Construction and Identification of Recombinant Adenoviral Plasmids Containing CXCL12 Gene
Zhu Zho
Abstract
Zhu Zho
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.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
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