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Dimethylglycine dehydrogenase

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Catalyzes the demethylation of N,N-dimethylglycine to sarcosine. Also has activity with sarcosine in vitro.

Below are the list of possible Dimethylglycine dehydrogenase products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Dimethylglycine dehydrogenase

 Dimethylglycine dehydrogenase ELISA Kit
 Dimethylglycine dehydrogenase Recombinant
 Dimethylglycine dehydrogenase Antibody
Also known as Dimethylglycine dehydrogenase, mitochondrial (ME2GLYDH).
DMGDH: Defects in DMGDH are the cause of DMGDH deficiency (DMGDHD). DMGDHD is a disorder characterized by fish odor, muscle fatigue with increased serum creatine kinase. Biochemically it is characterized by an increase of N,N- dimethylglycine (DMG) in serum and urine. Belongs to the GcvT family.

Protein type: Amino Ac
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id Metabolism - glycine, serine and threonine; EC 1.5.8.4; Mitochondrial; Oxidoreductase

Cellular Component: mitochondrion

Molecular Function: dimethylglycine dehydrogenase activity; FAD binding; folic acid binding

Biological Process: choline catabolic process; choline metabolic process; glycine metabolic process
 Dmgdh ELISA Kit
 Dmgdh Recombinant
 Dmgdh Antibody
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