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EPM2A Antikörper (AA 243-331)

EPM2A Reaktivität: Human WB, ELISA, IF, ICC Wirt: Maus Monoclonal k2A3 unconjugated
Produktnummer ABIN533790
  • Target Alle EPM2A Antikörper anzeigen
    EPM2A (Epilepsy, Progressive Myoclonus Type 2A, Lafora Disease (Laforin) (EPM2A))
    Bindungsspezifität
    • 10
    • 8
    • 8
    • 6
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 243-331
    Reaktivität
    • 43
    • 8
    • 7
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    Human
    Wirt
    • 34
    • 8
    • 2
    Maus
    Klonalität
    • 38
    • 6
    Monoklonal
    Konjugat
    • 29
    • 4
    • 4
    • 3
    • 2
    • 2
    Dieser EPM2A Antikörper ist unkonjugiert
    Applikation
    • 32
    • 25
    • 23
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)
    Verwendungszweck
    Mouse monoclonal antibody raised against partial recombinant EPM2A.
    Kreuzreaktivität
    Human
    Produktmerkmale
    Antibody Reactive Against Recombinant Protein.
    Immunogen
    Recombinant protein corresponding to amino acids 243-331 of human EPM2A.
    Klon
    K2A3
    Isotyp
    IgG1
    Top Product
    Discover our top product EPM2A Primärantikörper
  • Applikationshinweise
    The optimal working dilution should be determined by the end user.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    In PBS, pH 7.4 (10 % glycerol, 0.02 % sodium azide).
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C,-80 °C
    Informationen zur Lagerung
    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." in: 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." in: 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." in: Human molecular genetics, Vol. 11, Issue 11, pp. 1263-71, (2002) (PubMed).

  • Target
    EPM2A (Epilepsy, Progressive Myoclonus Type 2A, Lafora Disease (Laforin) (EPM2A))
    Andere Bezeichnung
    Laforin (EPM2A Produkte)
    Synonyme
    TG-B antikoerper, Tg(TcraK,TcrbK)TG-BFlv antikoerper, EPM2 antikoerper, MELF antikoerper, laforin antikoerper, EPM2A, laforin glucan phosphatase antikoerper, epilepsy, progressive myoclonic epilepsy, type 2 gene alpha antikoerper, EPM2A antikoerper, Epm2a antikoerper
    Gen-ID
    7957
    Pathways
    Cellular Glucan Metabolic Process
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