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Product Name
MGP antibody
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Description
MGP Mouse Monoclonal antibody. Positive IHC detected in human lung tissue, human brain tissue, human gliomas tissue. Positive WB detected in Transfected HEK-293 cells, human brain tissue, human kidney tissue. Observed molecular weight by Western-blot: 12 kDa
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Tested applications
ELISA, IHC, WB
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Species reactivity
Human, Mouse; other species not tested.
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Alternative names
GIG36 antibody; matrix Gla protein antibody; MGLAP antibody; MGP antibody; NTI antibody
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Isotype
Mouse IgG2a
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Preparation
This antibody was obtained by immunization of MGP recombinant protein (Accession Number: NM_000900). Purification method: Caprylic acid/ammonium sulfate precipitation.
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Clonality
Monoclonal
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Formulation
PBS with 0.1% sodium azide and 50% glycerol pH 7.3.
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Storage instructions
Store at -20℃. DO NOT ALIQUOT
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Applications
Recommended Dilution:
WB: 1:500-1:5000
IHC: 1:20-1:200
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Validations
Immunohistochemical of paraffin-embedded human lung using Catalog No:107425(MGP antibody) at dilution of 1:50 (under 10x lens)
Immunohistochemical of paraffin-embedded human lung using Catalog No:107425(MGP antibody) at dilution of 1:50 (under 40x lens)
Transfected HEK-293 cells were subjected to SDS PAGE followed by western blot with Catalog No:107425(MGP Antibody) at dilution of 1:1000
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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.
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