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Mouse Anti-ESPN Recombinant Antibody (CBFYE-1237) (CBMAB-E1808-FY)

This product is mouse antibody that recognizes ESPN. The antibody CBFYE-1237 can be used for immunoassay techniques such as: WB, IP, IF, ELISA.
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Summary

Host Animal
Mouse
Specificity
Mouse, Rat, Human
Clone
CBFYE-1237
Application
WB, IP, IF, ELISA

Basic Information

Specificity
Mouse, Rat, Human
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Concentration
0.2 mg/mL
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
Espin
Introduction
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.
Entrez Gene ID
Human83715
Mouse56226
Rat56227
UniProt ID
HumanB1AK53
MouseQ9ET47
RatQ63618
Alternative Names
Espin; Autosomal Recessive Deafness Type 36 Protein; Ectoplasmic Specialization Protein; DFNB36; Deafness, Autosomal Recessive 36; LP2654
Research Area
Multifunctional actin-bundling protein. Plays a major role in regulating the organization, dimension, dynamics and signaling capacities of the actin filament-rich microvilli in the mechanosensory and chemosensory cells (PubMed:29572253).

Required for the assembly and stabilization of the stereociliary parallel actin bundles. Plays a crucial role in the formation and maintenance of inner ear hair cell stereocilia (By similarity).

Involved in the elongation of actin in stereocilia (PubMed:29572253).

In extrastriolar hair cells, required for targeting MYO3B to stereocilia tips, and for regulation of stereocilia diameter and staircase formation.
Biological Process
Actin filament bundle assembly Source: GO_Central
Microvillar actin bundle assembly Source: UniProtKB
Sensory perception of sound Source: UniProtKB-KW
Cellular Location
Cytoskeleton; Stereocilium; Microvillus
Involvement in disease
Deafness, autosomal recessive, 36, with or without vestibular involvement (DFNB36):
A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. DFNB36 is characterized by prelingual, profound hearing loss, and vestibular areflexia in some patients.
Usher syndrome 1M (USH1M):
A form of Usher syndrome, a genetically heterogeneous condition characterized by the association of retinitis pigmentosa with sensorineural deafness. Age at onset and differences in auditory and vestibular function distinguish Usher syndrome type 1 (USH1), Usher syndrome type 2 (USH2) and Usher syndrome type 3 (USH3). USH1M is an autosomal recessive disease characterized by prelingual sensorineural hearing loss, vestibular dysfunction, night blindness, and progressive impairment of vision.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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