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AAV2 anticorps (N-Term)

AAV2 Reactivité: Adeno-Associated Virus 2 (AAV-2) WB Hôte: Souris Monoclonal 303-9 unconjugated
N° du produit ABIN452139
  • Antigène Tous les produits AAV2
    AAV2 (Adeno-Associated Virus 2 (AAV2))
    Épitope
    N-Term
    Reactivité
    Adeno-Associated Virus 2 (AAV-2)
    Hôte
    • 5
    Souris
    Clonalité
    • 5
    Monoclonal
    Conjugué
    • 4
    • 1
    Cet anticorp AAV2 est non-conjugé
    Application
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Attributs du produit
    Synonyms: AAV2
    Purification
    Protein A Affinity Chromatography
    Immunogène
    Recombinant AAV-2 Rep 78 protein, N-terminally truncated by 171 aa
    Clone
    303-9
    Isotype
    IgG1
  • Indications d'application
    Western Blot: 1/50 - 1/100.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.
    Restrictions
    For Research Use only
  • Reconstitution
    Restore in 1 mL dist. water
    Buffer
    (final solution contains 0.09 % NaN3, 0.5 % BSA in PBS buffer, pH 7.4)
    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
    4 °C/-20 °C
    Stockage commentaire
    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.
    Date de péremption
    12 months
  • Antigène
    AAV2 (Adeno-Associated Virus 2 (AAV2))
    Autre désignation
    Adeno-Associated Virus 2 / AAV2 (AAV2 Produits)
    Classe de substances
    Virus
    Sujet
    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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