GCDH antibody
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- Target See all GCDH Antibodies
- GCDH (Glutaryl-CoA Dehydrogenase (GCDH))
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Reactivity
- Human, Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This GCDH antibody is un-conjugated
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Application
- Immunohistochemistry (IHC), ELISA
- Characteristics
- Polyclonal Antibody
- Purification
- Antigen affinity purification
- Immunogen
- Fusion protein of human GCDH
- Isotype
- IgG
- Top Product
- Discover our top product GCDH Primary Antibody
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- Application Notes
- IHC 1:30-1:150, ELISA 1:5000-1:10000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1.02 mg/mL
- Buffer
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- GCDH (Glutaryl-CoA Dehydrogenase (GCDH))
- Alternative Name
- GCDH (GCDH Products)
- Synonyms
- ACAD5 antibody, GCD antibody, zgc:56505 antibody, zgc:77704 antibody, 9030411L18 antibody, AI266902 antibody, D17825 antibody, glutaryl-CoA dehydrogenase antibody, glutaryl-CoA dehydrogenase a antibody, glutaryl-Coenzyme A dehydrogenase antibody, GCDH antibody, Gcdh antibody, gcdha antibody
- Background
- The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family. It catalyzes 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. It uses electron transfer flavoprotein as its electron acceptor. The enzyme exists in the mitochondrial matrix as a homotetramer of 45-kD subunits. Mutations in this gene result in the metabolic disorder glutaric aciduria type 1, which is also known as glutaric acidemia type I. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 12.
- UniProt
- Q92947
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