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DFNB31 Antikörper

DFNB31 Reaktivität: Human, Maus WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN5964388
  • Target Alle DFNB31 Antikörper anzeigen
    DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
    Reaktivität
    Human, Maus
    Wirt
    • 26
    • 4
    Kaninchen
    Klonalität
    • 27
    • 3
    Polyklonal
    Konjugat
    • 13
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser DFNB31 Antikörper ist unkonjugiert
    Applikation
    • 23
    • 18
    • 14
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant protein of human WHRN
    Isotyp
    IgG
    Top Product
    Discover our top product DFNB31 Primärantikörper
  • Applikationshinweise
    WB 1:500 - 1:2000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    1 mg/mL
    Buffer
    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
    Andere Bezeichnung
    WHRN (DFNB31 Produkte)
    Synonyme
    DFNB31 antikoerper, CIP98 antikoerper, PDZD7B antikoerper, USH2D antikoerper, WHRN antikoerper, WI antikoerper, Cip98 antikoerper, Whrn antikoerper, 1110035G07Rik antikoerper, AW122018 antikoerper, AW742671 antikoerper, C430046P22Rik antikoerper, Dfnb31 antikoerper, wi antikoerper, whirlin antikoerper, WHRN antikoerper, LOC100555508 antikoerper, Whrn antikoerper
    Hintergrund

    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.

    Molekulargewicht

    Observed_MW: 110kDa

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

    Gen-ID
    25861
    UniProt
    Q9P202
    Pathways
    Sensory Perception of Sound
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