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EVC2 anticorps

EVC2 Reactivité: Humain, Souris ELISA, IHC, WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7243292
  • Antigène Voir toutes EVC2 Anticorps
    EVC2 (Ellis Van Creveld Syndrome 2 (EVC2))
    Reactivité
    Humain, Souris
    Hôte
    • 14
    • 1
    Lapin
    Clonalité
    • 15
    Polyclonal
    Conjugué
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp EVC2 est non-conjugé
    Application
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC), Western Blotting (WB)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Synthetic peptide of human EVC2
    Isotype
    IgG
    Top Product
    Discover our top product EVC2 Anticorps primaire
  • Indications d'application
    WB 1:200-1:1000, IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.5 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    EVC2 (Ellis Van Creveld Syndrome 2 (EVC2))
    Autre désignation
    EVC2 (EVC2 Produits)
    Synonymes
    anticorps EVC2, anticorps LBN, anticorps 1110017L09Rik, anticorps Lbn, anticorps limbin, anticorps EvC ciliary complex subunit 2, anticorps EVC2, anticorps Evc2
    Sujet
    This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants.
    Poids moléculaire
    148 kDa
    NCBI Accession
    NP_667338
    UniProt
    Q86UK5
    Pathways
    Signalisation Hedgehog
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