Espin 抗体 (AA 143-854)
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北京 101111
Quick Overview for Espin 抗体 (AA 143-854) (ABIN7870704)
抗原
See all Espin (ESPN) 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 143-854
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原理
- ESPN Antibody / Espin
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纯化方法
- Immunogen affinity purified
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免疫原
- E.coli-derived human ESPN recombinant protein (Position: H143-Y854) was used as the immunogen for the ESPN antibody.
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亚型
- IgG
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应用备注
- Optimal dilution of the ESPN antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL
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缓冲液
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
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储存条件
- 4 °C,-20 °C
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储存方法
- After reconstitution, the ESPN antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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- Espin (ESPN)
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别名
- ESPN
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背景
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ESPN antibody detects Espin, an actin-binding protein essential for the assembly and maintenance of parallel actin bundles in sensory cells, particularly in the stereocilia of hair cells in the inner ear. ESPN is required for hearing and balance by supporting the structural integrity of mechanosensory projections. The ESPN antibody is widely used in auditory biology, cytoskeletal, and sensory neuroscience research to study actin organization, hair cell morphology, and mechanotransduction.
ESPN is encoded by the ESPN gene located on human chromosome 1p36.31. The protein exists in multiple isoforms ranging from 1,000 to 1,100 amino acids, each containing actin-binding and proline-rich domains that mediate crosslinking of actin filaments. ESPN localizes to microvillar and stereociliary actin cores, where it provides structural reinforcement and length regulation.
The ESPN antibody detects bands between 90 and 110 kilodaltons depending on isoform and shows intense labeling of stereocilia and microvilli under immunofluorescence microscopy. ESPN promotes actin bundle stability by counteracting depolymerizing factors such as cofilin, ensuring the long-term maintenance of hair cell stereocilia. Its overexpression induces elongation of actin protrusions, while loss of function causes disorganization and degeneration of stereocilia, leading to deafness.
Mutations in ESPN are responsible for autosomal recessive deafness and vestibular dysfunction in both humans and animal models. Beyond auditory tissue, ESPN contributes to brush border maintenance in epithelial cells and to filopodia dynamics in neurons and immune cells, reflecting its broad cytoskeletal role.
Because of its crucial function in actin filament assembly and mechanosensory integrity, ESPN serves as a vital biomarker for studies of hearing, balance, and cytoskeletal structure. NSJ Bioreagents provides a validated ESPN antibody optimized for its applications, supporting investigations into actin regulation, auditory biology, and cellular architecture. -
UniProt
- B1AK53
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途径
- Sensory Perception of Sound
抗原
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