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EPM2A anticorps (AA 243-331)

EPM2A Reactivité: Humain WB, ELISA, IF, ICC Hôte: Souris Monoclonal k2A3 unconjugated
N° du produit ABIN533790
  • Antigène Voir toutes EPM2A Anticorps
    EPM2A (Epilepsy, Progressive Myoclonus Type 2A, Lafora Disease (Laforin) (EPM2A))
    Épitope
    • 10
    • 8
    • 8
    • 6
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 243-331
    Reactivité
    • 43
    • 8
    • 7
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    Humain
    Hôte
    • 34
    • 8
    • 2
    Souris
    Clonalité
    • 38
    • 6
    Monoclonal
    Conjugué
    • 29
    • 4
    • 4
    • 3
    • 2
    • 2
    Cet anticorp EPM2A est non-conjugé
    Application
    • 32
    • 25
    • 23
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)
    Fonction
    Mouse monoclonal antibody raised against partial recombinant EPM2A.
     Réactivité croisée
    Humain
    Attributs du produit
    Antibody Reactive Against Recombinant Protein.
    Immunogène
    Recombinant protein corresponding to amino acids 243-331 of human EPM2A.
    Clone
    K2A3
    Isotype
    IgG1
    Top Product
    Discover our top product EPM2A Anticorps primaire
  • Indications d'application
    The optimal working dilution should be determined by the end user.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    In PBS, pH 7.4 (10 % glycerol, 0.02 % sodium azide).
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C,-80 °C
    Stockage commentaire
    Store at 2°C to 8°C for 1 week. For long term storage, aliquot and store at -20°C to -80°C.
    Aliquot to avoid repeated freezing and thawing.
  • Tagliabracci, Turnbull, Wang, Girard, Zhao, Skurat, Delgado-Escueta, Minassian, Depaoli-Roach, Roach: "Laforin is a glycogen phosphatase, deficiency of which leads to elevated phosphorylation of glycogen in vivo." dans: Proceedings of the National Academy of Sciences of the United States of America, Vol. 104, Issue 49, pp. 19262-6, (2007) (PubMed).

    Wang, Parker, Skurat, Raben, DePaoli-Roach, Roach: "Relationship between glycogen accumulation and the laforin dual specificity phosphatase." dans: Biochemical and biophysical research communications, Vol. 350, Issue 3, pp. 588-92, (2006) (PubMed).

    Ganesh, Delgado-Escueta, Suzuki, Francheschetti, Riggio, Avanzini, Rabinowicz, Bohlega, Bailey, Alonso, Rasmussen, Thomson, Ochoa, Prado, Medina, Yamakawa: "Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype." dans: Human molecular genetics, Vol. 11, Issue 11, pp. 1263-71, (2002) (PubMed).

  • Antigène
    EPM2A (Epilepsy, Progressive Myoclonus Type 2A, Lafora Disease (Laforin) (EPM2A))
    Autre désignation
    Laforin (EPM2A Produits)
    Synonymes
    anticorps TG-B, anticorps Tg(TcraK,TcrbK)TG-BFlv, anticorps EPM2, anticorps MELF, anticorps laforin, anticorps EPM2A, laforin glucan phosphatase, anticorps epilepsy, progressive myoclonic epilepsy, type 2 gene alpha, anticorps EPM2A, anticorps Epm2a
    ID gène
    7957
    Pathways
    Cellular Glucan Metabolic Process
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