2010•Neural Injury and Functional ReconstructionRequires access

Construction and Identification of Recombinant Adenoviral Plasmids Containing CXCL12 Gene

Zhu Zho

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Abstract

Objective: To construct and identify the recombinant adenoviral plasmids containing exogenous CXCL12 gene and EGFP gene and to investigate the expression of target genes.Methods: Genetic engineering techniques were used to construct the recombinant plasmids of pShuttle2-CXCL12-EGFP.The adenoviral plasmids pAdeno-CXCL12-EGFP were constructed by Adeno-X expression system.The plasmids were identified.Recombinant adenoviral vectors were packaged by cell line 293.The expression of EGFP was detected under the fluorescence microscopy.Results: The pShuttle2-CXCL12-EGFP was successfully constructed and identified by enzymolysis and sequencing.The adenoviral plasmids pAdeno-CXCL12-EGFP were successfully constructed and identified by enzymolysis and PCR.The expression of EGFP could be observed after the plasmids pAdeno-CXCL12-EGFP were transfected.Conclusion: The adenoviral plasmids containing CXCL12 gene and EGFP gene were constructed successfully by Adeno-X system.

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What this paper is about

Objective: To construct and identify the recombinant adenoviral plasmids containing exogenous CXCL12 gene and EGFP gene and to investigate the expression of target genes.Methods: Genetic engineering techniques were used to construct the recombinant plasmids of pShuttle2-CXCL12-EGFP.The adenoviral plasmids pAdeno-CXCL12-EGFP were constructed by Adeno-X expression system.The plasmids were identified.Recombinant adenoviral vectors were packaged by cell line 293.The expression of EGFP was detected under the fluorescence microscopy.Results: The pShuttle2-CXCL12-EGFP was successfully constructed and identified by enzymolysis and sequencing.The adenoviral plasmids pAdeno-CXCL12-EGFP were successfully constructed and identified by enzymolysis and PCR.The expression of EGFP could be observed after the plasmids pAdeno-CXCL12-EGFP were transfected.Conclusion: The adenoviral plasmids containing CXCL12 gene and EGFP gene were constructed successfully by Adeno-X system.

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Available abstract

Objective: To construct and identify the recombinant adenoviral plasmids containing exogenous CXCL12 gene and EGFP gene and to investigate the expression of target genes.Methods: Genetic engineering techniques were used to construct the recombinant plasmids of pShuttle2-CXCL12-EGFP.The adenoviral plasmids pAdeno-CXCL12-EGFP were constructed by Adeno-X expression system.The plasmids were identified.Recombinant adenoviral vectors were packaged by cell line 293.The expression of EGFP was detected under the fluorescence microscopy.Results: The pShuttle2-CXCL12-EGFP was successfully constructed and identified by enzymolysis and sequencing.The adenoviral plasmids pAdeno-CXCL12-EGFP were successfully constructed and identified by enzymolysis and PCR.The expression of EGFP could be observed after the plasmids pAdeno-CXCL12-EGFP were transfected.Conclusion: The adenoviral plasmids containing CXCL12 gene and EGFP gene were constructed successfully by Adeno-X system.

Key concepts: Plasmid, Recombinant DNA, Green fluorescent protein, Biology, Molecular biology, Gene, Transfection, Gene expression

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