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Invitrogen™ DMGDH Polyclonal Antibody
Rabbit Polyclonal Antibody
Brand: Invitrogen™ PA550021
This item is not returnable.
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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.
Specifications
| DMGDH | |
| Polyclonal | |
| Unconjugated | |
| DMGDH | |
| 1200014D15Rik; AI787269; dimethylglycine dehydrogenase; dimethylglycine dehydrogenase precursor; dimethylglycine dehydrogenase, mitochondrial; Dmgdh; DMGDHD; EC 1.5.99.2; M2GD; ME2GLYDH | |
| Rabbit | |
| Antigen affinity chromatography | |
| RUO | |
| 29958 | |
| -20°C | |
| Liquid |
| Western Blot | |
| 1 mg/mL | |
| PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 | |
| Q9UI17 | |
| DMGDH | |
| Synthesized peptide derived from C-terminal of human DMGDH. | |
| 100 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG |
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