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EPM2AIP1


Official Full Name
EPM2A interacting protein 1
Organism
Homo sapiens
Gene ID
9852
Background
The EPM2A gene, which encodes laforin, is mutated in an autosomal recessive form of adolescent progressive myoclonus epilepsy. The protein encoded by this gene binds to laforin, but its function is not known. This gene is intronless. [provided by RefSeq, Oct 2008]
Synonyms
KAT2A; GCN5; hGCN5; GCN5L2; PCAF-b

Cat.No. Product Name Price
SHH036623 shRNA set against Mouse Epm2aip1(NM_175266.4) Inquiry
SHH286557 shRNA set against Human EPM2AIP1 (NM_014805.3) Inquiry
SHH286561 shRNA set against Mouse EPM2AIP1 (NM_175266.4) Inquiry
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MiUTR1M-04438 EPM2AIP1 miRNA 3'UTR clone Inquiry
CDCB158342 Human EPM2AIP1 ORF clone (BC064696) Inquiry
CDCB181507 Rabbit EPM2AIP1 ORF clone (XM_008266130.1) Inquiry
CDCH018751 Mouse EPM2AIP1 ORF clone(NM_175266.4) Inquiry
CDCS413785 Human EPM2AIP1 ORF Clone (BC064696) Inquiry
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