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Transfection of insect cell lines using polyethylenimine.使用聚乙烯亚胺转染昆虫细胞系。
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Insect cell transformation vectors that support high level expression and promoter assessment in insect cell culture.支持昆虫细胞培养中高水平表达和启动子评估的昆虫细胞转化载体。
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本文引用的文献

1
Methods for maintaining insect cell cultures.维持昆虫细胞培养物的方法。
J Insect Sci. 2002;2:9. doi: 10.1093/jis/2.1.9. Epub 2002 May 20.
2
Systemic and in vitro infection process of Bombyx mori nucleopolyhedrovirus.家蚕核型多角体病毒的体内和体外感染过程
Virus Res. 2004 May;101(2):109-18. doi: 10.1016/j.virusres.2003.12.027.
3
Purification of DNA for the transfection of a Spodoptera frugiperda cell line.用于转染草地贪夜蛾细胞系的DNA纯化
Methods Cell Sci. 2002;24(4):155-63. doi: 10.1023/a:1024413604663.
4
Transfection of Lymantria dispar insect cell lines.舞毒蛾昆虫细胞系的转染
Methods Cell Sci. 2000;22(4):257-63. doi: 10.1023/a:1017533119177.
5
Production of selected baculoviruses in newly established lepidopteran cell lines.在新建立的鳞翅目昆虫细胞系中生产选定的杆状病毒。
In Vitro Cell Dev Biol Anim. 2001 Jun;37(6):374-9. doi: 10.1007/BF02577574.
6
A study of the Autographa californica multiple nucleopolyhedrovirus ODV envelope protein p74 using a GFP tag.利用绿色荧光蛋白标签对苜蓿银纹夜蛾多核多角体病毒(Autographa californica multiple nucleopolyhedrovirus)的病毒粒子囊膜蛋白p74进行的一项研究。
J Gen Virol. 2001 Sep;82(Pt 9):2279-2287. doi: 10.1099/0022-1317-82-9-2279.
7
Gene transfer with lipospermines and polyethylenimines.使用脂精胺和聚乙烯亚胺进行基因转移。
Adv Drug Deliv Rev. 1998 Mar 2;30(1-3):85-95. doi: 10.1016/s0169-409x(97)00109-9.
8
Systemic linear polyethylenimine (L-PEI)-mediated gene delivery in the mouse.小鼠体内系统性线性聚乙烯亚胺(L-PEI)介导的基因递送
J Gene Med. 2000 Mar-Apr;2(2):128-34. doi: 10.1002/(SICI)1521-2254(200003/04)2:2<128::AID-JGM95>3.0.CO;2-W.
9
Traditional and emerging methods for analyzing cell activity in cell culture.用于分析细胞培养中细胞活性的传统方法和新兴方法。
Methods Cell Sci. 2000 Mar;22(1):67-78. doi: 10.1023/a:1009839501174.
10
Use of flow cytometry to rapidly optimize the transfection of animal cells.使用流式细胞术快速优化动物细胞转染
Biotechniques. 2000 Jan;28(1):148-54. doi: 10.2144/00281rr03.

使用聚乙烯亚胺转染昆虫细胞系。

Transfection of insect cell lines using polyethylenimine.

机构信息

Institute of Genetics and Plant Experimental Biology, Uzbek Academy of Science Tashkent region, Qibray district, Yuqori-Yuz, 702151, Uzbekistan.

出版信息

Cytotechnology. 2006 Jun;51(2):89-98. doi: 10.1007/s10616-006-9022-7. Epub 2006 Nov 2.

DOI:10.1007/s10616-006-9022-7
PMID:19002899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3449679/
Abstract

Insect cell lines have been widely used in recombinant baculovirus expression systems and transient gene expression studies. Critical to these applications have been the transfection of foreign DNA. This has been frequently done using labor intensive and cytotoxic liposome-based transfection reagents. In the current study we have optimized a new kind of polyethylenimine-based DNA transfection reagent on the Spodoptera frugiperda Sf9 insect cell line. A plasmid vector that transiently expresses green fluorescent protein (GFP) was effectively delivered into Sf9 cells. A transfection efficiency of 54% and cell viability of 85-90% were obtained for Sf9 cells. The developed transfection protocol has now been successfully used to transfect eight insect cell lines derived from Bombyx mori, Trichoplusia ni, Helicoverpa zea, Heliothis virescens and S. frugiperda with GFP and GUS with transfection efficiencies of at least 45%. This method provides high heterologous protein expression levels, transfection efficacy and cell viability, and could be used for transient gene expression in other lepidopteran cell lines.

摘要

昆虫细胞系已广泛应用于重组杆状病毒表达系统和瞬时基因表达研究。这些应用的关键是外源 DNA 的转染。这通常是通过使用劳动密集型和细胞毒性的脂质体转染试剂来完成的。在本研究中,我们对 Spodoptera frugiperda Sf9 昆虫细胞系上的一种新型聚乙烯亚胺基 DNA 转染试剂进行了优化。一个瞬时表达绿色荧光蛋白 (GFP) 的质粒载体被有效地递送到 Sf9 细胞中。Sf9 细胞的转染效率为 54%,细胞活力为 85-90%。该转染方案现已成功用于转染来自家蚕、棉铃虫、玉米螟、烟青虫和 S. frugiperda 的八种昆虫细胞系,转染 GFP 和 GUS 的效率至少为 45%。该方法提供了高的异源蛋白表达水平、转染效率和细胞活力,可用于其他鳞翅目细胞系的瞬时基因表达。