DFNB31 anticorps (Middle Region)

N° du produit ABIN955575

Détail du produit anti-DFNB31 anticorps

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

Épitope: AA 385-413, Middle Region

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)

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 (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.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