-
Product Name
GGCX antibody
- Documents
-
Description
GGCX Rabbit Polyclonal antibody. Positive IHC detected in human liver tissue, human brain tissue. Positive WB detected in MCF7 cells, HEK-293 cells, HepG2 cells, L02 cells, mouse liver tissue, PC-3 cells. Positive IP detected in mouse liver tissue. Observed molecular weight by Western-blot: 88 kDa
-
Tested applications
ELISA, WB, IHC, IP
-
Species reactivity
Human,Mouse,Rat; other species not tested.
-
Alternative names
FLJ26629 antibody; gamma glutamyl carboxylase antibody; GGCX antibody; VKCFD1 antibody
-
Isotype
Rabbit IgG
-
Preparation
This antibody was obtained by immunization of GGCX recombinant protein (Accession Number: NM_000821). Purification method: Antigen affinity purified.
-
Clonality
Polyclonal
-
Formulation
PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
-
Storage instructions
Store at -20℃. DO NOT ALIQUOT
-
Applications
Recommended Dilution:
WB: 1:1000-1:10000
IP: 1:1000-1:10000
IHC: 1:20-1:200
-
Validations
MCF7 cells were subjected to SDS PAGE followed by western blot with Catalog No:110959(GGCX antibody) at dilution of 1:2000
Immunohistochemical of paraffin-embedded human liver using Catalog No:110959(GGCX antibody) at dilution of 1:100 (under 10x lens)
Immunohistochemical of paraffin-embedded human liver using Catalog No:110959(GGCX antibody) at dilution of 1:100 (under 40x lens)
IP Result of anti-GGCX (IP:Catalog No:110959, 4ug; Detection:Catalog No:110959 1:2000) with mouse liver tissue lysate 4000ug.
-
Background
GGCX(Gamma-glutamyl carboxylase) is also named as GC and belongs to the vitamin K-dependent gamma-carboxylase family. This 94 kDa (including all modifications, such as the five N-linked glycosylations), is a 5-pass transmembrane protein and a key regulator of blood coagulation(PMID:20518534). It mediates the vitamin K-dependent carboxylation of glutamate residues to calcium-binding gamma-carboxyglutamate (Gla) residues with the concomitant conversion of the reduced hydroquinone form of vitamin K to vitamin K epoxide. Defects in GGCX are a cause of combined deficiency of vitamin K-dependent clotting factors type 1 (VKCFD1) and pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency (PXEL-MCFD)(PMID:9845520;17110937).
-
References
- Ferron M, Lacombe J, Germain A, Oury F, Karsenty G. GGCX and VKORC1 inhibit osteocalcin endocrine functions. The Journal of cell biology. 208(6):761-76. 2015.
Related Products / Services
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"