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COCH anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement COCH dans IHC et IF. Il présente une réactivité envers Humain.
N° du produit ABIN7262425

Aperçu rapide pour COCH anticorps (ABIN7262425)

Antigène

Voir toutes COCH Anticorps
COCH (Cochlin (COCH))

Reactivité

  • 39
  • 13
  • 5
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 37
  • 2
Lapin

Clonalité

  • 39
Polyclonal

Conjugué

  • 21
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp COCH est non-conjugé

Application

  • 29
  • 18
  • 11
  • 10
  • 2
  • 2
  • 2
Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human COCH (NP_001128530.1).

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:100 IF 1:50-1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 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.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    COCH (Cochlin (COCH))

    Autre désignation

    COCH

    Sujet

    The protein encoded by this gene is highly conserved in human, mouse, and chicken, showing 94 % and 79 % amino acid identity of human to mouse and chicken sequences, respectively. Hybridization to this gene was detected in spindle-shaped cells located along nerve fibers between the auditory ganglion and sensory epithelium. These cells accompany neurites at the habenula perforata, the opening through which neurites extend to innervate hair cells. This and the pattern of expression of this gene in chicken inner ear paralleled the histologic findings of acidophilic deposits, consistent with mucopolysaccharide ground substance, in temporal bones from DFNA9 (autosomal dominant nonsyndromic sensorineural deafness 9) patients. Mutations that cause DFNA9 have been reported in this gene. Alternative splicing results in multiple transcript variants encoding the same protein. Additional splice variants encoding distinct isoforms have been described but their biological validities have not been demonstrated.

    ID gène

    1690

    UniProt

    O43405

    Pathways

    Sensory Perception of Sound
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