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Arylsulfatase A Antikörper

ARSA Reaktivität: Human, Maus, Ratte WB, FACS Wirt: Maus Monoclonal 4C10 unconjugated
Produktnummer ABIN6654013
  • Target Alle Arylsulfatase A (ARSA) Antikörper anzeigen
    Arylsulfatase A (ARSA)
    Reaktivität
    • 39
    • 32
    • 31
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 44
    • 8
    • 1
    Maus
    Klonalität
    • 47
    • 6
    Monoklonal
    Konjugat
    • 27
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser Arylsulfatase A Antikörper ist unkonjugiert
    Applikation
    • 37
    • 13
    • 12
    • 12
    • 10
    • 10
    • 7
    • 7
    • 6
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), Flow Cytometry (FACS)
    Aufreinigung
    Protein G affinity
    Immunogen
    Amino acids QALKQLQLLKAQLDAAVTFGPSQVARGED were used as the immunogen for the ARSA antibody.
    Klon
    4C10
    Isotyp
    IgG2a
    Top Product
    Discover our top product ARSA Primärantikörper
  • Applikationshinweise
    Optimal dilution of the ARSA antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL,Flow Cytometry: 1-3 μg/10^6 cells
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Buffer
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    Lagerung
    -20 °C
    Informationen zur Lagerung
    After reconstitution, the ARSA antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target
    Arylsulfatase A (ARSA)
    Andere Bezeichnung
    ARSA (ARSA Produkte)
    Hintergrund
    Arylsulfatase A (ARSA) is an enzyme that breaks down sulfatides, namely cerebroside 3-sulfate intocerebroside and sulfate. In humans, arylsulfatase A is encoded by the ARSA gene. ARSA is mapped to 22q13.33. The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Alternatively spliced transcript variants have been described for this gene.
    UniProt
    P15289
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