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NDE1 anticorps (AA 74-335)

Cet anticorps anti-NDE1 Polyclonal Lapin (ABIN7876714) détecte spécifiquement NDE1 dans WB, ELISA, IHC (p) et FACS. L’anticorps est réactif avec des échantillons de Humain.
N° du produit ABIN7876714
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour NDE1 anticorps (AA 74-335) (ABIN7876714)

Antigène

Voir toutes NDE1 Anticorps
NDE1

Reactivité

  • 18
  • 6
  • 6
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 15
  • 3
Lapin

Clonalité

  • 15
  • 3
Polyclonal

Conjugué

  • 18
Cet anticorp NDE1 est non-conjugé

Application

  • 15
  • 11
  • 7
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Épitope

    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 74-335

    Fonction

    NDE1 Antibody / NudE

    Purification

    Affinity purified

    Immunogène

    An E. coli-derived human protein (amino acids E74-C335) was used as the immunogen for the NDE1 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the NDE1 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the NDE1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    NDE1

    Autre désignation

    NDE1

    Sujet

    Nuclear distribution protein nudE homolog 1 is a protein that in humans is encoded by the NDE1 gene. This gene encodes a member of the nuclear distribution E (NudE) family of proteins. The encoded protein is localized at the centrosome and interacts with other centrosome components as part of a multiprotein complex that regulates dynein function. This protein plays an essential role in microtubule organization, mitosis and neuronal migration. Mutations in this gene cause lissencephaly 4, a disorder characterized by lissencephaly, severe brain atrophy, microcephaly, and severe cognitive disability. Alternative splicing results in multiple transcript variants.

    UniProt

    Q9NXR1
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