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Cow (Bovine) Polyclonal GOT2 Primary Antibody for WB - ABIN2781299
Tsai, Hong, Liou, Liao: Association study of GOT2 genetic polymorphisms and schizophrenia. in Psychiatric genetics 2007
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Human Monoclonal GOT2 Primary Antibody for ICC, ELISA - ABIN1724722
Zhou, Gordon, Bradbury, Stump, Kiang, Berk: Ethanol up-regulates fatty acid uptake and plasma membrane expression and export of mitochondrial aspartate aminotransferase in HepG2 cells. in Hepatology (Baltimore, Md.) 1998
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Human Polyclonal GOT2 Primary Antibody for ELISA, WB - ABIN561090
Orr, Li, Wang, Li, Wang, Rong, Xu, Mastroberardino, Greenamyre, Li: N-terminal mutant huntingtin associates with mitochondria and impairs mitochondrial trafficking. in The Journal of neuroscience : the official journal of the Society for Neuroscience 2008
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Cow (Bovine) Polyclonal GOT2 Primary Antibody for IHC, WB - ABIN2781301
Suzuki, Yoshitomo-Nakagawa, Maruyama, Suyama, Sugano: Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. in Gene 1997
Human Polyclonal GOT2 Primary Antibody for ELISA, WB - ABIN4315403
Teichberg: From the liver to the brain across the blood-brain barrier. in Proceedings of the National Academy of Sciences of the United States of America 2007
Thermal aggregation of aspartate aminotransferase from pig heart mitochondria (mAAT) has been studied at various temperatures and various protein concentrations by dynamic light scattering.
it is quite likely that the down regulation of GOT2 after blast exposure is playing a significant role in mitochondrial dysfunction after blast exposure
The role of mAspAT in vivo is to control the levels of endogenous kynurenic acid (KYNA) through modulation of the mAspAt in the mouse brain.
KAT IV inhibited by equimolar tryptophan and aspartate, and half-life is 6.5 minutes at 65 degree C.
FAT/CD36 (show CD36 Antibodies) and FABPpm protein content was increased in red muscles in IL-6 (show IL6 Antibodies)(-/-) mice compared to WT mice at 4 (RG) and 12 months (soleus and RG).
sialin possesses dual physiological functions and acts as a vesicular aspartate/glutamate transporter (show SLC1A1 Antibodies)
Like in adults, FABP (show FABP2 Antibodies) seems to be associated with markers of metabolic risk in obese adolescents
Elevated levels of AST are Associated with Cardiovascular disease.
Data suggest that, in context of abnormal hepatic lipid accumulation in nonalcoholic fatty liver disease, circulating GOT2 rises due to up-regulation of hepatic expression of GOT2 associated with greater gluconeogenesis and insulin (show INS Antibodies) resistance.
A previously unknown mechanism by which GOT2 acetylation stimulates the malate-aspartate NADH shuttle activity and oxidative protection.
The lipid binding process in L-FABP is associated with backbone dynamics.
This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form.
proton-coupled sialic acid transporter
, solute carrier family 17 (anion/sugar transporter), member 5
, membrane glycoprotein SP55
, sodium/sialic acid cotransporter
, solute carrier family 17 member 5
, aspartate aminotransferase, mitochondrial
, glutamate oxaloacetate transaminase 2
, glutamic-oxaloacetic transaminase 2, mitochondrial (aspartate aminotransferase 2)
, kynurenine aminotransferase 4
, kynurenine aminotransferase IV
, kynurenine--oxoglutarate transaminase 4
, kynurenine--oxoglutarate transaminase IV
, transaminase A
, fatty acid-binding protein
, plasma membrane-associated fatty acid-binding protein
, mitochondrial aspartate aminotransferase
, plasma membrane fatty acid binding protein
, aspartate aminotransferase 2
, aspartate transaminase 2
, Glutamate oxaloacetate transaminase 2, mitochondrial (aspartate aminotransferase 2)
, aspartate aminotransferase 2a
, H(+)/nitrate cotransporter
, H(+)/sialic acid cotransporter
, membrane glycoprotein HP59
, sialic acid storage disease
, solute carrier family 17, member 5
, vesicular H(+)/Aspartate-glutamate cotransporter