Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

NDE1 anticorps

NDE1 Reactivité: Humain, Souris, Rat IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7011586
  • Antigène Voir toutes NDE1 Anticorps
    NDE1
    Reactivité
    • 19
    • 5
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 16
    • 3
    Lapin
    Clonalité
    • 16
    • 3
    Polyclonal
    Conjugué
    • 14
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp NDE1 est non-conjugé
    Application
    • 17
    • 13
    • 4
    • 4
    • 2
    • 1
    • 1
    Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human NDE1 (NP_060138.1).
    Isotype
    IgG
    Top Product
    Discover our top product NDE1 Anticorps primaire
  • Indications d'application
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 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.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    NDE1
    Autre désignation
    NDE1 (NDE1 Produits)
    Synonymes
    anticorps 2810027M15Rik, anticorps AU042936, anticorps AW822251, anticorps Nude, anticorps mNudE, anticorps HOM-TES-87, anticorps LIS4, anticorps NDE, anticorps NUDE, anticorps NUDE1, anticorps fb82g01, anticorps im:7141877, anticorps wu:fb82g01, anticorps zgc:114109, anticorps nudE neurodevelopment protein 1, anticorps Nde1, anticorps NDE1, anticorps nde1
    Sujet
    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.
    ID gène
    54820
    UniProt
    Q9NXR1
Vous êtes ici:
Support technique