DFNB31 anticorps (AA 378-406)

N° du produit ABIN5532540

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.

Isotype: Ig Fraction

Information d'application

Indications d'application: For WB starting dilution is: 1:1000

For IHC-P starting dilution is: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: 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: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

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: 97 kDa

ID gène: 25861

UniProt: Q9P202

Pathways: Sensory Perception of Sound