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Specification
| Full name | AMPD1 rabbit polyclonal antibody |
| Alternative names | 50 μl/100 μl |
| Reactivity | rabbit polyclonal |
| Applications | WB, IHC |
| Host | Rabbit |
| Clone type | rabbit polyclonal |
| Target Background | 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. |
| Swissprot No | P23109 |
| Gene Accession | NP_000027 |
| WB Predicted band size | Immunohistochemical analysis of paraffin-embedded Human lung cancer tissue or AMPD1 antigen-treated (Neutralization experiment) using P102536(AMPD1 Antibody) at dilution 1/80 |
| WB Positive control | P102536-WB-1-P |
| WB Recommended dilution | 90 kDa |
| IHC predicted cell location | Predicted cell location: Cytoplasm |
| IHC positive control | Positive control: Human liver cancer |
| IHC Recommed dilution | Recommended dilution: 100-300 |
Storage
-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
WB PIC Description
P102536-WB-1-P
IHC PIC Description
Immunohistochemical analysis of paraffin-embedded Human liver cancer tissue or AMPD1 antigen-treated (Neutralization experiment) using P102536(AMPD1 Antibody) at dilution 1/80
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We also provide express shippping for time-sensitive deliveries.
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