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Ethyl glutaryl chloride ≥98.0% (by titrimetric analysis)

Fornitore: TCI EUROPE
Descrizione: Ethyl glutaryl chloride ≥98.0% (by titrimetric analysis)

Product Image-ACRO119991000

Glutaryl dichloride 97%

Fornitore: Thermo Scientific
Descrizione: Glutaryl dichloride 97%

MSDS

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Image Unavailable-TCIAG0202-25ML

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

Codice catalogo: (TCIAG0202-25ML)
Fornitore: TCI EUROPE
Codice articolo fornitore: G0202-25ML
Codice articolo locale: TCIAG0202-25ML
Descrizione: Glutaryl dichloride ≥95.0% (by GC, titration analysis)
UOM: 1 * 25 mL
Product Image-ACRO126540500

Methyl-5-chloro-5-oxovalerate 98%

Fornitore: Thermo Scientific
Descrizione: Methyl-5-chloro-5-oxovalerate 98%

MSDS

Image Unavailable-APOSOR936413-10G

Methyl-5-chloro-5-oxovalerate 95%

Fornitore: Apollo Scientific
Descrizione: Methyl-5-chloro-5-oxovalerate 95%

Image Unavailable-B25141.30

Methyl-5-chloro-5-oxovalerate 97%

Fornitore: Thermo Scientific
Descrizione: Methyl-5-chloro-5-oxovalerate 97%

MSDS Certificati

Image Unavailable-BOSSBS-13312R-A647

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

Codice catalogo: (BOSSBS-13312R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-13312R-A647
Codice articolo locale: BOSSBS-13312R-A647
Descrizione: 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-4.90054.1000

1-Ethyl-3-methylimidazolium chloride, Sigma-Aldrich®

Codice catalogo: (4.90054.1000)
Fornitore: Merck
Codice articolo fornitore: 4.90054.1000
Codice articolo locale: MERC4.90054.1000
Descrizione: 1-Ethyl-3-methylimidazolium chloride, Sigma-Aldrich®
UOM: 1 * 1 kg

MSDS


Image Unavailable-BOSSBS-13312R-A488

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

Codice catalogo: (BOSSBS-13312R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-13312R-A488
Codice articolo locale: BOSSBS-13312R-A488
Descrizione: 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®)

Codice catalogo: (BOSSBS-13312R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-13312R-CY3
Codice articolo locale: BOSSBS-13312R-CY3
Descrizione: 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))

Codice catalogo: (BOSSBS-13312R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-13312R-FITC
Codice articolo locale: BOSSBS-13312R-FITC
Descrizione: 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)

Codice catalogo: (BOSSBS-13312R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-13312R-A750
Codice articolo locale: BOSSBS-13312R-A750
Descrizione: 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)

Codice catalogo: (BOSSBS-13312R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-13312R-A350
Codice articolo locale: BOSSBS-13312R-A350
Descrizione: 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®)

Codice catalogo: (BOSSBS-13312R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-13312R-CY7
Codice articolo locale: BOSSBS-13312R-CY7
Descrizione: 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)

Codice catalogo: (BOSSBS-13312R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-13312R-A555
Codice articolo locale: BOSSBS-13312R-A555
Descrizione: 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®)

Codice catalogo: (BOSSBS-13312R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-13312R-CY5
Codice articolo locale: BOSSBS-13312R-CY5
Descrizione: 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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La disponibilità per questo articolo è limitata, ma potrebbe essere disponibile in un magazzino vicino a voi. Si prega di assicurarsi che si è effettuato l'accesso al sito, in modo che ledisponibilità possano essere visualizzati. Se il call è ancora visualizzato e hai bisogno di assistenza, si prega di telefonare a 1-800-932 - 5000.
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