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AC133-2分子的克隆及其逆转录病毒表达载体的构建 被引量:1

The Cloning of the AC133-2 and Construction of Its Retroviral Expressing Vector
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摘要 目的克隆人AC133-2全长基因,构建PGEZ-Term-AC133—2逆转录病毒表达载体。方法采用分段克隆的方法,通过聚合链式反应从胎肝文库中克隆AC133-2,并构建AC133—2基因的逆转录病毒表达载体。结果成功克隆AC133—2全长基因并构建PGEZ-Term-AC133-2逆转录病毒表达载体。结论AC133-2全长基因克隆及构建逆转录病毒表达载体的成功,为构建AC133-2转基因细胞和制备抗人AC133-2单克隆抗体和研究AC133-2的生物学功能奠定了物质基础。 Objective To clone AC133-2, construct retroviral vector. Methods AC 133-2 was cloned from fetal liver. The gene was ligated with T-Vectoe and sequenced to construct retroviral vector constisting of AC133-2. Results AC133-2 and construction of retroviral vector was cloned successfully. Conclusion Successful cloning of AC133-2 and construction of retroviral vector lays the foundation for constructed the AC 133-2 transgenic cells, and preparation and characterization of anti-AC133-2 McAbs.
出处 《苏州大学学报(医学版)》 CAS 北大核心 2005年第1期31-33,共3页 Suzhou University Journal of Medical Science
关键词 AC133—2基因 逆转录病毒表达载体 AC133-2 gene, retroviral vector
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参考文献7

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同被引文献7

  • 1王伟,汪洪毅,赵会霞,崔中光,李广伦.CD133抗原在白血病及MDS骨髓细胞中的表达[J].中国实验血液学杂志,2007,15(3):470-473. 被引量:4
  • 2Wu Y,Wu PY. CD133 as a marker for cancer stem cells: progresses and concerns[J]. Stem Cells Dev,2009,18(8) : 1127-1134.
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