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The protein encoded by AGXT2 is a class III pyridoxal-phosphate-dependent mitochondrial aminotransferase. Additionally we are shipping Alanine Glyoxylate Aminotransferase 2 Kits (9) and Alanine Glyoxylate Aminotransferase 2 Proteins (5) and many more products for this protein.
Showing 10 out of 28 products:
Human Polyclonal AGXT2 Primary Antibody for WB - ABIN2783579
Baker, Cramer, Kennedy, Assimos, Holmes: Glycolate and glyoxylate metabolism in HepG2 cells. in American journal of physiology. Cell physiology 2004
Human Polyclonal AGXT2 Primary Antibody for EIA, FACS - ABIN950306
Rodionov, Murry, Vaulman, Stevens, Lentz: Human alanine-glyoxylate aminotransferase 2 lowers asymmetric dimethylarginine and protects from inhibition of nitric oxide production. in The Journal of biological chemistry 2010
Human Polyclonal AGXT2 Primary Antibody for ICC, IF - ABIN4278743
Kittel, Müller, König, Mieth, Sticht, Zolk, Kralj, Heinrich, Fromm, Maas: Alanine-glyoxylate aminotransferase 2 (AGXT2) polymorphisms have considerable impact on methylarginine and β-aminoisobutyrate metabolism in healthy volunteers. in PLoS ONE 2014
AGXT2 rs37369 polymorphism is associated with increased risk for CHD (show CHDH Antibodies) in smokers and in diabetes mellitus patients
The AGXT2 genotype may be an important factor underlying atherosclerosis.
The results of this study that the AGXT2 gene is not associated with schizophrenia in Japanese subjects.
SNPs of AGXT2 affect plasma as well as urinary BAIB.
AGXT2 has an important role in SDMA metabolism in humans and may additionally have an unanticipated role in the autonomic nervous system regulation of cardiac function.
Alanine-glyoxylate aminotransferase-2 metabolizes endogenous methylarginines, regulates NO, and controls blood pressure.
mitochondrially localized human AGXT2 is able to effectively metabolize ADMA in vivo resulting in decreased ADMA levels and improved endothelial NO production.
In this work, we describe an assay for the AGXT2 activity in mouse liver and kidney tissue. The overall production rates of DMGV-d(6) in mice were 195.37 pmol/min/mg total protein in liver and 85.21 pmol/min/mg total protein in kidney tissue.
The protein encoded by this gene is a class III pyridoxal-phosphate-dependent mitochondrial aminotransferase. It catalyzes the conversion of glyoxylate to glycine using L-alanine as the amino donor.
, alanine--glyoxylate aminotransferase 2, mitochondrial
, beta-ALAAT II
, beta-alanine-pyruvate aminotransferase
, AGT 2
, alanine-glyoxylate aminotransferase 2