DMGDH rabbit pAb
Product Sizes
50UL
£ POA
ES2179-50UL
100UL
£ POA
ES2179-100UL
About this Product
- SKU:
- ES2179
- Additional Names:
- DMGDH; Dimethylglycine dehydrogenase; mitochondrial; ME2GLYDH
- Application:
- Western Blot, Immunohistochemistry, Immunofluorescence, ELISA
- Clonality:
- Polyclonal
- Concentration:
- 1 mg/ml
- Extra Details:
- 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];
- Immunogen:
- The antiserum was produced against synthesized peptide derived from human DMGDH. AA range:817-866
- Isotype:
- IgG
- Reactivities:
- Human, Rat, Mouse
- Shipping Conditions:
- Blue Ice
- Source:
- Rabbit
- Storage Conditions:
- -20[o]C
- Supplier:
- ELK Biotechnology
- Type:
- Antibodies: Polyclonal Antibody
