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DFNB31 antibody (Center)

DFNB31 Reactivity: Human WB, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2797202
  • Target See all DFNB31 Antibodies
    DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
    Binding Specificity
    • 7
    • 7
    • 7
    • 6
    • 3
    • 1
    • 1
    • 1
    • 1
    AA 378-406, Center
    Reactivity
    • 28
    • 3
    Human
    Host
    • 26
    • 4
    Rabbit
    Clonality
    • 27
    • 3
    Polyclonal
    Conjugate
    • 13
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This DFNB31 antibody is un-conjugated
    Application
    • 23
    • 18
    • 14
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Purpose
    Rabbit Anti-Human DFNB31 (Center) Antibody
    Immunogen
    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 Primary Antibody
  • Application Notes
    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
    Storage
    4 °C,-20 °C
    Storage Comment
    2-8°C (short-term), -20°C (long-term)
  • Target
    DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
    Alternative Name
    DFNB31 (DFNB31 Products)
    Synonyms
    DFNB31 antibody, CIP98 antibody, PDZD7B antibody, USH2D antibody, WHRN antibody, WI antibody, Cip98 antibody, Whrn antibody, 1110035G07Rik antibody, AW122018 antibody, AW742671 antibody, C430046P22Rik antibody, Dfnb31 antibody, wi antibody, whirlin antibody, WHRN antibody, LOC100555508 antibody, Whrn antibody
    Background

    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

    Molecular Weight
    96586 Da
    Gene ID
    25861
    UniProt
    Q9P202
    Pathways
    Sensory Perception of Sound
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