A4326
Arylamine acetyltransferase from pigeon liver
lyophilized powder, ~0.5 units/mg protein
Sinonimo/i:
NAT
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About This Item
Numero CAS:
Numero MDL:
Codice UNSPSC:
12352204
Prezzi e disponibilità al momento non sono disponibili
Origine biologica
pigeon liver
Stato
lyophilized powder
Attività specifica
~0.5 units/mg protein
Composizione
Protein, ~10% biuret
Condizioni di spedizione
dry ice
Temperatura di conservazione
−20°C
Definizione di unità
One unit will acetylate 1.0 nanomole of p-nitroaniline per min at pH 8.0 at 25 °C.
Stato fisico
Contains sucrose as a stabilizer.
Codice della classe di stoccaggio
13 - Non Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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Emanuel Roth et al.
Journal of toxicology and environmental health. Part A, 75(19-20), 1216-1225 (2012-09-22)
Long-term follow-ups on bladder cancer patients from highly industrialized areas are rare. Therefore, we present a follow-up of bladder cancer patients from the greater area Lutherstadt Wittenberg, a center of the chemical industry of the former German Democratic Republic. Relapse-free
Mariola Rychlik-Sych et al.
Przeglad lekarski, 69(3), 120-124 (2012-07-07)
The etiology of dermatological diseases is still unknown. Involvement of genetic and environmental factors in the pathogenesis of dermatological diseases has contributed to a number of studies whose aim is to elucidate the way in which xenobiotics exert effects on
Edith Sim et al.
Advances in pharmacology (San Diego, Calif.), 63, 169-205 (2012-07-11)
Arylamine N-acetyltransferases (NATs) are defined as xenobiotic metabolizing enzymes, adding an acetyl group from acetyl coenzyme A (CoA) to arylamines and arylhydrazines. NATs are found in organisms from bacteria and fungi to vertebrates. Several isoenzymes, often polymorphic, may be present
Maiyen Tran Hawkins et al.
Expert opinion on drug metabolism & toxicology, 8(12), 1521-1530 (2012-09-25)
The quest for a biomarker that would reliably identify patients at risk of developing acute drug-induced liver injury (DILI) to a specific agent or class of agents before it occurs, has been underway for years. Historical host factors for DILI
Francisco Jose Forestiero et al.
Clinica chimica acta; international journal of clinical chemistry, 415, 215-219 (2012-10-27)
The relationship of NAT2, CYP2E1 and GSTM1/GSTT1 polymorphisms with mild elevation of liver biomarkers was investigated in individuals under anti-tuberculosis drug therapy. Tuberculosis outpatients (18-70 y) with (n=59) and without (n=40) mild increase of liver enzymes (MILE) at two-month treatment
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