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Aluminum+oxide-Silicon+oxide
Artikel-Nr:
(BOSSBS-6716R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6716R-FITC
Lokale Artikelnummer::
BOSSBS-6716R-FITC
Beschreibung:
Uricase catalyzes the oxidation of uric acid to 5 hydroxyisourate which spontaneously decomposes to form allantoin.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11997R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11997R
Lokale Artikelnummer::
BOSSBS-11997R
Beschreibung:
DDAH, a dimethylarginine dimethylaminohydrolase, hydrolyzes dimethyl arginine (ADMA) and monomethyl arginine (MMA), both inhibitors of nitric oxide synthases, and may be involved in in-vivo modulation of nitric oxide production (1,2). Impairment of DDAH causes ADMA accumulation and a reduction in cGMP generation (3). DDAH II, the predominant DDAH isoform in endothelial cells, facilitates the induction of nitric oxide synthesis by all-trans-Retinoic acid (atRA) (4). DDAH proteins are highly expressed in colon, kidney, stomach and liver tissues (1).
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
Pure Al₂O₃<sub> </sub>Aluminium oxide, AL25.
Artikel-Nr:
(BOSSBS-5018R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5018R-CY3
Lokale Artikelnummer::
BOSSBS-5018R-CY3
Beschreibung:
ACADVL (acyl-Coenzyme A dehydrogenase, very long chain) catalyzes the first step of the mitochondrial fatty acid beta-oxidation pathway. It is specific to esters of long-chain and very long chain fatty acids such as palmitoyl-CoA and stearoyl-CoA. Deficiencies in ACADVL are associated with reduced myocardial fatty acid beta-oxidation and cardiomyopathy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5018R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5018R-CY5
Lokale Artikelnummer::
BOSSBS-5018R-CY5
Beschreibung:
ACADVL (acyl-Coenzyme A dehydrogenase, very long chain) catalyzes the first step of the mitochondrial fatty acid beta-oxidation pathway. It is specific to esters of long-chain and very long chain fatty acids such as palmitoyl-CoA and stearoyl-CoA. Deficiencies in ACADVL are associated with reduced myocardial fatty acid beta-oxidation and cardiomyopathy.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
Cobalt(II)wolframat ≥99%
Artikel-Nr:
(BOSSBS-5048R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5048R-A750
Lokale Artikelnummer::
BOSSBS-5048R-A750
Beschreibung:
Beta-oxidation of fatty acids. The highest activity concerns the C6 to C10 chain length substrate. Converts the end product of pristanic acid beta oxidation, 4,8-dimethylnonanoyl-CoA, to its corresponding carnitine ester.
VE:
1 * 100 µl
Artikel-Nr:
(WILMBMS-005B)
Lieferant:
WILMAD LAB GLASS LUREX
Hersteller-Artikelnummer::
BMS-005B
Lokale Artikelnummer::
WILMBMS-005B
Beschreibung:
Susceptibility matched tubes can reduce the sample volume down to 1/3 by minimising the susceptibility gradients occurring at the solvent-air interface.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-8329R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8329R-CY7
Lokale Artikelnummer::
BOSSBS-8329R-CY7
Beschreibung:
Contributes to oxidative stress resistance by reducing cysteine-sulfinic acid formed under exposure to oxidants in the peroxiredoxins PRDX1, PRDX2, PRDX3 and PRDX4. Does not act on PRDX5 or PRDX6. May catalyze the reduction in a multi-step process by acting both as a specific phosphotransferase and a thioltransferase.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-(Chlormethyl)-2-ethyloxiran 95%
Artikel-Nr:
(BOSSBS-6313R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6313R-CY5
Lokale Artikelnummer::
BOSSBS-6313R-CY5
Beschreibung:
Aldehydic products of lipid peroxidation, such as 4 hydroxynonenal (4 HNE), have been implicated in the etiology of pathological changes under oxidative stress as a key mediator of oxidative stress induced cell death. It is a stable product of lipid peroxidation, is proarrhythmic and may contribute to the cytotoxic effects of oxidative stress
4-HNE has been hypothesized to play a key role in cell signal transduction, in a variety of pathways from cell cycle events to cellular adhesion.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5018R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5018R-A680
Lokale Artikelnummer::
BOSSBS-5018R-A680
Beschreibung:
ACADVL (acyl-Coenzyme A dehydrogenase, very long chain) catalyses the first step of the mitochondrial fatty acid beta-oxidation pathway. It is specific to esters of long-chain and very long chain fatty acids such as palmitoyl-CoA and stearoyl-CoA. Deficiencies in ACADVL are associated with reduced myocardial fatty acid beta-oxidation and cardiomyopathy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5048R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5048R-HRP
Lokale Artikelnummer::
BOSSBS-5048R-HRP
Beschreibung:
Beta-oxidation of fatty acids. The highest activity concerns the C6 to C10 chain length substrate. Converts the end product of pristanic acid beta oxidation, 4,8-dimethylnonanoyl-CoA, to its corresponding carnitine ester.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13186R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13186R-HRP
Lokale Artikelnummer::
BOSSBS-13186R-HRP
Beschreibung:
The Flavin containing monooxygenase family consists of five gene products, FMO1-5, that are major enzymatic oxidants involved in the metabolism of various therapeutics. Located in the liver, FMO3 is a hepatic microsomal enzyme that oxygenates soft nucleophiles such as secondary and tertiary amines. Through its N-oxygenase capabilities, FMO3 acts on a variety of xenobiotics to catalyze oxidative digestion. Defects in the FMO3 gene are the primary cause of trimethylaminuria (TMAuria), an inborn error of metabolism associated with a fishy body odor emitting from sweat, urine and breath. Genetic mutations in FMO3 lead to the N-oxidation of amino-trimethylamine derived from food products, thus producing the malodor associated with TMAuria.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13186R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13186R-A680
Lokale Artikelnummer::
BOSSBS-13186R-A680
Beschreibung:
The Flavin containing monooxygenase family consists of five gene products, FMO1-5, that are major enzymatic oxidants involved in the metabolism of various therapeutics. Located in the liver, FMO3 is a hepatic microsomal enzyme that oxygenates soft nucleophiles such as secondary and tertiary amines. Through its N-oxygenase capabilities, FMO3 acts on a variety of xenobiotics to catalyze oxidative digestion. Defects in the FMO3 gene are the primary cause of trimethylaminuria (TMAuria), an inborn error of metabolism associated with a fishy body odor emitting from sweat, urine and breath. Genetic mutations in FMO3 lead to the N-oxidation of amino-trimethylamine derived from food products, thus producing the malodor associated with TMAuria.
VE:
1 * 100 µl
Lieferant:
Cayman Chemical
Beschreibung:
Propylphosphonic acid is a compound that is highly susceptible to degradation by radical species. It is used to investigate the inactivation of <i>A. hydrophila</i> by free radicals produced spontaneously in oxidizing iron-containing groundwaters and also to to identify toxic nerve agents in water samples.
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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