

    MGP

    Background

    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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