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Construction and identification of human aquaporin 1 gene recombinant adenovirus

Yang Yan

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Abstract

Objective To construct the recombinant adenovirus of human aquaporin 1 (AQP1) gene. Methods The replication deficient recombinant adenovirus encoding hAQP 1(pAdEasy 1/ hAQP1) was constructed by the method of DNA recombination and homogenous recombination in bacteria. The ECV 304 cells were transfected by the recombinant adenovirus. The target gene was identified by polymerase chain reaction (PCR). The titer and the infection rate were determined using the green fluorescent protein (GFP) expression in the shuttle plasmid. Results Restriction endonuclease and PCR analyses confirmed that the recombinant adenovirus was successfully constructed. The infection rate was high. Conclusion The recombinant adenovirus pAdEasy 1/ hAQP1 has been successfully constructed by the method of homogenous recombination in bacteria.

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What this paper is about

Objective To construct the recombinant adenovirus of human aquaporin 1 (AQP1) gene. Methods The replication deficient recombinant adenovirus encoding hAQP 1(pAdEasy 1/ hAQP1) was constructed by the method of DNA recombination and homogenous recombination in bacteria. The ECV 304 cells were transfected by the recombinant adenovirus. The target gene was identified by polymerase chain reaction (PCR). The titer and the infection rate were determined using the green fluorescent protein (GFP) expression in the shuttle plasmid. Results Restriction endonuclease and PCR analyses confirmed that the recombinant adenovirus was successfully constructed. The infection rate was high. Conclusion The recombinant adenovirus pAdEasy 1/ hAQP1 has been successfully constructed by the method of homogenous recombination in bacteria.

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Available abstract

Objective To construct the recombinant adenovirus of human aquaporin 1 (AQP1) gene. Methods The replication deficient recombinant adenovirus encoding hAQP 1(pAdEasy 1/ hAQP1) was constructed by the method of DNA recombination and homogenous recombination in bacteria. The ECV 304 cells were transfected by the recombinant adenovirus. The target gene was identified by polymerase chain reaction (PCR). The titer and the infection rate were determined using the green fluorescent protein (GFP) expression in the shuttle plasmid. Results Restriction endonuclease and PCR analyses confirmed that the recombinant adenovirus was successfully constructed. The infection rate was high. Conclusion The recombinant adenovirus pAdEasy 1/ hAQP1 has been successfully constructed by the method of homogenous recombination in bacteria.

Key concepts: Recombinant DNA, Molecular biology, Homologous recombination, Biology, Plasmid, Virology, Gene, Restriction enzyme

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