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EPM2AIP1 Antibody

Novus Biologicals, part of Bio-Techne | Catalog # NBP1-31063

Novus Biologicals, part of Bio-Techne
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NBP1-31063

Key Product Details

Species Reactivity

Human

Applications

Western Blot

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Concentration

Concentrations vary lot to lot. See vial label for concentration. If unlisted please contact technical services.

Product Specifications

Immunogen

Carrier-protein conjugated synthetic peptide encompassing a sequence within the N-terminus region of human EPM2AIP1. The exact sequence is proprietary.

Reactivity Notes

Immunogen displays the following percentage of sequence identity for non-tested species: Mouse (83%) and Rat (83%).

Localization

Endoplasmic reticulum

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Theoretical MW

70 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Scientific Data Images for EPM2AIP1 Antibody

Western Blot: EPM2AIP1 Antibody [NBP1-31063]

Western Blot: EPM2AIP1 Antibody [NBP1-31063]

Western Blot: EPM2AIP1 Antibody [NBP1-31063] - Sample(30 ug of whole cell lysate)A:293TB:A431 C:H12997. 5% SDS PAGE, antibody diluted at 1:500.

Applications for EPM2AIP1 Antibody

Application
Recommended Usage

Western Blot

1:500-1:3000

Formulation, Preparation, and Storage

Purification

Antigen Affinity-purified

Formulation

0.1M Tris (pH 7), 0.1M Glycine, 10% Glycerol

Preservative

0.01% Thimerosal

Concentration

Concentrations vary lot to lot. See vial label for concentration. If unlisted please contact technical services.

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.

Background: EPM2AIP1

EPM2A is a dual specificity protein phosphatase that associates with polyribosomes. It may be involved in the control of glycogen metabolism, particularly in monitoring for and preventing the formation of poorly branched glycogen molecules (polyglucosans). Defects in EPM2A are a cause of Lafora disease (LD); also known as myoclonic epilepsy of Lafora (MELF) or epilepsy progressive myoclonic 2 (EPM2). LD is the most common and severe form of adolescent-onset progressive epilepsy.

Alternate Names

EPM2A (laforin) interacting protein 1, EPM2A interacting protein 1, EPM2A-interacting protein 1, KIAA0766FLJ11207, Laforin-interacting protein

Gene Symbol

EPM2AIP1

Additional EPM2AIP1 Products

Product Documents for EPM2AIP1 Antibody

Certificate of Analysis

To download a Certificate of Analysis, please enter a lot number in the search box below.

Product Specific Notices for EPM2AIP1 Antibody

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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⚠ WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause reproductive toxicity with developmental effects.  For more information go to www.P65Warnings.ca.gov.