2007Journal of Pathogen BiologyRequires access

Expression and identification of CsSCCRO gene of Clonorchis sinensis

YU Xin-bing

Open publisher page 0 citations

Abstract

Objective To transfect CsSCCRO gene to Hela cell,and detect transfection efficiency,so as to provide evidence for the encoding protein function research on the cellular level.Methods Cloned CsSCCRO gene to eukaryotic vector pEGFP-N1 and transfected the pEGFP-N1-CsSCCRO to Hela cell by the method of liposome,then identified the transfection efficiency by RT-PCR.Results Recombinant plasmid pEGFP-N1-CsSCCRO was successfully transfected to Hela cell,and fluorescin were expressed stably.A 780 bp length fragment was successfully cloned and identified by RT-PCR.Conclusion CsSCCRO gene can transfect to Hela cell and can be transcribed and translated to fusion protein with GFP efficiently.

About this research paper

What this paper is about

Objective To transfect CsSCCRO gene to Hela cell,and detect transfection efficiency,so as to provide evidence for the encoding protein function research on the cellular level.Methods Cloned CsSCCRO gene to eukaryotic vector pEGFP-N1 and transfected the pEGFP-N1-CsSCCRO to Hela cell by the method of liposome,then identified the transfection efficiency by RT-PCR.Results Recombinant plasmid pEGFP-N1-CsSCCRO was successfully transfected to Hela cell,and fluorescin were expressed stably.A 780 bp length fragment was successfully cloned and identified by RT-PCR.Conclusion CsSCCRO gene can transfect to Hela cell and can be transcribed and translated to fusion protein with GFP efficiently.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To transfect CsSCCRO gene to Hela cell,and detect transfection efficiency,so as to provide evidence for the encoding protein function research on the cellular level.Methods Cloned CsSCCRO gene to eukaryotic vector pEGFP-N1 and transfected the pEGFP-N1-CsSCCRO to Hela cell by the method of liposome,then identified the transfection efficiency by RT-PCR.Results Recombinant plasmid pEGFP-N1-CsSCCRO was successfully transfected to Hela cell,and fluorescin were expressed stably.A 780 bp length fragment was successfully cloned and identified by RT-PCR.Conclusion CsSCCRO gene can transfect to Hela cell and can be transcribed and translated to fusion protein with GFP efficiently.

Key concepts: Transfection, HeLa, Molecular biology, Biology, Recombinant DNA, Clonorchis sinensis, Gene, Fusion protein

Related papers

Back to paper searchBrowse research topicsOriginal source
Expression and identification of CsSCCRO gene of Clonorchis sinensis — Research Paper | ScholarLens