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CDH23 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement CDH23 dans WB, ELISA et IHC. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN7112149

Aperçu rapide pour CDH23 anticorps (ABIN7112149)

Antigène

Voir toutes CDH23 Anticorps
CDH23 (Cadherin 23 (CDH23))

Reactivité

  • 45
  • 24
  • 17
  • 3
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 43
  • 1
  • 1
Lapin

Clonalité

  • 45
Polyclonal

Conjugué

  • 17
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp CDH23 est non-conjugé

Application

  • 13
  • 13
  • 12
  • 10
  • 7
  • 7
  • 6
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Fonction

    CDH23 antibody

    Purification

    Immunogen affinity purified

    Pureté

    ≥95 % as determined by SDS-PAGE

    Immunogène

    cadherin-like 23

    Isotype

    IgG
  • Indications d'application

    WB: 1:500 - 1:2000, IHC: 1:100 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 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.

    Conseil sur la manipulation

    Avoid repeated freeze / thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    -20°C for 12 months

    Date de péremption

    12 months
  • Antigène

    CDH23 (Cadherin 23 (CDH23))

    Autre désignation

    CDH23

    Sujet

    Synonyms: Cadherin-23|Otocadherin|CDH23|KIAA1774|KIAA1812

    Background: This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Upregulation of this gene may also be associated with breast cancer. Alternative splice variants encoding different isoforms have been described.

    Poids moléculaire

    59 kDa

    ID gène

    64072

    UniProt

    Q9H251

    Pathways

    Sensory Perception of Sound
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