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Corneodesmosin antibody (AA 100-200)

The Rabbit Polyclonal anti-Corneodesmosin antibody has been validated for WB. It is suitable to detect Corneodesmosin in samples from Human.
Catalog No. ABIN7266503

Quick Overview for Corneodesmosin antibody (AA 100-200) (ABIN7266503)

Target

See all Corneodesmosin (CDSN) Antibodies
Corneodesmosin (CDSN)

Reactivity

  • 22
  • 3
  • 1
Human

Host

  • 14
  • 4
  • 3
  • 1
Rabbit

Clonality

  • 19
  • 3
Polyclonal

Conjugate

  • 17
  • 2
  • 2
  • 1
This Corneodesmosin antibody is un-conjugated

Application

  • 16
  • 13
  • 11
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 7
    • 2
    • 2
    • 2
    • 1
    • 1
    AA 100-200

    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
  • 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

    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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