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DFNB31 anticorps

DFNB31 Reactivité: Humain, Souris WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6567020
  • Antigène Voir toutes DFNB31 Anticorps
    DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
    Reactivité
    Humain, Souris
    Hôte
    • 24
    • 4
    Lapin
    Clonalité
    • 25
    • 3
    Polyclonal
    Conjugué
    • 11
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp DFNB31 est non-conjugé
    Application
    • 21
    • 18
    • 14
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human WHRN
    Isotype
    IgG
    Top Product
    Discover our top product DFNB31 Anticorps primaire
  • Indications d'application
    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.
    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
    DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
    Autre désignation
    WHRN (DFNB31 Produits)
    Synonymes
    anticorps DFNB31, anticorps CIP98, anticorps PDZD7B, anticorps USH2D, anticorps WHRN, anticorps WI, anticorps Cip98, anticorps Whrn, anticorps 1110035G07Rik, anticorps AW122018, anticorps AW742671, anticorps C430046P22Rik, anticorps Dfnb31, anticorps wi, anticorps whirlin, anticorps WHRN, anticorps LOC100555508, anticorps Whrn
    Sujet

    Synonyms: Whirlin,Autosomal Recessive Deafness Type 31 Protein,DFNB31,Deafness Autosomal Recessive 31,CASK-Interacting Protein CIP98,KIAA1526,PDZD7B,CIP98,USH2D,WI,WHRN,KIAA1526

    Background: This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing results in multiple transcript variants.

    Poids moléculaire

    Observed_MW: 110kDa

    Calculated_MW: 37kDa/55kDa/59kDa/96kDa

    ID gène
    25861
    UniProt
    Q9P202
    Pathways
    Sensory Perception of Sound
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