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Corneodesmosin Antikörper (AA 100-200)

CDSN Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7266503
  • Target Alle Corneodesmosin (CDSN) Antikörper anzeigen
    Corneodesmosin (CDSN)
    Bindungsspezifität
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 100-200
    Reaktivität
    • 19
    • 3
    • 1
    Human
    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)
    Verwendungszweck
    CDSN Rabbit pAb
    Sequenz
    GGSAGSFKPG TGYSQVSYSS GSGSSLQGAS GSSQLGSSSS HSGSSGSHSG SSSSHSSSSS SFQFSSSSFQ VGNGSALPTN DNSYRGILNP SQPGQSSSSS Q
    Kreuzreaktivität
    Human, Maus, Ratte
    Produktmerkmale
    Polyclonal Antibodies
    Aufreinigung
    Affinity purification
    Immunogen
    A synthetic peptide corresponding to a sequence within amino acids 100-200 of human CDSN (NP_001255.3).
    Isotyp
    IgG
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  • Applikationshinweise
    WB,1:500 - 1:2000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    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
    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.,CDSN,HTSS,HTSS1,HYPT2,PSS,PSS1,S,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,CDSN
    Molekulargewicht
    51kDa
    Gen-ID
    1041
    UniProt
    Q15517
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