Application
Western blot analysis of extracts from HT-29/A549 cells, using DMGDH Antibody. The lane on the right is treated with the synthesized peptide.| Product Name | DMGDH antibody |
|---|---|
| Antibody Type | Primary Antibodies |
| Product description | Rabbit polyclonal antibody to DMGDHThis 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. [provided by RefSeq] |
| Immunogen | The antiserum was produced against synthesized peptide derived from human DMGDH. |
| Clonality | Polyclonal |
|---|---|
| Host Species | Rabbit |
| Tested Applications | ELISAWB |
| ELISA: 1:20000Optimal dilutions should be determined experimentally by the end user.: |
|
| Species Reactivity | Human |
| Concentration | 1mg/ml |
| Purification | Affinity purified |
| Gene Synonyms | EC1.5.99.2 ME2GLYDH EC 1.5.99.2 mitochondrial Dimethylglycine dehydrogenase DMGDH |
|---|---|
| Target | DMGDH |
| Molecular Weight(MW) | 96 kDa (note) |
| Tissue Specificity | DMGDH Antibody detects endogenous levels of total DMGDH protein. |
Application
Western blot analysis of extracts from HT-29/A549 cells, using DMGDH Antibody. The lane on the right is treated with the synthesized peptide.| Application Notes | ELISA: 1:20000Optimal dilutions should be determined experimentally by the end user.: |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | Store at -20 degrees Celcius. Product is stable for at least 1 year. |
| Storage Buffer | Phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. |
