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Construction and expression of human anti-HAV Fab eukaryotic expression vector

Changming Yu, Jing Xu, Guoqi Liu, Yigang Tong, Hongbin Song, Zhikai Xu, Haitao Wang

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Abstract

Fd and light chain genes were ligated to their signal peptide sequences and inserted into pCdhfr1 or pCDNA3.1, respectively. The recombinant plasmids were co-transfected into CHO cells, and resistant clones were obtained by G418 selection. The expression of Fab gene was detected by ELISA. Recombinant plasmids were successfully constructed. The plasmid-transfected CHO cells were obtained by co-transfection and G418 selection. ELISA confirmed the expression of anti-HAV Fab in culture medium.

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What this paper is about

Fd and light chain genes were ligated to their signal peptide sequences and inserted into pCdhfr1 or pCDNA3.1, respectively. The recombinant plasmids were co-transfected into CHO cells, and resistant clones were obtained by G418 selection. The expression of Fab gene was detected by ELISA. Recombinant plasmids were successfully constructed. The plasmid-transfected CHO cells were obtained by co-transfection and G418 selection. ELISA confirmed the expression of anti-HAV Fab in culture medium.

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Available abstract

Fd and light chain genes were ligated to their signal peptide sequences and inserted into pCdhfr1 or pCDNA3.1, respectively. The recombinant plasmids were co-transfected into CHO cells, and resistant clones were obtained by G418 selection. The expression of Fab gene was detected by ELISA. Recombinant plasmids were successfully constructed. The plasmid-transfected CHO cells were obtained by co-transfection and G418 selection. ELISA confirmed the expression of anti-HAV Fab in culture medium.

Key concepts: Plasmid, Recombinant DNA, Transfection, Molecular biology, Gene, Biology, Expression vector, Vector (molecular biology)

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