Espin antibody (AA 143-854)

Catalog No. ABIN7600060

This anti-Espin antibody is a Rabbit Polyclonal antibody detecting Espin in WB and ELISA. Suitable for Mouse and Rat.

Quick Overview for Espin antibody (AA 143-854) (ABIN7600060)

Target: Espin (ESPN)

Reactivity: Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Espin antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-Espin Antibody

Binding Specificity: AA 143-854

Purpose: Anti-ESPN Antibody

Cross-Reactivity (Details): No cross-reactivity with other proteins

Characteristics: 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.

Immunogen: 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

Application Details

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

Restrictions: For Research Use only

Handling

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.

Storage: 4 °C,-20 °C

Storage Comment: 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.

Target Details for Espin

Target: Espin (ESPN)

Alternative Name: ESPN

Background:

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.

Molecular Weight: 110 kDa

Gene ID: 83715

Pathways: Sensory Perception of Sound