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AAV2 anticorps (N-Term)

Cet anticorps anti-AAV2 est un anticorps Souris Monoclonal détectant AAV2 dans WB. Adapté pour Adeno-Associated Virus 2 (AAV-2).
N° du produit ABIN452139

Aperçu rapide pour AAV2 anticorps (N-Term) (ABIN452139)

Antigène

AAV2 (Adeno-Associated Virus 2 (AAV2))

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)

Clone

303-9
  • Épitope

    N-Term

    Attributs du produit

    Synonyms: AAV2

    Purification

    Protein A Affinity Chromatography

    Immunogène

    Recombinant AAV-2 Rep 78 protein, N-terminally truncated by 171 aa

    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

    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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