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NDE1 anticorps

Cet anticorps anti-NDE1 est un anticorps Lapin Polyclonal détectant NDE1 dans WB, IHC, ELISA, IF et IP. Adapté pour Humain, Souris et Rat.
N° du produit ABIN5700144

Aperçu rapide pour NDE1 anticorps (ABIN5700144)

Antigène

Voir toutes NDE1 Anticorps
NDE1

Reactivité

  • 16
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 13
  • 3
Lapin

Clonalité

  • 13
  • 3
Polyclonal

Conjugué

  • 16
Cet anticorp NDE1 est non-conjugé

Application

  • 14
  • 9
  • 6
  • 4
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF), Immunoprecipitation (IP)
  • Fonction

    NDE1 antibody

    Immunogène

    nudE nuclear distribution gene E homolog 1 (A. nidulans)

    Isotype

    IgG
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Commentaires

    A2780 cells were subjected to SDS PAGE followed by western blot with FNab05600(NDE1 antibody) at dilution of 1:1500

    Restrictions

    For Research Use only
  • Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

    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.

    Conseil sur la manipulation

    Avoid repeated freeze / thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    -20°C for 12 months

    Date de péremption

    12 months
  • Antigène

    NDE1

    Autre désignation

    NDE1

    Sujet

    Synonyms: Nuclear distribution protein nudE homolog 1 (NudE)|NDE1|NUDE

    Background: 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 mental retardation. Alternative splicing results in multiple transcript variants.

    Poids moléculaire

    40 kDa

    ID gène

    54820

    UniProt

    Q9NXR1
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