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Cullin 3 anticorps

CUL3 Reactivité: Humain, Souris, Rat IHC, IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7255411
  • Antigène Voir toutes Cullin 3 (CUL3) Anticorps
    Cullin 3 (CUL3)
    Reactivité
    • 52
    • 23
    • 18
    • 6
    • 6
    • 5
    • 4
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    Humain, Souris, Rat
    Hôte
    • 49
    • 2
    • 1
    Lapin
    Clonalité
    • 46
    • 6
    Polyclonal
    Conjugué
    • 31
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Cullin 3 est non-conjugé
    Application
    • 24
    • 16
    • 14
    • 13
    • 13
    • 7
    • 5
    • 5
    • 3
    • 1
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human CUL3 (NP_003581.1).
    Isotype
    IgG
    Top Product
    Discover our top product CUL3 Anticorps primaire
  • Indications d'application
    IHC 1:50-1:100 IF 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
    Cullin 3 (CUL3)
    Autre désignation
    CUL3 (CUL3 Produits)
    Sujet
    This gene encodes a member of the cullin protein family. The encoded protein plays a critical role in the polyubiquitination and subsequent degradation of specific protein substrates as the core component and scaffold protein of an E3 ubiquitin ligase complex. Complexes including the encoded protein may also play a role in late endosome maturation. Mutations in this gene are a cause of type 2E pseudohypoaldosteronism. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
    ID gène
    8452
    UniProt
    Q13618
    Pathways
    M Phase
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