USH1G anticorps

N° du produit ABIN7120659

Cet anticorps anti-USH1G est un anticorps Lapin Polyclonal détectant USH1G dans ELISA et IP. Adapté pour Humain.

Aperçu rapide pour USH1G anticorps (ABIN7120659)

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)

Détail du produit anti-USH1G anticorps

Fonction: USH1G antibody

Purification: Immunogen affinity purified

Pureté: ≥95 % as determined by SDS-PAGE

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

Format: Liquid

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

Stockage commentaire: -20°C for 12 months

Date de péremption: 12 months

Détails sur USH1G

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

Autre désignation: USH1G

Sujet:

Synonyms: pre-mRNA splicing regulator USH1G|Scaffold protein containing ankyrin repeats and SAM domain|Usher syndrome type-1G protein|USH1G|SANS

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: 52 kDa

ID gène: 124590

UniProt: Q495M9

Pathways: Sensory Perception of Sound