Espin anticorps (AA 143-854)

N° du produit ABIN7600060

Cet anticorps anti-Espin est un anticorps Lapin Polyclonal détectant Espin dans WB et ELISA. Adapté pour Souris et Rat.

Aperçu rapide pour Espin anticorps (AA 143-854) (ABIN7600060)

Antigène: Espin (ESPN)

Reactivité: Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Espin est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-Espin anticorps

Épitope: AA 143-854

Fonction: Anti-ESPN Antibody

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

Attributs du produit: Anti-ESPN Antibody (ABIN7600060). Tested in WB, ELISA applications. This antibody reacts with Mouse, Rat. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

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: Western blot, 0.25-0.5 μg/mL, Mouse, Rat
ELISA, 0.1-0.5 μg/mL

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Détails sur Espin

Antigène: Espin (ESPN)

Autre désignation: ESPN

Sujet:

Synonyms: ESPN, DFNB36, LP2654, Espin, Autosomal recessive deafness type 36 protein, Ectoplasmic specialization protein

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.

Poids moléculaire: 110 kDa

ID gène: 83715

Pathways: Sensory Perception of Sound