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AAV2 Antikörper (N-Term)

AAV2 Reaktivität: Adeno-Associated Virus 2 (AAV-2) WB Wirt: Maus Monoclonal 303-9 unconjugated
Produktnummer ABIN452139
  • Target Alle AAV2 Produkte
    AAV2 (Adeno-Associated Virus 2 (AAV2))
    Bindungsspezifität
    N-Term
    Reaktivität
    Adeno-Associated Virus 2 (AAV-2)
    Wirt
    • 6
    Maus
    Klonalität
    • 6
    Monoklonal
    Konjugat
    • 5
    • 1
    Dieser AAV2 Antikörper ist unkonjugiert
    Applikation
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Produktmerkmale
    Synonyms: AAV2
    Aufreinigung
    Protein A Affinity Chromatography
    Immunogen
    Recombinant AAV-2 Rep 78 protein, N-terminally truncated by 171 aa
    Klon
    303-9
    Isotyp
    IgG1
  • Applikationshinweise
    Western Blot: 1/50 - 1/100.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Rekonstitution
    Restore in 1 mL dist. water
    Buffer
    (final solution contains 0.09 % NaN3, 0.5 % BSA in PBS buffer, pH 7.4)
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    Prior to reconstitution store at 2-8 °C. Following reconstitution store the antibody at -20 °C. Avoid repeated freezing and thawing.
    Shelf life: one year from despatch.
    Haltbarkeit
    12 months
  • Target
    AAV2 (Adeno-Associated Virus 2 (AAV2))
    Andere Bezeichnung
    Adeno-Associated Virus 2 / AAV2 (AAV2 Produkte)
    Substanzklasse
    Virus
    Hintergrund
    Adeno-associated virus (AAV) is a small virus which infects humans and some other primate species. AAV is not currently known to cause disease and consequently the virus causes a very mild immune response. AAV can infect both dividing and non-dividing cells and may incorporate its genome into that of the host cell. These features make AAV a very attractive candidate for creating viral vectors for gene therapy, and for the creation of isogenic human disease models. Serotype 2 (AAV2) has been the most extensively examined so far. AAV2 presents natural tropism towards skeletal muscles, neurons, vascular smooth muscle cells and hepatocytes.Synonyms: AAV-2
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