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Supplier: Thermo Scientific Chemicals
Description: Glutaryl dichloride 97%

Supplier: Ambeed
Description: Glutaroyl dichloride, Purity: 97%, CAS Number: 2873-74-7, Appearance: Liquid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 5G

Catalog Number: (TCG0202-25ML)
Supplier: TCI America
Description: CAS Number: 2873-74-7
MDL Number: MFCD00000755
Molecular Formula: C5H6Cl2O2
Molecular Weight: 169.00
Purity/Analysis Method: >95.0% (GC,T)
Form: Clear Liquid
Boiling point (°C): 218
Flash Point (°C): 106
Specific Gravity (20/20): 1.31

Supplier: TCI America
Description: CAS Number: 5205-39-0
MDL Number: MFCD00013659
Molecular Formula: C7H11ClO3
Molecular Weight: 178.61
Purity/Analysis Method: >98.0% (T)
Form: Clear Liquid
Boiling point (°C): 108
Flash Point (°C): 82
Specific Gravity (20/20): 1.14
Catalog Number: (102656-056)
Supplier: American Radiolabeled Chemicals
Description: Glutaryl-Coenzyme A 0.1 mCi/mL, Glutaryl [1,5-14C]

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Catalog Number: (76576-544)
Supplier: AFG BIOSCIENCE LLC
Description: Human Glutaryl CoA Dehydrogenase, Mitochondrial (GCDH) ELISA Kit, AFG Bioscience


Catalog Number: (MSPP-PAD681HU1)
Supplier: CLOUD-CLONE CORP MS
Description: Polyclonal Antibody to Glutaryl Coenzyme A Dehydrogenase (GCDH), derived from recombinant GCDH (Glu270~Lys438), is reactive with Human/Mouse/Rat/Pig.

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Supplier: Bachem Americas
Description: Sequence: Glutaryl-Phe-AMC

Supplier: TLC Standards
Description: Pharmaceutical Standards, DL-Glutaryl Carnitine-13C-d3 Chloride

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Catalog Number: (102656-058)
Supplier: American Radiolabeled Chemicals
Description: Glutaryl-Coenzyme A 0.1 mCi/mL, [1,5-14C]

Small Business Enterprise


Catalog Number: (75790-920)
Supplier: Prosci
Description: Glutaryl-CoA Dehydrogenase Mitochondrial (GCDH) is an enzyme that acts upon glutaryl-coenzyme A, creating crotonyl-coenzyme A. It plays a role in the metabolism of lysine, hydroxylysine and tryptophan. It uses electron transfer flavoprotein as its electron acceptor. Isoform Short is inactive Glutaryl-CoA and electron-transfer flavoprotein to (E)-but-2-enoyl-CoA, CO2 and reduced electron-transfer flavoprotein. A defect in this enzyme is associated with neurological condition glutaric acidemia type 1 and cause a progressive form of early-onset generalized dystonia.


Supplier: Bachem Americas
Description: Sequence: Glutaryl-Gly-Arg-AMC

Supplier: Ambeed
Description: Methyl-5-chloro-5-oxovalerate 95%

Supplier: Thermo Scientific Chemicals
Description: Methyl-5-chloro-5-oxovalerate 98%

Catalog Number: (10296-016)
Supplier: Bioss
Description: 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.


Supplier: Thermo Scientific Chemicals
Description: 10G
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