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3M+Food+Safety
Artikel-Nr:
(BOSSBS-13459R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13459R-CY3
Lokale Artikelnummer::
BOSSBS-13459R-CY3
Beschreibung:
In the de novo synthesis of purine nucleotides, IMP is the branch point metabolite at which point the pathway diverges to the synthesis of either guanine or adenine nucleotides. In the guanine nucleotide pathway, there are 2 enzymes involved in converting IMP to GMP, namely IMP dehydrogenase (IMPD1), which catalyzes the oxidation of IMP to XMP, and GMP synthetase, which catalyzes the amination of XMP to GMP. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10150R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10150R-A750
Lokale Artikelnummer::
BOSSBS-10150R-A750
Beschreibung:
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyse the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13459R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13459R-A488
Lokale Artikelnummer::
BOSSBS-13459R-A488
Beschreibung:
In the de novo synthesis of purine nucleotides, IMP is the branch point metabolite at which point the pathway diverges to the synthesis of either guanine or adenine nucleotides. In the guanine nucleotide pathway, there are 2 enzymes involved in converting IMP to GMP, namely IMP dehydrogenase (IMPD1), which catalyzes the oxidation of IMP to XMP, and GMP synthetase, which catalyzes the amination of XMP to GMP. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5015R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5015R-A680
Lokale Artikelnummer::
BOSSBS-5015R-A680
Beschreibung:
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyse the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13459R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13459R-A647
Lokale Artikelnummer::
BOSSBS-13459R-A647
Beschreibung:
In the de novo synthesis of purine nucleotides, IMP is the branch point metabolite at which point the pathway diverges to the synthesis of either guanine or adenine nucleotides. In the guanine nucleotide pathway, there are 2 enzymes involved in converting IMP to GMP, namely IMP dehydrogenase (IMPD1), which catalyzes the oxidation of IMP to XMP, and GMP synthetase, which catalyzes the amination of XMP to GMP. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(APOSPC905429-250MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC905429-250MG
Lokale Artikelnummer::
APOSPC905429-250MG
Beschreibung:
6-(Trifluoromethyl)imidazo[1,2-a]pyridin-2-amine 95%
VE:
1 * 250 mg
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-Aminomethyl-2-(boc-amino)pyridine 95%
Artikel-Nr:
(BOSSBS-1859R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1859R-A680
Lokale Artikelnummer::
BOSSBS-1859R-A680
Beschreibung:
Involved in oxygen transport in the brain. Hexacoordinate globin, displaying competitive binding of oxygen or the distal His residue to the iron atom. Not capable of penetrating cell membranes. The deoxygenated form exhibits nitrite reductase activity inhibiting cellular respiration via NO-binding to cytochrome c oxidase. Involved in neuroprotection during oxidative stress. May exert its anti-apoptotic activity by acting to reset the trigger level of mitochondrial cytochrome c release necessary to commit the cells to apoptosis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1859R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1859R-A750
Lokale Artikelnummer::
BOSSBS-1859R-A750
Beschreibung:
Involved in oxygen transport in the brain. Hexacoordinate globin, displaying competitive binding of oxygen or the distal His residue to the iron atom. Not capable of penetrating cell membranes. The deoxygenated form exhibits nitrite reductase activity inhibiting cellular respiration via NO-binding to cytochrome c oxidase. Involved in neuroprotection during oxidative stress. May exert its anti-apoptotic activity by acting to reset the trigger level of mitochondrial cytochrome c release necessary to commit the cells to apoptosis.
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR345529-250MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR345529-250MG
Lokale Artikelnummer::
APOSOR345529-250MG
Beschreibung:
3-Bromo-5-(prop-1-en-2-yl)pyridine 95+%
VE:
1 * 250 mg
Artikel-Nr:
(BOSSBS-10150R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10150R-CY5
Lokale Artikelnummer::
BOSSBS-10150R-CY5
Beschreibung:
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5015R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5015R-CY5.5
Lokale Artikelnummer::
BOSSBS-5015R-CY5.5
Beschreibung:
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10150R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10150R-CY7
Lokale Artikelnummer::
BOSSBS-10150R-CY7
Beschreibung:
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6365R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6365R
Lokale Artikelnummer::
BOSSBS-6365R
Beschreibung:
This gene encodes a member of the carnitine/choline acetyltransferase family. The encoded protein converts 4,8-dimethylnonanoyl-CoA to its corresponding carnitine ester. This transesterification occurs in the peroxisome and is necessary for transport of medium- and long- chain acyl-CoA molecules out of the peroxisome to the cytosol and mitochondria. The protein thus plays a role in lipid metabolism and fatty acid beta-oxidation. Alternatively spliced transcript variants have been described.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2,3-Dichlor-5-(trichlormethyl)pyridin
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-Brom-2-methylimidazo[1,2-a]pyridin
Preis auf Anfrage
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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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