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Methyl+2,3-diamino-6-fluorobenzoate
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Methyl+2,3-diamino-6-fluorobenzoate
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-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:
(APOSBIA1796-100G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
BIA1796-100G
Lokale Artikelnummer::
APOSBIA1796-100G
Beschreibung:
(S)-2-Acetamido-3-methylbutanoic acid
VE:
1 * 100 g
Artikel-Nr:
(BOSSBS-5023R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5023R-CY5
Lokale Artikelnummer::
BOSSBS-5023R-CY5
Beschreibung:
AGPAT1 converts lysophosphatidic acid (LPA) into phosphatidic acid by incorporating an acyl moiety at the sn-2 position of the glycerol backbone.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5023R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5023R-CY3
Lokale Artikelnummer::
BOSSBS-5023R-CY3
Beschreibung:
AGPAT1 converts lysophosphatidic acid (LPA) into phosphatidic acid by incorporating an acyl moiety at the sn-2 position of the glycerol backbone.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5119R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5119R
Lokale Artikelnummer::
BOSSBS-5119R
Beschreibung:
This gene encodes a fatty acid amide hydrolase that shares a conserved protein motif with the amidase signature family of enzymes. The encoded enzyme is able to catalyze the hydrolysis of a broad range of bioactive lipids, including those from the three main classes of fatty acid amides; N-acylethanolamines, fatty acid primary amides and N-acyl amino acids. This enzyme has a preference for monounsaturated acyl chains as a substrate.[provided by RefSeq, Sep 2009]
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5015R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5015R-CY5
Lokale Artikelnummer::
BOSSBS-5015R-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-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5015R-A488
Lokale Artikelnummer::
BOSSBS-5015R-A488
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-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10150R-HRP
Lokale Artikelnummer::
BOSSBS-10150R-HRP
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-5033R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5033R-CY5
Lokale Artikelnummer::
BOSSBS-5033R-CY5
Beschreibung:
Converts lysophosphatidic acid (LPA) into phosphatidic acid by incorporating an acyl moiety at the sn-2 position of the glycerol backbone.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1924R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1924R-CY3
Lokale Artikelnummer::
BOSSBS-1924R-CY3
Beschreibung:
AGPAT6 is a novel glycerolipid acyltransferase of the ER, which is crucial for the production of milk fat by the mammary gland. It converts lysophosphatidic acid (LPA) into phosphatidic acid by incorporating an acyl moiety at the sn-2 position of the glycerol backbone.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5119R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5119R-CY5
Lokale Artikelnummer::
BOSSBS-5119R-CY5
Beschreibung:
This gene encodes a fatty acid amide hydrolase that shares a conserved protein motif with the amidase signature family of enzymes. The encoded enzyme is able to catalyze the hydrolysis of a broad range of bioactive lipids, including those from the three main classes of fatty acid amides; N-acylethanolamines, fatty acid primary amides and N-acyl amino acids. This enzyme has a preference for monounsaturated acyl chains as a substrate.[provided by RefSeq, Sep 2009]
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5119R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5119R-A488
Lokale Artikelnummer::
BOSSBS-5119R-A488
Beschreibung:
This gene encodes a fatty acid amide hydrolase that shares a conserved protein motif with the amidase signature family of enzymes. The encoded enzyme is able to catalyze the hydrolysis of a broad range of bioactive lipids, including those from the three main classes of fatty acid amides; N-acylethanolamines, fatty acid primary amides and N-acyl amino acids. This enzyme has a preference for monounsaturated acyl chains as a substrate.[provided by RefSeq, Sep 2009]
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10150R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10150R-A350
Lokale Artikelnummer::
BOSSBS-10150R-A350
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-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5015R-HRP
Lokale Artikelnummer::
BOSSBS-5015R-HRP
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-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10150R-A555
Lokale Artikelnummer::
BOSSBS-10150R-A555
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
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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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