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DMGDH
Dimethylglycine dehydrogenaseThis 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]
Top validated antibodies |
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| Proteintech Group |  24813-1-AP |
3 references | Polyclonal |
WB
EL
IHC
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| Cusabio Biotech Co., Ltd | CSB-PA883415LA01HU |
Polyclonal |
WB
EL
ICC
IHC
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| LSBio | LS-C368698 |
Polyclonal |
WB
IHC
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| Biorbyt | orb417499 |
Polyclonal |
WB
EL
ICC
IHC
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| Invitrogen Antibodies | PA5-113450 |
Polyclonal |
WB
EL
ICC
IHC
|
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