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Espin 抗体 (AA 143-854)

This 兔 多克隆 anti-Espin antibody specifically detects Espin in WB 和 ELISA. The antibody is reactive with 小鼠 和 大鼠 samples.
产品编号 ABIN7600060
发货至: 中国
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Quick Overview for Espin 抗体 (AA 143-854) (ABIN7600060)

抗原

See all Espin (ESPN) 抗体
Espin (ESPN)

适用

  • 21
  • 9
  • 9
小鼠, 大鼠

宿主

  • 21

克隆类型

  • 21
多克隆

标记

  • 9
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Espin antibody is un-conjugated

应用范围

  • 13
  • 10
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA
  • 抗原表位

    • 8
    • 3
    • 1
    AA 143-854

    原理

    Anti-ESPN Antibody

    交叉反应 (详细)

    No cross-reactivity with other proteins

    产品特性

    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.

    纯化方法

    Immunogen affinity purified.

    免疫原

    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.

    亚型

    IgG
  • 应用备注

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

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

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

    浓度

    500 μg/mL

    缓冲液

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

    储存条件

    4 °C,-20 °C

    储存方法

    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.
  • 抗原

    Espin (ESPN)

    别名

    ESPN

    背景

    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.

    分子量

    110 kDa

    基因ID

    83715

    途径

    Sensory Perception of Sound
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