DFNB31 anticorps (AA 378-406)

N° du produit ABIN655065

Détail du produit anti-DFNB31 anticorps

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

Épitope: AA 378-406

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DFNB31 est non-conjugé

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

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: 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.

Clone: RB19059

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. IHC-P: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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.

Stock: 4 °C,-20 °C

Stockage commentaire: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Détails sur DFNB31

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

Autre désignation: DFNB31 (DFNB31 Produits)

Synonymes: anticorps DFNB31, anticorps CIP98, anticorps PDZD7B, anticorps USH2D, anticorps WHRN, anticorps WI, anticorps Cip98, anticorps Whrn, anticorps 1110035G07Rik, anticorps AW122018, anticorps AW742671, anticorps C430046P22Rik, anticorps Dfnb31, anticorps wi, anticorps whirlin, anticorps WHRN, anticorps LOC100555508, anticorps Whrn

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.

Poids moléculaire: 96558

ID gène: 25861

NCBI Accession: NP_001077354, NP_001166896, NP_056219

UniProt: Q9P202

Pathways: Sensory Perception of Sound