USH1G anticorps

N° du produit ABIN5705181

Détail du produit anti-USH1G anticorps

Antigène: USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp USH1G est non-conjugé

Application: ELISA, Immunoprecipitation (IP)

Immunogène: Usher syndrome 1G (autosomal recessive)

Isotype: IgG

Information d'application

Indications d'application: IP:1:200-1:2000

Restrictions: For Research Use only

Stockage

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol  pH 7.3

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 freeze / thaw cycles.

Stock: -20 °C

Date de péremption: 12 months

Détails sur USH1G

Antigène: USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))

Autre désignation: USH1G (USH1G Produits)

Synonymes: anticorps ANKS4A, anticorps SANS, anticorps Sans, anticorps js, anticorps USH1 protein network component sans, anticorps USH1G, anticorps Ush1g

Sujet: Synonyms:ANKS4A, FLJ33924, SANS, USH1G, Usher syndrome type 1G protein Background:Required for normal development and maintenance of cochlear hair cell bundles. Anchoring/scaffolding protein that is a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransduction in cochlear hair cells. Required for normal hearing.

Poids moléculaire: 40kDa

ID gène: 124590

UniProt: Q495M9

Pathways: Sensory Perception of Sound