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Corneodesmosin anticorps (AA 100-200)

CDSN Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7266503
  • Antigène Voir toutes Corneodesmosin (CDSN) Anticorps
    Corneodesmosin (CDSN)
    Épitope
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 100-200
    Reactivité
    • 19
    • 3
    • 1
    Humain
    Hôte
    • 12
    • 3
    • 3
    • 1
    Lapin
    Clonalité
    • 17
    • 2
    Polyclonal
    Conjugué
    • 14
    • 2
    • 2
    • 1
    Cet anticorp Corneodesmosin est non-conjugé
    Application
    • 13
    • 12
    • 8
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Fonction
    CDSN Rabbit pAb
    Séquence
    GGSAGSFKPG TGYSQVSYSS GSGSSLQGAS GSSQLGSSSS HSGSSGSHSG SSSSHSSSSS SFQFSSSSFQ VGNGSALPTN DNSYRGILNP SQPGQSSSSS Q
     Réactivité croisée
    Humain, Souris, Rat
    Attributs du produit
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogène
    A synthetic peptide corresponding to a sequence within amino acids 100-200 of human CDSN (NP_001255.3).
    Isotype
    IgG
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    Discover our top product CDSN Anticorps primaire
  • Indications d'application
    WB,1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    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
    Corneodesmosin (CDSN)
    Autre désignation
    CDSN (CDSN Produits)
    Synonymes
    anticorps D6S586E, anticorps HTSS, anticorps HTSS1, anticorps PSS, anticorps S, anticorps AI747712, anticorps corneodesmosin, anticorps CDSN, anticorps Cdsn
    Sujet
    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
    Poids moléculaire
    51kDa
    ID gène
    1041
    UniProt
    Q15517
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