DMGDH Antibody (C-term) Blocking Peptide
€363.00
In stock
SKU
AC-BP18005b
Background:
This gene encodes an enzyme involved in the catabolism ofcholine, catalyzing the oxidative demethylation of dimethylglycineto form sarcosine. The enzyme is found as a monomer in themitochondrial matrix, and uses flavin adenine dinucleotide andfolate as cofactors. Mutation in this gene causes dimethylglycinedehydrogenase deficiency, characterized by a fishlike body odor,chronic muscle fatigue, and elevated levels of the muscle form ofcreatine kinase in serum.
Other Names:
Dimethylglycine dehydrogenase, mitochondrial, ME2GLYDH, DMGDH
Gene Name: DMGDH
Gene ID: 29958
Primary Accession: Q9UI17
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
This gene encodes an enzyme involved in the catabolism ofcholine, catalyzing the oxidative demethylation of dimethylglycineto form sarcosine. The enzyme is found as a monomer in themitochondrial matrix, and uses flavin adenine dinucleotide andfolate as cofactors. Mutation in this gene causes dimethylglycinedehydrogenase deficiency, characterized by a fishlike body odor,chronic muscle fatigue, and elevated levels of the muscle form ofcreatine kinase in serum.
Other Names:
Dimethylglycine dehydrogenase, mitochondrial, ME2GLYDH, DMGDH
Gene Name: DMGDH
Gene ID: 29958
Primary Accession: Q9UI17
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
| Is Featured? | No |
|---|
Write Your Own Review