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Du søkte etter: Ethyl+glutaryl+chloride


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Image Unavailable-TCIAE0451-25G

Ethyl glutaryl chloride ≥98.0% (by titrimetric analysis)

Produsent: TCI
Beskrivelse: Ethyl glutaryl chloride ≥98.0% (by titrimetric analysis)

Image Unavailable-TCIAG0202-25ML

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

Artikkenummer: (TCIAG0202-25ML)
Produsent: TCI
Beskrivelse: Glutaryl dichloride ≥95.0% (by GC, titration analysis)
UOM: 1 * 25 mL

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Product Image-ACRO126540500

Methyl-5-chloro-5-oxovalerate 98%

Produsent: Thermo Scientific
Beskrivelse: Methyl-5-chloro-5-oxovalerate 98%

HMS

Product Image-ACRO119990250

Glutaryl dichloride 97%

Produsent: Thermo Scientific
Beskrivelse: Glutaryl dichloride 97%

HMS

Image Unavailable-B25141.30

Methyl-5-chloro-5-oxovalerate 97%

Produsent: Thermo Scientific
Beskrivelse: Methyl-5-chloro-5-oxovalerate 97%

HMS Sertifikater

Image Unavailable-APOSOR936413-25G

Methyl-5-chloro-5-oxovalerate 95%

Produsent: Apollo Scientific
Beskrivelse: Methyl-5-chloro-5-oxovalerate 95%

Image Unavailable-BOSSBS-13312R-A647

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

Artikkenummer: (BOSSBS-13312R-A647)
Produsent: Bioss
Beskrivelse: 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®

Artikkenummer: (4.90054.1000)
Produsent: Merck
Beskrivelse: 1-Ethyl-3-methylimidazolium chloride, Sigma-Aldrich®
UOM: 1 * 1 kg

HMS


Image Unavailable-BOSSBS-13312R-CY5

Anti-GCDH Rabbit Polyclonal Antibody (Cy5®)

Artikkenummer: (BOSSBS-13312R-CY5)
Produsent: Bioss
Beskrivelse: 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-A680

Anti-GCDH Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Artikkenummer: (BOSSBS-13312R-A680)
Produsent: Bioss
Beskrivelse: 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))

Artikkenummer: (BOSSBS-13312R-HRP)
Produsent: Bioss
Beskrivelse: 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®)

Artikkenummer: (BOSSBS-13312R-CY3)
Produsent: Bioss
Beskrivelse: 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))

Artikkenummer: (BOSSBS-13312R-FITC)
Produsent: Bioss
Beskrivelse: 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)

Artikkenummer: (BOSSBS-13312R-A488)
Produsent: Bioss
Beskrivelse: 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)

Artikkenummer: (BOSSBS-13312R-A750)
Produsent: Bioss
Beskrivelse: 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)

Artikkenummer: (BOSSBS-13312R-A555)
Produsent: Bioss
Beskrivelse: 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
Pris på forespørsel
Lager for dette produktet er begrenset, men kan være tilgjengelig i en lagerbygning i nærheten av deg. Vennligst sørg for at du er logget inn på nettstedet, slik at tilgjengelige lager kan vises. Hvis call er fortsatt vises og du trenger hjelp, kan du ringe oss på 1-800-932 - 5000.
Lager for dette punktet er begrenset, men kan være tilgjengelig i en lagerbygning i nærheten av deg. Vennligst sørg for at du er logget inn på nettstedet, slik at tilgjengelige lager kan vises. Hvis call er fortsatt vises og du trenger hjelp, kan du ringe oss på 1-800-932 - 5000.
NB Dette produkt er regulert i henhold til norsk lov.
Dersom ytterligere informasjon er nødvendig fra deg vil du bli kontaktet av VWR via e-post.
OBS! Etanol er underlagt bestemmelse om særavgift, jfr LOV-1993-05-19-11-§1. VWR selger kun etanol til kunder som kan fremlegge avgiftsfritak for udenaturert etanol, jfr. § 3-3-7 ( forskrifter om særavgifter).
NB Dette produkt er regulert i henhold til norsk lov.
Dersom ytterligere informasjon er nødvendig fra deg vil du bli kontaktet av VWR via e-post.
OBS! Etanol er underlagt bestemmelse om særavgift, jfr LOV-1993-05-19-11-§1. VWR selger kun etanol til kunder som kan fremlegge avgiftsfritak for udenaturert etanol, jfr. § 3-3-7 ( forskrifter om særavgifter).
Dette produktet har blitt blokkert for din organisasjon. Ta kontakt med din innkjøpsavdeling for mer informasjon.
Det opprinnelige produktet er ikke lenger tilgjengelig. Varen som vises er tilgjengelig.
Produkt (er) merket med dette symbolet er ikke lenger tilgjengelig og selges til lageret er tomt. Alternativer kan være tilgjengelige ved å søke med VWR Katalognummer ovenfor. Hvis du trenger ytterligere hjelp, ring VWR kundeservice 22900000
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