2002Acta Universitatis Medicinalis Secondae ShanghaiRequires access

The Construction of Dominant Negative Mutant Plasmid pCDNA4 - C - GFPand Its in vitro Expression

Bin Wang

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Abstract

To investigate the construction of pCDNA4 - C - GFP and its in vitro expression. Methods The DNA plasmid pCDNA4 - C- GFP, which contains the C gene encoding core protein of HBV and green fluorescent protein gene, was constructed by gene technology. The plasmid pCDNA4 - C - GFP was transferred into the cell line HepG2. The in vitro expression of the plasmid was observed. Results Transcripts of the plasmid were detected by RT- PCR, and the GFP expession was detected by confocal. Conclusion The plasmid pCDNA4 - C- GFP can be used for its functional research.

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What this paper is about

To investigate the construction of pCDNA4 - C - GFP and its in vitro expression. Methods The DNA plasmid pCDNA4 - C- GFP, which contains the C gene encoding core protein of HBV and green fluorescent protein gene, was constructed by gene technology. The plasmid pCDNA4 - C - GFP was transferred into the cell line HepG2. The in vitro expression of the plasmid was observed. Results Transcripts of the plasmid were detected by RT- PCR, and the GFP expession was detected by confocal. Conclusion The plasmid pCDNA4 - C- GFP can be used for its functional research.

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Available abstract

To investigate the construction of pCDNA4 - C - GFP and its in vitro expression. Methods The DNA plasmid pCDNA4 - C- GFP, which contains the C gene encoding core protein of HBV and green fluorescent protein gene, was constructed by gene technology. The plasmid pCDNA4 - C - GFP was transferred into the cell line HepG2. The in vitro expression of the plasmid was observed. Results Transcripts of the plasmid were detected by RT- PCR, and the GFP expession was detected by confocal. Conclusion The plasmid pCDNA4 - C- GFP can be used for its functional research.

Key concepts: Plasmid, Green fluorescent protein, Molecular biology, Gene, In vitro, Mutant, Biology, Gene expression

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