Sie suchten nach: DSG+(Disuccinimidyl+glutarate)

Artikel-Nr: (MOLEM31532919)

Lieferant: Molekula

Hersteller Artikel Nummer : M31532919

Beschreibung: Glutaraldehyd 50% in wässriger Lösung

UOM: 1 * 1 L

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Artikel-Nr: (BOSSBS-13312R-A555)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13312R-A555

Beschreibung: GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-13312R-CY7)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13312R-CY7

Beschreibung: GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-13312R-A350)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13312R-A350

Beschreibung: GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.

UOM: 1 * 100 µl

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Lieferant: Roth Carl

Beschreibung: Glutaraldehyd 25% in wässriger Lösung

Artikel-Nr: (BOSSBS-13312R-A488)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13312R-A488

Beschreibung: GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-13312R-CY5)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13312R-CY5

Beschreibung: GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-13312R-A680)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13312R-A680

Beschreibung: GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.

UOM: 1 * 100 µl

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Artikel-Nr: (MOLEM11019138)

Lieferant: Molekula

Hersteller Artikel Nummer : M11019138

Beschreibung: Glutarsäure

UOM: 1 * 100 g

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Artikel-Nr: (MOLE20533442-500G)

Lieferant: Molekula

Hersteller Artikel Nummer : 20533442-500G

Beschreibung: Glutarsäureanhydrid

UOM: 1 * 500 g

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Artikel-Nr: (EHERC14034500)

Lieferant: EHRENSTORFER

Hersteller Artikel Nummer : C14034500

Beschreibung: Glutarsäure

UOM: 1 * 0,25 g

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Artikel-Nr: (354400-500)

Lieferant: Merck Millipore (Calbiochem‎)

Hersteller Artikel Nummer : 354400-500

Beschreibung: Glutaraldehyd 25% in wässriger Lösung, Sigma-Aldrich®

UOM: 1 * 500 mL

Zertifikate Sale

Artikel-Nr: (BOSSBS-0494R-A750)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-0494R-A750

Beschreibung: ETFA participates in catalyzing the initial step of the mitochondrial fatty acid beta-oxidation. It shuttles electrons between primary flavoprotein dehydrogenases and the membrane-bound electron transfer flavoprotein ubiquinone oxidoreductase. Defects in electron-transfer-flavoprotein have been implicated in type II glutaricaciduria in which multiple acyl-CoA dehydrogenase deficiencies result in large excretion of glutaric, lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids. Two transcript variants encoding different isoforms have been found for this gene.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-0494R-CY5)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-0494R-CY5

Beschreibung: ETFA participates in catalyzing the initial step of the mitochondrial fatty acid beta-oxidation. It shuttles electrons between primary flavoprotein dehydrogenases and the membrane-bound electron transfer flavoprotein ubiquinone oxidoreductase. Defects in electron-transfer-flavoprotein have been implicated in type II glutaricaciduria in which multiple acyl-CoA dehydrogenase deficiencies result in large excretion of glutaric, lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].

UOM: 1 * 100 µl

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Artikel-Nr: (ROTH4157.1)

Lieferant: Roth Carl

Hersteller Artikel Nummer : 4157.1

Beschreibung: Glutaraldehyd 25% in wässriger Lösung

UOM: 1 * 25 g

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Lieferant: EUROCLONE

Beschreibung: Glutaraldehyd 50% in wässriger Lösung