PYGM Polyclonal Antibody (E-AB-15321)
For research use only.
| Verified Samples |
Verified Samples in WB: Mouse heart Verified Samples in IHC: Human thyroid cancer, Human liver cancer |
| Dilution | WB 1:500-1:2000, IHC 1:30-1:150 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Applications | WB, IHC |
| Clonality | Polyclonal |
| Immunogen | Recombinant protein of human PYGM |
| Abbre | PYGM |
| Synonyms | Glycogen phosphorylase, Glycogen phosphorylase muscle form, Muscpho, Myophosphorylase, PYGM, Phosphorylase glycogen muscle (McArdle syndrome glycogen storage disease type V), Pygm, muscle form |
| Swissprot | |
| Calculated MW | 97 kDa |
| Cellular Localization | Cytosol, Extracellular region or secreted, extracellular exosome, Other locations: cytoplasm. |
| Concentration | 0.4 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | Cancer, Metabolism, Signal Transduction |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
| background | This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants. |
Other Clones
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Other Formats
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Unconjugated
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