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WB analysis of HeLa and 293T lysates (20ug per lane) using EPM2A antibody at a dilution of 1:1,000.
WB analysis of HeLa and 293T lysates (20ug per lane) using EPM2A antibody at a dilution of 1:1,000.
WB analysis of HeLa and 293T lysates (20ug per lane) using EPM2A antibody at a dilution of 1:1,000.

Laforin antibody [k2A3]

GTX53711
GeneTex
ApplicationsWestern Blot, ELISA
Product group Antibodies
ReactivityHuman
TargetEPM2A
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Overview

  • Supplier
    GeneTex
  • Product Name
    Laforin antibody [k2A3]
  • Delivery Days Customer
    9
  • Application Supplier Note
    The antibody has been tested by ELISA and Western blot analysis to assure specificity and reactivity. Since application varies, however, each investigation should be titrated by the reagent to obtain optimal results. Recommended dilution range for Western blot analysis is 1:1,000 ~ 2,000. Recommended starting dilution is 1:1,000.
  • Applications
    Western Blot, ELISA
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    k2A3
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID7957
  • Target name
    EPM2A
  • Target description
    EPM2A glucan phosphatase, laforin
  • Target synonyms
    epilepsy, progressive myoclonus type 2, Lafora disease (laforin); epilepsy, progressive myoclonus type 2A, Lafora disease (laforin); EPM2; EPM2A, laforin glucan phosphatase; glucan phosphatase; glycogen phosphatase; lafora PTPase; laforin; LAFPTPase; MELF
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDO95278
  • Protein Name
    Laforin
  • Scientific Description
    This gene encodes a dual-specificity phosphatase and may be involved in the regulation of glycogen metabolism. The protein acts on complex carbohydrates to prevent glycogen hyperphosphorylation, thus avoiding the formation of insoluble aggregates. Loss-of-function mutations in this gene have been associated with Lafora disease, a rare, adult-onset recessive neurodegenerative disease, which results in myoclonus epilepsy and usually results in death several years after the onset of symptoms. The disease is characterized by the accumulation of insoluble particles called Lafora bodies, which are derived from glycogen. [provided by RefSeq, Jan 2018]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203