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DFNB31 anticorps (Center)

DFNB31 Reactivité: Humain WB, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN2797202
  • Antigène Voir toutes DFNB31 Anticorps
    DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
    Épitope
    • 7
    • 7
    • 7
    • 6
    • 3
    • 1
    • 1
    • 1
    • 1
    AA 378-406, Center
    Reactivité
    • 28
    • 3
    Humain
    Hôte
    • 26
    • 4
    Lapin
    Clonalité
    • 27
    • 3
    Polyclonal
    Conjugué
    • 13
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp DFNB31 est non-conjugé
    Application
    • 23
    • 18
    • 14
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Fonction
    Rabbit Anti-Human DFNB31 (Center) Antibody
    Immunogène
    This DFNB31 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 378-406 amino acids from the Central region of human DFNB31.
    Isotype
    Ig Fraction
    Top Product
    Discover our top product DFNB31 Anticorps primaire
  • Indications d'application
    Western Blot, Immunohistochemistry
    Recommended Dilutions
    WB: 1:1000, IHC: 1:10-50Western blot analysis of lysate from human kidney tissue lysate, using DFNB31 Antibody (Center) for immunohistochemistry. Clinical relevance has not been evaluated.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/mL
    Stock
    4 °C,-20 °C
    Stockage commentaire
    2-8°C (short-term), -20°C (long-term)
  • Antigène
    DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
    Autre désignation
    DFNB31 (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

    Target Description: 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 of this gene results in multiple transcript variants encoding different isoforms.

    Gene Symbol: DFNB31

    Poids moléculaire
    96586 Da
    ID gène
    25861
    UniProt
    Q9P202
    Pathways
    Sensory Perception of Sound
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