Espin anticorps (AA 143-854) (Fluoro488)

N° du produit ABIN7988459

Cet anticorps anti-Espin Polyclonal Lapin conjugué à Fluoro488 (ABIN7988459) détecte spécifiquement Espin dans FACS. L’anticorps est réactif avec des échantillons de Souris et Rat.

Aperçu rapide pour Espin anticorps (AA 143-854) (Fluoro488) (ABIN7988459)

Antigène: Espin (ESPN)

Reactivité: Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Espin est conjugé à/à la Fluoro488

Application: Flow Cytometry (FACS)

Détail du produit anti-Espin anticorps (Fluoro488)

Épitope: AA 143-854

Fonction: Anti-ESPN Antibody Fluoro488 Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins

Homologie: Human ESPN shares 75.6%,78.1% amino acid (aa) sequence identity with mouse,rat ESPN,respectively.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human ESPN recombinant protein (Position: H143-Y854). Human ESPN shares 75.6% and 78.1% amino acid (aa) sequence identity with mouse and rat ESPN, respectively.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % 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: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur Espin

Antigène: Espin (ESPN)

Autre désignation: ESPN

Sujet:

Background: This gene encodes a multifunctional actin-bundling protein. It plays a major role in regulating the organization, dimensions, dynamics, and signaling capacities of the actin filament-rich, microvillus-type specializations that mediate sensory transduction in various mechanosensory and chemosensory cells. Mutations in this gene are associated with autosomal recessive neurosensory deafness, and autosomal dominant sensorineural deafness without vestibular involvement.

Gene Full Name: espin

ID gène: 83715

UniProt: B1AK53

Pathways: Sensory Perception of Sound