Recombinant Human EPM2A cell lysate

• Cat.No.: EPM2A-568HCL

Specification

• Description: This gene encodes a dual-specificity phosphatase that associates with polyribosomes. The encoded protein may be involved in the regulation of glycogen metabolism. Mutations in this gene have been associated with myoclonic epilepsy of Lafora. Alternative splicing results in multiple transcript variants.
• Species: Human
• Size: 100 ul
• Storage Buffer: 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
• Applications: Western Blot
• Tag: Non

Gene Information

• Gene Name: EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin) [ Homo sapiens ]
• Official Symbol: EPM2A
• Synonyms: EPM2A; epilepsy, progressive myoclonus type 2A, Lafora disease (laforin); epilepsy, progressive myoclonus type 2, Lafora disease (laforin); laforin; LD; LDE; LAFPTPase; lafora PTPase; EPM2; MELF
• Gene ID: 7957
• mRNA Refseq: NM_001018041
• Protein Refseq: NP_001018051
• MIM: 607566
• UniProt ID: B3EWF7
• Chromosome Location: 6q24
• Function: carbohydrate binding; hydrolase activity; protein binding; protein serine/threonine phosphatase activity; protein serine/threonine phosphatase activity; protein tyrosine phosphatase activity; protein tyrosine phosphatase activity; protein tyrosine/serine/threonine phosphatase activity; starch binding