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Doublecortin 抗体 (AA 74-100)

This anti-Doublecortin antibody is a 兔 多克隆 antibody detecting Doublecortin in WB. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN5708336
发货至: 中国

Quick Overview for Doublecortin 抗体 (AA 74-100) (ABIN5708336)

抗原

See all Doublecortin (DCX) 抗体
Doublecortin (DCX)

适用

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人, 小鼠, 大鼠

宿主

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克隆类型

  • 91
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多克隆

标记

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This Doublecortin antibody is un-conjugated

应用范围

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Western Blotting (WB)
  • 抗原表位

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    AA 74-100

    纯化方法

    Antigen affinity purified

    免疫原

    Amino acids 74-100 (QSLRFHQNMELDFGHFDERDKTSRNMR-human) were used as the immunogen for the DCX antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the DCX antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL

    限制

    仅限研究用
  • 缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    -20 °C

    储存方法

    After reconstitution, the DCX antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • 抗原

    Doublecortin (DCX)

    别名

    Doublecortin / DBCN / DCX

    背景

    Neuronal migration protein Doublecortin, also known as Doublin or Lissencephalin-X, is a protein that in humans is encoded by the DCX gene. This gene encodes a member of the doublecortin family. The protein encoded by this gene is a cytoplasmic protein and contains two doublecortin domains, which bind microtubules. In the developing cortex, cortical neurons must migrate over long distances to reach the site of their final differentiation. The encoded protein appears to direct neuronal migration by regulating the organization and stability of microtubules. In addition, the encoded protein interacts with LIS1, the regulatory gamma subunit of platelet activating factor acetylhydrolase, and this interaction is important to proper microtubule function in the developing cortex. Mutations in this gene cause abnormal migration of neurons during development and disrupt the layering of the cortex, leading to epilepsy, mental retardation, subcortical band heterotopia (double cortex syndrome) in females and lissencephaly (smooth brain syndrome) in males. Multiple transcript variants encoding different isoforms have been found for this gene.

    UniProt

    O43602
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