EPM2A Mouse Monoclonal Antibody [Clone ID: k2A3]

SKU AM09050PU-N

EPM2A mouse monoclonal antibody, clone k2A3, Purified

Product Data

• Clone Name: k2A3
• Application: ELISA, FC, WB
• Recommended Dilution: ELISA.; Western blot (1/1,000-1/2,000). ; Flow Cytometry.
• Reactivity: Human
• Antibody Host: Mouse
• Isotype: IgG1
• Clonality: Monoclonal
• Immunogen: Recombinant human EPM2A (aa 243-331) purified from E. coli
• Specificity: The antibody recognizes EPM2A.
• Buffer: PBS, pH 7.4 containing 0.02% Sodium Azide and 10% Glycerol; State: Purified; State: Liquid purified Ig fraction
• Concentration: lot specific
• Purification: Protein-G affinity chromatography
• Conjugation: Unconjugated
• Storage: Store undiluted at 2-8°C for up to two weeks or (in aliquots) at -20°C for longer.; Avoid repeated freezing and thawing.
• Stability: Shelf life: one year from despatch.
• Shipping: Blue Ice
• Gene Name: epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
• Database Link:
  O95278
• Background: Epilepsy, progressive myoclonus type 2A (EPM2A), also known as laforin, is a dual-specificity phosphatase that associates with polyribosomes. The protein may be involved in the control of glycogen metabolism, particularly in monitoring for and preventing the formation of poorly branched glycogen molecules.; Defects in EPM2A are a cause of progressive myoclonic epilepsy type 2(EPM2), also known as Lafora disease. EPM2 is an autosomal recessive and severe form of adolescent-onset progressive epilepsy.
• Synonyms: EPM2A, Laforin, EC=3.1.3.48, EC=3.1.3.16, Lafora PTPase, LAFPTPase

Reference Data