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Rabbit anti-Human CDSN Polyclonal Antibody

The antibody against CDSN was raised in rabbit using the Human CDSN as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.

ADC-53822A

The antibody against CDSN was raised in rabbit using the Human CDSN as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.

$600.00

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Specifications


Cat.No ADC-53822A ClonalityPolyclonal
Host SpeciesRabbitTarget NameCDSN
FormLiquidSpecies ReactivityHuman, Mouse
IsotypeIgGStorage Buffer50% Glycerol, Avoid freeze / thaw cycles., PBS with 0.02% sodium azide
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHCStorageUpon receipt

Immunogen Information


Immunogen DescriptionHuman CDSNTarget SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ15517
Background Information
  • Uniprot Id

    Q15517

  • Target Species

    Human

  • Target Name

    CDSN

  • Target Full Name

    Corneodesmosin

  • Target Function

    Important for the epidermal barrier integrity.

  • Target Involvement

    Hypotrichosis 2 (HYPT2); Peeling skin syndrome 1 (PSS1)

  • Target Subcellular Location

    Secreted. Note=Found in corneodesmosomes, the intercellular structures that are involved in desquamation.

  • Target Tissue Specificity

    Exclusively expressed in skin.

  • Target Synonyms

    AI747712; CDSN; CDSN_HUMAN; Corneodesmosin; D6S586E; DADB-141O4.5; Differentiated keratinocyte S protein; HTSS; S; S protein

  • Target 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.

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