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Doublecortin Protein (DCX) (Transcript Variant 2) (Myc-DYKDDDDK Tag)

This Recombinant Doublecortin protein is expressed in HEK-293 Cells.
产品编号 ABIN2719682
发货至: 中国
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Quick Overview for Doublecortin Protein (DCX) (Transcript Variant 2) (Myc-DYKDDDDK Tag) (ABIN2719682)

抗原

See all Doublecortin (DCX) 蛋白
Doublecortin (DCX)

蛋白类型

Recombinant

宿主

  • 10
  • 3
  • 2
  • 2

资源

  • 7
  • 5
  • 2
  • 1
  • 1
  • 1
HEK-293 Cells

应用范围

Antibody Production (AbP), Standard (STD)

纯度

> 80 % as determined by SDS-PAGE and Coomassie blue staining
  • 产品特性

    Transcript Variant 2

    标记

    This Doublecortin protein is labelled with Myc-DYKDDDDK Tag.

    产品特性

    • Recombinant human Doublecortin (transcript variant 2) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
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    Product
    表达系统
    Conjugate
    Origin
    价格从
    表达系统 HEK-293 Cells
    Conjugate His tag
    Origin Human
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    Conjugate Strep Tag
    Origin Human
    价格从 145,985.55 ¥

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  • 应用备注

    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays

    说明

    The tag is located at the C-terminal.

    限制

    仅限研究用
  • 浓度

    50 μg/mL

    缓冲液

    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

    储存条件

    -80 °C

    储存方法

    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • 抗原

    Doublecortin (DCX)

    别名

    Doublecortin

    背景

    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.

    分子量

    40.4 kDa

    NCBI登录号

    NP_835365
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