EPM2A 蛋白
(Epilepsy, Progressive Myoclonus Type 2A, Lafora Disease (Laforin) (EPM2A))
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. [provided by RefSeq, Jul 2008].
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8 results
custom-made
EPM2A
宿主: 小鼠
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
custom-made
EPM2A
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
Aliases for EPM2A 蛋白
EPM2A, laforin glucan phosphatase (EPM2A) 蛋白epilepsy, progressive myoclonic epilepsy, type 2 gene alpha (Epm2a) 蛋白
EPM2A, laforin glucan phosphatase (Epm2a) 蛋白
EPM2 蛋白
laforin 蛋白
MELF 蛋白
Tg(TcraK,TcrbK)TG-BFlv 蛋白
TG-B 蛋白
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