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Image Unavailable-TCIAE0451-25G

Ethyl glutaryl chloride ≥98.0%

Leverantör: TCI EUROPE
Beskrivning: Ethyl glutaryl chloride ≥98.0%

Image Unavailable-TCIAG0202-25ML

Glutaryl dichloride ≥95.0% (by GC, titration analysis)

Artikel nummer : (TCIAG0202-25ML)
Leverantör: TCI EUROPE
Beskrivning: Glutaryl dichloride ≥95.0% (by GC, titration analysis)
UOM: 1 * 25 mL

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Product Image-ACRO119991000

Glutaryl dichloride 97%

Leverantör: Thermo Scientific
Beskrivning: Glutaryl dichloride 97%

Säkerhetsdatablad

Product Image-ACRO126540500

Methyl-5-chloro-5-oxovalerate 98%

Leverantör: Thermo Scientific
Beskrivning: Methyl-5-chloro-5-oxovalerate 98%

Säkerhetsdatablad

Image Unavailable-APOSOR936413-10G

Methyl-5-chloro-5-oxovalerate 95%

Leverantör: Apollo Scientific
Beskrivning: Methyl-5-chloro-5-oxovalerate 95%

Image Unavailable-B25141.18

Methyl-5-chloro-5-oxovalerate 97%

Leverantör: Thermo Scientific
Beskrivning: Methyl-5-chloro-5-oxovalerate 97%

Säkerhetsdatablad Certifikat

Image Unavailable-BOSSBS-13312R-A647

Anti-GCDH Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Artikel nummer : (BOSSBS-13312R-A647)
Leverantör: Bioss
Beskrivning: 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
Image Unavailable-BOSSBS-13312R-CY3

Anti-GCDH Rabbit Polyclonal Antibody (Cy3®)

Artikel nummer : (BOSSBS-13312R-CY3)
Leverantör: Bioss
Beskrivning: 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
Image Unavailable-BOSSBS-13312R-FITC

Anti-GCDH Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Artikel nummer : (BOSSBS-13312R-FITC)
Leverantör: Bioss
Beskrivning: 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
Image Unavailable-BOSSBS-13312R-A750

Anti-GCDH Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Artikel nummer : (BOSSBS-13312R-A750)
Leverantör: Bioss
Beskrivning: 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
Image Unavailable-BOSSBS-13312R-A488

Anti-GCDH Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Artikel nummer : (BOSSBS-13312R-A488)
Leverantör: Bioss
Beskrivning: 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
Image Unavailable-BOSSBS-13312R-A350

Anti-GCDH Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Artikel nummer : (BOSSBS-13312R-A350)
Leverantör: Bioss
Beskrivning: 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
Image Unavailable-BOSSBS-13312R-CY7

Anti-GCDH Rabbit Polyclonal Antibody (Cy7®)

Artikel nummer : (BOSSBS-13312R-CY7)
Leverantör: Bioss
Beskrivning: 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
Image Unavailable-BOSSBS-13312R-A555

Anti-GCDH Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Artikel nummer : (BOSSBS-13312R-A555)
Leverantör: Bioss
Beskrivning: 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
Image Unavailable-BOSSBS-13312R-CY5

Anti-GCDH Rabbit Polyclonal Antibody (Cy5®)

Artikel nummer : (BOSSBS-13312R-CY5)
Leverantör: Bioss
Beskrivning: 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
Image Unavailable-BOSSBS-13312R-HRP

Anti-GCDH Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Artikel nummer : (BOSSBS-13312R-HRP)
Leverantör: Bioss
Beskrivning: 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
Fråga efter pris
Lager för denna produkt är begränsat, men kan vara tillgänglig i ett lager nära dig. Se till att du är inloggad på hemsidan så att tillgängligt lager kan visas. Om call fortfarande visas och du behöver hjälp, ring oss på 08-621 34 20.
Lager för denna produkt är begränsat, men kan vara tillgänglig i ett lager nära dig. Se till att du är inloggad på hemsidan så att tillgängligt lager kan visas. Om call fortfarande visas och du behöver hjälp, ring oss på 08-621 34 20.
VWR International AB säljer bara etanol till skattebefriade kunder. Denna produkt ä reglerad enligt svensk lagstiftning. Om ytterligare information krävs av dig kommer du att kontaktas via e-post.
VWR International AB säljer bara etanol till skattebefriade kunder.
Denna produkt ä reglerad enligt svensk lagstiftning. Om ytterligare information krävs av dig kommer du att kontaktas via email.
Produkten har blockerats av din organisation. Vänligen kontakta din inköpsavdelning för mer information.
Lösenordet och säkerhetsfrågan associerade med ditt Kundnummer har gått ut. Vänligen ändra ditt lösenord och din säkerhetsfråga.
Denna produkt är inte längre tillgänglig. Alternativ kan vara tillgängliga genom att söka med VWR art.nr ovan. Om du behöver ytterligare hjälp, ring VWR Kundservice på 08-621 34 20.
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