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Corneodesmosin antibody (AA 100-200)

CDSN Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7266503
  • Target See all Corneodesmosin (CDSN) Antibodies
    Corneodesmosin (CDSN)
    Binding Specificity
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 100-200
    Reactivity
    • 19
    • 3
    • 1
    Human
    Host
    • 12
    • 3
    • 3
    • 1
    Rabbit
    Clonality
    • 17
    • 2
    Polyclonal
    Conjugate
    • 14
    • 2
    • 2
    • 1
    This Corneodesmosin antibody is un-conjugated
    Application
    • 13
    • 12
    • 8
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Purpose
    CDSN Rabbit pAb
    Sequence
    GGSAGSFKPG TGYSQVSYSS GSGSSLQGAS GSSQLGSSSS HSGSSGSHSG SSSSHSSSSS SFQFSSSSFQ VGNGSALPTN DNSYRGILNP SQPGQSSSSS Q
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    A synthetic peptide corresponding to a sequence within amino acids 100-200 of human CDSN (NP_001255.3).
    Isotype
    IgG
    Top Product
    Discover our top product CDSN Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Corneodesmosin (CDSN)
    Alternative Name
    CDSN (CDSN Products)
    Synonyms
    D6S586E antibody, HTSS antibody, HTSS1 antibody, PSS antibody, S antibody, AI747712 antibody, corneodesmosin antibody, CDSN antibody, Cdsn antibody
    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.,CDSN,HTSS,HTSS1,HYPT2,PSS,PSS1,S,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,CDSN
    Molecular Weight
    51kDa
    Gene ID
    1041
    UniProt
    Q15517
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