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Corneodesmosin Antikörper

CDSN Reaktivität: Human, Maus, Ratte WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN6568410
  • Target Alle Corneodesmosin (CDSN) Antikörper anzeigen
    Corneodesmosin (CDSN)
    Reaktivität
    Human, Maus, Ratte
    Wirt
    • 12
    • 3
    • 3
    • 1
    Kaninchen
    Klonalität
    • 17
    • 2
    Polyklonal
    Konjugat
    • 14
    • 2
    • 2
    • 1
    Dieser Corneodesmosin Antikörper ist unkonjugiert
    Applikation
    • 13
    • 12
    • 8
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Aufreinigung
    Affinity purification
    Immunogen
    A synthetic peptide of human CDSN
    Isotyp
    IgG
    Top Product
    Discover our top product CDSN Primärantikörper
  • Applikationshinweise
    WB 1:500 - 1:2000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    1 mg/mL
    Buffer
    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    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
    Corneodesmosin (CDSN)
    Andere Bezeichnung
    CDSN (CDSN Produkte)
    Synonyme
    D6S586E antikoerper, HTSS antikoerper, HTSS1 antikoerper, PSS antikoerper, S antikoerper, AI747712 antikoerper, corneodesmosin antikoerper, CDSN antikoerper, Cdsn antikoerper
    Hintergrund

    Synonyms: AI747712,CDSN,CDSN,Corneodesmosin,D6S586E,DADB-141O4.5,Differentiated keratinocyte S protein,HTSS,S,S protein

    Background: This gene encodes a protein found in corneodesmosomes, which localize to human epidermis and other cornified squamous epithelia. The encoded protein undergoes a series of cleavages during corneocyte maturation. This gene is highly polymorphic in human populations, and variation has been associated with skin diseases such as psoriasis, hypotrichosis and peeling skin syndrome. The gene is located in the major histocompatibility complex (MHC) class I region on chromosome 6.

    Molekulargewicht

    Observed_MW: 48kDa

    Calculated_MW: 51kDa

    Gen-ID
    1041
    UniProt
    Q15517
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