Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Corneodesmosin antibody

CDSN Reactivity: Human, Mouse, Rat WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6568410
  • Target See all Corneodesmosin (CDSN) Antibodies
    Corneodesmosin (CDSN)
    Reactivity
    Human, Mouse, Rat
    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)
    Purification
    Affinity purification
    Immunogen
    A synthetic peptide of human CDSN
    Isotype
    IgG
    Top Product
    Discover our top product CDSN Primary Antibody
  • Application Notes
    WB 1:500 - 1:2000
    Restrictions
    For Research Use only
  • Concentration
    1 mg/mL
    Buffer
    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

    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.

    Molecular Weight

    Observed_MW: 48kDa

    Calculated_MW: 51kDa

    Gene ID
    1041
    UniProt
    Q15517
You are here:
Support