EPM2AIP1 (NM_014805) Human Recombinant Protein
Product Specifications
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
FLJ11207; KIAA0766
Gene ID
9852
UniProt
Q7L775
Accession Number mRNA
NM_014805
Chromosomal Location
3p22.2
Expression System
HEK293T
Tag
C-Myc/DDK
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Molecular Weight
70.2 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
EPM2AIP1
Species
Human
Protein ID
NP_055620
Overview
Recombinant protein of human EPM2A (laforin) interacting protein 1 (EPM2AIP1)
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/9852
Uniprot URL
https://www.uniprot.org/uniprot/Q7L775
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_014805
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_055620
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