DFNB31 anticorps (Middle Region)

N° du produit ABIN955575

Cet anticorps anti-DFNB31 Polyclonal Lapin (ABIN955575) détecte spécifiquement DFNB31 dans WB, IHC (p) et EIA. L’anticorps est réactif avec des échantillons de Humain.

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

Antigène: DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DFNB31 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Détail du produit anti-DFNB31 anticorps

Épitope: 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

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

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.

Détails sur DFNB31

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