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DFNB31 antibody

DFNB31 Reactivity: Human, Mouse WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6567020
$438.90
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  • Target See all DFNB31 Antibodies
    DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
    Reactivity
    Human, Mouse
    Host
    • 31
    • 4
    Rabbit
    Clonality
    • 32
    • 3
    Polyclonal
    Conjugate
    • 16
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This DFNB31 antibody is un-conjugated
    Application
    • 28
    • 20
    • 17
    • 3
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human WHRN
    Isotype
    IgG
  • Application Notes
    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.
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
    Alternative Name
    WHRN (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

    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.

    Molecular Weight

    Observed_MW: 110kDa

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

    Gene ID
    25861
    UniProt
    Q9P202
    Pathways
    Sensory Perception of Sound
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