DMGDH Polyclonal Antibody | G-AB-03650

DMGDH Polyclonal Antibody | G-AB-03650 | Gentaur Antibodies

Overview: 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.

Category Type: Polyclonal Antibody

Research Areas: Metabolism, Neuroscience, Signal Transduction

Synonyms: Dimethylglycine dehydrogenase, Dimethylglycine dehydrogenase, mitochondrial, Dmgdh, M2GD, ME2GLYDH, mitochondrial

Reactivity: Human

Host: Rabbit

Isotype: IgG

Gene ID:

Accession #: NP037523

Clonality: Polyclonal

Immunogen: Synthetic peptide of human DMGDH

Clone #:

Conjugation: Unconjugated

Swissprot: Q9UI17

Santa Cruz:

Calculated MW: 97 kDa

Observed MW: Refer to figures

Concentration: 2.1 mg/mL

Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

Purification method: Antigen affinity purification

Application: WB, ELISA

Dilution: WB 1:500-1:2000, ELISA 1:5000-1:10000

Storage: Store at -20°C. Avoid freeze / thaw cycles.

DMGDH Polyclonal Antibody DataSheet