"EPM2A" Related Products

Recombinant Human EPM2A cell lysate

Cat.No.: EPM2A-568HCL
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;
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;

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