Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
Weitere Synonyme anzeigen
Wählen Sie die gewünschte Spezies
The results of our study on this larger than 5800-patient cohort suggest beneficial effects of high B12 vitamin level, negative effects of high sodium levels or high AST (aspartate aminotransferase) liver enzyme levels to cognition.
Like in adults, FABP (zeige FABP2 Proteine) 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 (zeige INS Proteine) 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.
Thermal aggregation of aspartate aminotransferase from pig heart mitochondria (mAAT) has been studied at various temperatures and various protein concentrations by dynamic light scattering.
GOT2-mediated ATP synthesis may be a pivotal mechanism underlying the protective effect of febuxostat against neurodegeneration in EA
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 (zeige NEK1 Proteine) IV inhibited by equimolar tryptophan and aspartate, and half-life is 6.5 minutes at 65 degree C.
FAT/CD36 (zeige CD36 Proteine) and FABPpm protein content was increased in red muscles in IL-6 (zeige IL6 Proteine)(-/-) mice compared to WT mice at 4 (RG) and 12 months (soleus and RG).
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.
, aspartate aminotransferase 2
, aspartate aminotransferase, mitochondrial
, aspartate transaminase 2
, fatty acid-binding protein
, 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
, plasma membrane-associated fatty acid-binding protein
, transaminase A
, H(+)/nitrate cotransporter
, H(+)/sialic acid cotransporter
, membrane glycoprotein HP59
, sialic acid storage disease
, sodium/sialic acid cotransporter
, solute carrier family 17 (anion/sugar transporter), member 5
, solute carrier family 17 member 5
, solute carrier family 17, member 5
, vesicular H(+)/Aspartate-glutamate cotransporter
, mitochondrial aspartate aminotransferase
, plasma membrane fatty acid binding protein
, Glutamate oxaloacetate transaminase 2, mitochondrial (aspartate aminotransferase 2)
, aspartate aminotransferase 2a
, glutamate oxaloacetate transaminase 2, mitochondrial