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Recommended positive controls: 293T, A431, H1299.
Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
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.
⚠WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: EPM2A (laforin) interacting protein 1; EPM2A-interacting protein 1; Laforin-interacting protein
基因别名: EPM2AIP1; KIAA0766; My007
UniProt ID: (Human) Q7L775
Entrez Gene ID: (Human) 9852