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DMGDH Rabbit anti-Human, Polyclonal, Invitrogen™

Rabbit Polyclonal Antibody

Manufacturer:  Invitrogen PA550021

Catalog No. PA550021


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Description

Description

The antibody detects endogenous levels of total DMGDH protein.

This gene encodes an enzyme involved in the catabolism of choline, catalyzing the oxidative demethylation of dimethylglycine to form sarcosine. The enzyme is found as a monomer in the mitochondrial matrix, and uses flavin adenine dinucleotide and folate as cofactors. Mutation in this gene causes dimethylglycine dehydrogenase deficiency, characterized by a fishlike body odor, chronic muscle fatigue, and elevated levels of the muscle form of creatine kinase in serum. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
Specifications

Specifications

DMGDH
Polyclonal
Unconjugated
DMGDH
Liquid
DMGDH
Synthesized peptide derived from C-terminal of human DMGDH.
Antigen affinity chromatography
RUO
Antibody
Polyclonal
Human
Western Blot
1 mg/mL
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
Q9UI17
dimethylglycine dehydrogenase, mitochondrial, EC 1.5.99.2, M2GD, ME2GLYDH
Rabbit
IgG
100 μL
-20°C
Primary
29958
Documents
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