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MGP Monoclonal antibody, PBS Only (Capture)

MGP Monoclonal Antibody for WB, IHC, IF/ICC, IF-P, IF-Fro, Cytometric bead array, Indirect ELISA
Cat No. 60055-1-PBS
Clone No.1A1C3

Host / Isotype

Mouse / IgG2a

Reactivity

human, mouse

Applications

WB, IHC, IF/ICC, IF-P, IF-Fro, Cytometric bead array, Indirect ELISA

GIG36, 1A1C3, Cell growth-inhibiting gene 36 protein, matrix Gla protein, MGLAP

Formulation:  PBS Only
Conjugate:  Unconjugated
Size/Concentration: 

-/ -

Freight/Packing: -

Quantity

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Product Information

60055-1-PBS targets MGP as part of a matched antibody pair:

MP51512-1: 60055-1-PBS capture and 60055-2-PBS detection (validated in Cytometric bead array)

Unconjugated mouse monoclonal antibody pair in PBS only (BSA and azide free) storage buffer at a concentration of 1 mg/mL, ready for conjugation.

This conjugation ready format makes antibodies ideal for use in many applications including: ELISAs, multiplex assays requiring matched pairs, mass cytometry, and multiplex imaging applications.Antibody use should be optimized by the end user for each application and assay.

Tested Reactivity human, mouse
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Immunogen

CatNo: Ag1091

Product name: Recombinant human MGP protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 1-103 aa of BC005272

Sequence: MKSLILLAILAALAVVTLCYESHESMESYELNPFINRRNANTFISPQQRWRAKVQERIRERSKPVHELNREACDDYRLCERYAMVYGYNAAYNRYFRKRRGAK

Predict reactive species
Full Name matrix Gla protein
Calculated Molecular Weight 103 aa, 13 kDa
Observed Molecular Weight 12 kDa
GenBank Accession NumberBC005272
Gene Symbol MGP
Gene ID (NCBI) 4256
RRIDAB_2143330
Conjugate Unconjugated
FormLiquid
Purification MethodProtein A purification
UNIPROT IDP08493
Storage Buffer PBS only, pH 7.3.
Storage ConditionsStore at -80°C.

Background Information

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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