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Invitrogen™ EPM2AIP1 Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA521885
Description
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.
Specifications
EPM2AIP1 | |
Polyclonal | |
Unconjugated | |
EPM2AIP1 | |
A930003G21Rik; EPM2A (laforin) interacting protein 1; EPM2A interacting protein 1; EPM2A-interacting protein 1; EPM2AIP1; KIAA0766; Laforin-interacting protein; mKIAA0766; My007 | |
Rabbit | |
Antigen affinity chromatography | |
RUO | |
9852 | |
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
Liquid |
Western Blot | |
1 mg/mL | |
0.1M tris glycine with 10% glycerol and 0.01% thimerosal; pH 7 | |
Q7L775 | |
EPM2AIP1 | |
Synthetic peptide corresponding to a region within amino acids 1 and 43 of EPM2AIP1 (Uniprot ID#Q7L775). | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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