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论著

Fn14-shRNA慢病毒载体的制备

  • 于涛 杨云峰 李兵 陈凯 朱辉 张明珠 赵有光 俞光荣
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  • 1. 上海市同济医院,同济大学附属同济医院
    2. 上海市同济医院同康楼

收稿日期: 2016-01-18

  修回日期: 2016-01-19

  网络出版日期: 2016-09-13

Construction and identification of Fn14-shRNA lentiviral vector

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Received date: 2016-01-18

  Revised date: 2016-01-19

  Online published: 2016-09-13

摘要

目的 构建Fn14-shRNA慢病毒载体,以进一步进行动物实验,研究Fn14在骨肉瘤中的表达和作用。方法 使用RNA干扰技术,构建Fn14干扰载体、病毒包装、感染细胞,并进行鉴定。结果 Fn14-shRNA干扰质粒单酶切验证阳性,测序结果与设计完全一致,干扰组Fn14在稳转细胞株中表达下调。 结论 成功构建了Fn14-shRNA慢病毒载体,为进一步从分子水平探讨Fn14在骨肉瘤中的生物学作用奠定了基础。

本文引用格式

于涛 杨云峰 李兵 陈凯 朱辉 张明珠 赵有光 俞光荣 . Fn14-shRNA慢病毒载体的制备[J]. 外科研究与新技术(中英文), 2016 , 5(2) : 96 -101 . DOI: 10.3969/j.issn.2095-378X.2016.02.008

Abstract

Objective To construct a Fn14-shRNA lentiviral vector to further study the expression and biological significance of Fn14 in osteosarcoma with animal experiment. Methods Constructing Fn14-shRNA vector by RNA interference technique, viral packaging, co-transfecting cells and indentification. Results Single enzyme detection was positive, sequencing result was consistent with design, Fn14 was downregulated in stably transfected cell lines. Conclusion The Fn14-sh RNA lentivirus recombinant vectors were successfully constructed which laid the foundation for further study of the biological significance of Fn14 in osteosarcoma.

参考文献

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