DMGDH Polyclonal Antibody

Background:
dimethylglycine dehydrogenase(DMGDH) Homo sapiens 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],

Alternative Names:
DMGDH, Dimethylglycine dehydrogenase, mitochondrial, ME2GLYDH

Immunogen: The antiserum was produced against synthesized peptide derived from human DMGDH. AA range:817-866

Isotype: Rabbit

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration: 1 mg/ml

Observed band: 97

GeneID: DMGDH

Storage: -20°C/1 year

NOTE: For Research Use Only