| Clonality | polyclonal |
| Host | Rabbit |
| Specificity | Human, Mouse, Rat |
| Tested Application | ELISA, WB |
| Delivery Time | 2 to 4 working days |
| Isotype | IgG |
| Form | liquid |
| Purification | Immunogen affinity purified |
| Purity | ≥95% as determined by SDS-PAGE |
| Uniprot ID | P23109 |
| Gene ID | |
| Calculated MW | 90 kDa |
| Ссылка на страницу на сайте производителя | ссылка |
| Инструкция | PDF |
| Storage | PBS with 0.02% sodium azide and 50% glycerol pH 7.3,-20℃ for 12 months(Avoid repeated freeze / thaw cycles.) |
| Background | AMPD1, also named as MAD and MADA, belongs to the adenosine and AMP deaminases family. AMP deaminase plays a critical role in energy metabolism. It catalyzes the reaction: AMP + H2O = IMP + NH3. Defects in AMPD1 are the cause of adenosine monophosphate deaminase deficiency muscle type(AMPDDM) which is a metabolic disorder resulting in exercise-related myopathy. The antibody is specific to AMPD1. |
| Immunogen | adenosine monophosphate deaminase 1(isoform M) |
| Synonyms | AMPD1, MAD, Myoadenylate deaminase, AMP deaminase isoform M, AMP deaminase 1 |
| Recommended dilution | WB: 1:500-1:5000 |
mouse skeletal muscle tissue were subjected to SDS PAGE followed by western blot with FNab00370(AMPD1-Specific antibody) at dilution of 1:300
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Наименование: anti- AMPD1-Specific antibody.