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Merck

A2903

Sigma-Aldrich

Acyl Coenzyme A Oxidase from Candida sp.

lyophilized powder, 10-30 units/mg protein

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About This Item

Número de CAS:
Comisión internacional de enzimas:
Número MDL:
Código UNSPSC:
12352204
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Formulario

lyophilized powder

actividad específica

10-30 units/mg protein

temp. de almacenamiento

−20°C

Definición de unidad

One unit will form 1.0 μmole of H2O2 and hexadecenoyl-CoA from palmitoyl-CoA per min at pH 8.0 at 30 °C in a peroxidase coupled system.

Forma física

Contains sucrose as stabilizer; protein determined by biuret

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Eriko Misawa et al.
Journal of agricultural and food chemistry, 60(11), 2799-2806 (2012-02-23)
We investigated the effects of the oral administration of lophenol (Lo) and cycloartanol (Cy), two kinds of antidiabetic phytosterol isolated from Aloe vera , on glucose and lipid metabolism in Zucker diabetic fatty (ZDF) rats. We demonstrated that the administrations
Elin Strand et al.
Lipids in health and disease, 11, 82-82 (2012-06-29)
Excess peroxisome proliferator-activated receptor (PPAR) stimulation has been associated with detrimental health effects including impaired myocardial function. Recently, supplementation with n-3 polyunsaturated fatty acids (PUFA) has been associated with improved left ventricular function and functional capacity in patients with dilated
Daniel González-Mañán et al.
Food & function, 3(7), 765-772 (2012-05-17)
High dietary intake of n-6 fatty acids in relation to n-3 fatty acids may generate health disorders, such as cardiovascular and other chronic diseases. Fish consumption rich in n-3 fatty acids is low in Latin America, it being necessary to
Federico Salamone et al.
World journal of gastroenterology, 18(29), 3862-3868 (2012-08-10)
To establish if the juice of Moro, an anthocyanin-rich orange, may improve liver damage in mice with diet-induced obesity. Eight-week-old mice were fed a high-fat diet (HFD) and were administrated water or Moro juice for 12 wk. Liver morphology, gene
Myriam Baes et al.
Biochimica et biophysica acta, 1822(9), 1489-1500 (2012-03-27)
Peroxisome biogenesis and peroxisomal β-oxidation defects are rare inherited metabolic disorders in which several organs can be affected. A panel of mouse models has been created in which genes crucial to these processes were inactivated and the ensuing pathologies studied.

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