EPM2A Rabbit Polyclonal Antibody
Other products for "EPM2A"
Specifications
Product Data | |
Applications | IF, WB |
Recommended Dilution | WB: 1 - 2 ug/mL |
Reactivities | Human, Mouse, Rat |
Host | Rabbit |
Isotype | IgG |
Clonality | Polyclonal |
Immunogen | EPM2A antibody was raised against a 17 amino acid synthetic peptide near the carboxy terminus of human EPM2A. |
Formulation | EPM2A Antibody is supplied in PBS containing 0.02% sodium azide. |
Concentration | 1ug/ul |
Purification | EPM2A Antibody is affinity chromatography purified via peptide column. |
Conjugation | Unconjugated |
Storage | Store at -20°C as received. |
Stability | Stable for 12 months from date of receipt. |
Predicted Protein Size | 36 kDa |
Gene Name | epilepsy, progressive myoclonus type 2A, Lafora disease (laforin) |
Database Link | |
Background | EPM2A Antibody: The Epilepsy, progressive myoclonus type 2A protein (EPM2A) is a dual-specificity phosphatase that associates with polyribosomes. Mutations in this gene have been associated with myoclonic epilepsy of Lafora. EPM2A interacts with a number of proteins known to be involved in glycogen metabolism and has been shown to have robust phosphatase activity against a phosphorylated complex carbohydrate, suggesting that EPM2A may be involved in the regulation of glycogen metabolism. |
Synonyms | EPM2; MELF |
Reference Data | |
Protein Families | Druggable Genome, Phosphatase |
Documents
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