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EVC2 Antikörper

EVC2 Reaktivität: Human, Maus ELISA, IHC, WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7243292
  • Target Alle EVC2 Antikörper anzeigen
    EVC2 (Ellis Van Creveld Syndrome 2 (EVC2))
    Reaktivität
    Human, Maus
    Wirt
    • 14
    • 1
    Kaninchen
    Klonalität
    • 15
    Polyklonal
    Konjugat
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser EVC2 Antikörper ist unkonjugiert
    Applikation
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC), Western Blotting (WB)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Synthetic peptide of human EVC2
    Isotyp
    IgG
    Top Product
    Discover our top product EVC2 Primärantikörper
  • Applikationshinweise
    WB 1:200-1:1000, IHC 1:50-1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1.5 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    EVC2 (Ellis Van Creveld Syndrome 2 (EVC2))
    Andere Bezeichnung
    EVC2 (EVC2 Produkte)
    Synonyme
    EVC2 antikoerper, LBN antikoerper, 1110017L09Rik antikoerper, Lbn antikoerper, limbin antikoerper, EvC ciliary complex subunit 2 antikoerper, EVC2 antikoerper, Evc2 antikoerper
    Hintergrund
    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.
    Molekulargewicht
    148 kDa
    NCBI Accession
    NP_667338
    UniProt
    Q86UK5
    Pathways
    Hedgehog Signalweg
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