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DFNB31 anticorps (Middle Region)

Cet anticorps anti-DFNB31 est un anticorps Lapin Polyclonal détectant DFNB31 dans WB, IHC (p) et EIA. Adapté pour Humain.
N° du produit ABIN955575

Aperçu rapide pour DFNB31 anticorps (Middle Region) (ABIN955575)

Antigène

Voir toutes DFNB31 Anticorps
DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))

Reactivité

  • 23
  • 3
Humain

Hôte

  • 20
  • 4
Lapin

Clonalité

  • 21
  • 3
Polyclonal

Conjugué

  • 12
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp DFNB31 est non-conjugé

Application

  • 17
  • 13
  • 9
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
  • Épitope

    • 7
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 385-413, Middle Region

    Specificité

    This antibody recognizes Human Whirlin (Center).

    Purification

    Affinity Chromatography on Protein A

    Immunogène

    KLH conjugated synthetic peptide between 385-413 amino acids from the Central region of Human Whirlin. Genename: WHRN

    Isotype

    Ig Fraction
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS, 0.09 % Sodium Azide

    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.

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Antigène

    DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))

    Autre désignation

    Whirlin

    Sujet

    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.Synonyms: Autosomal recessive deafness type 31 protein, DFNB31, KIAA1526, WHRN

    Poids moléculaire

    96586 Da

    ID gène

    25861

    NCBI Accession

    NP_001077354

    Pathways

    Sensory Perception of Sound
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