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Microsomal arylacetamide deacetylase competes against the activity of cytosolic arylamine N-acetyltransferase, which catalyzes one of the initial biotransformation pathways for arylamine and heterocyclic amine carcinogens [provided by RefSeq, Jul 2008].. Zusätzlich bieten wir Ihnen Arylacetamide Deacetylase (Esterase) Proteine (11) und viele weitere Produktgruppen zu diesem Protein an.
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Human Monoclonal AADAC Primary Antibody für ELISA, WB - ABIN513029
Watanabe, Fukami, Nakajima, Takamiya, Aoki, Yokoi: Human arylacetamide deacetylase is a principal enzyme in flutamide hydrolysis. in Drug metabolism and disposition: the biological fate of chemicals 2009
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Data suggest that metabolism (and possibly pharmacokinetics) of hypnotic nitrazepam involves liver enzymes AOX1 (aldehyde oxidase 1 (zeige AOX1 Antikörper)), NAT2 (N-acetyltransferase 2 (zeige NAT2 Antikörper)), AADAC (arylacetamide deacetylase), and CYP3A4 (cytochrome P450 3A4 (zeige CYP3A4 Antikörper)).
Data suggest that AADAC in hepatocyte microsomes hydrolyzes ketoconazole, a synthetic imidazole antifungal agent, to N-deacetyl ketoconazole and thus triggers hepatocellular toxicity.
AADAC deletion is a candidate susceptibility factor for Gilles de la Tourette Syndrome
Translational N-glycosylation of AADAC plays a crucial role in regulating AADAC enzyme activity.
Lipolysis of cellular TG and VLDL production were impaired in HCV infected cells during the early peak of viral infection. This was partially explained by an apparent deficiency of a putative TG lipase (zeige LIPG Antikörper), arylacetamide deacetylase (AADAC).
An AADAC*3 allele yields decreased enzyme activity in liver microsomes.
human AADAC was the enzyme responsible for the deacetylation of rifamycins and would affect the induction rate of drug-metabolizing enzymes by rifamycins and their induced hepatotoxicity.
two intrinsic endoplasmic reticulum (ER) proteins, 11beta-hydroxysteroid dehydrogenase, isozyme 1 (11beta-HSD (zeige CHST3 Antikörper)) and the 50-kDa esterase (zeige ESD Antikörper) (E3), sharing some amino acid sequence motifs in their N-terminal transmembrane (TM) domains.
Expression of AADA cDNA in McArdle-RH7777 cells significantly reduced intracellular triacylglycerol levels and apolipoprotein B (zeige APOB Antikörper) secretion and increased fatty acid oxidation.
Microsomal arylacetamide deacetylase competes against the activity of cytosolic arylamine N-acetyltransferase, which catalyzes one of the initial biotransformation pathways for arylamine and heterocyclic amine carcinogens
arylacetamide deacetylase (esterase)
, arylacetamide deacetylase-like
, Arylacetamide deacetylase
, arylacetamide deacetylase
, arylacetamide deacetylase-like 2