| Product Name | AMPD1 |
|---|---|
| Antibody Type | Primary Antibodies |
| Antigen Alias | AMPD1 antibody; AMP deaminase 1 antibody; AMP deaminase isoform M antibody; Myoadenylate deaminase antibody; |
| Product description | Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene., |
| Immunogen | The antiserum was produced against synthesized peptide derived from human AMPD1. AA range:261-310 |
| Clonality | Polyclonal |
|---|---|
| Isotype | IgG |
| Host Species | Rabbit |
| Tested Applications | IHC |
| IHC:1:100-1:300 |
|
| Species Reactivity | HumanMouseRat |
| Concentration | 1mg/ml |
| Alternative Names | AMPD1 antibody AMP deaminase 1 antibody AMP deaminase isoform M antibody Myoadenylate deaminase antibody |
|---|---|
| Molecular Weight(MW) | kDa |
| SwissProt ID | P23109 |
|---|
| Positive Control | Skeletal muscle, |
|---|---|
| Application Notes | IHC:1:100-1:300 |
| Form | Liquid |
|---|---|
| Storage Instructions | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
| Storage Buffer | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
