EPM2AIP1 Mouse Monoclonal Antibody [Kloon ID: LBI2A5]

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]. COMPLETENESS: complete on the 3' end.

Carrier-free (BSA/glycerol-free) EPM2AIP1 mouse monoclonal antibody, clone LBI2A5

FLJ11207; KIAA0766

Homo sapiens EPM2A interacting protein 1 (EPM2AIP1), mRNA.

9852

Q7L775

Unconjugated

WB 1:500~2000, IF 1:100, FLOW 1:100

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

EPM2AIP1

https://www.ncbi.nlm.nih.gov/gene/?term=9852

https://www.uniprot.org/uniprot/Q7L775