Abstract

Objective: To synthesize the gene of human dominant-negative transforming growth factor beta receptor (DNTβRⅡ) by means of oligo chemic synthesis and PCR amplification, construct pTAR-GET-DNTβRⅡ eukaryotic expression vector and investigate whether its expression in breast cancer COS-7 cells. Methods: The DNTβRⅡ gene fragment were inserted into pTAR-GET to conduct a eukaryotic plasmid, then sequenced and identified by restrictive endonuclease digestion. Construction of eukaryotic expression vector pTAR-GET-DNTβRⅡ and transfected it into COS-7 cells, evaluate its expression by RT-PCR method. Results: The construction of eukaryotic expression vector pTAR-GET-DNTβRⅡand transfected it into COS-7 cells, DNTβRⅡ was instantaneously transfected and expressed in COS-7 cells successfully. Conclusion: Full length gene of DNTβRⅡ can be synthesized by means of oligo chemic synthesis and PCR amplification. The construction of eukaryotic expression vector pTAR-GET-DNTβRⅡ and express it successfully in breast cancer COS-7 cells, may provide basis for further study of breast cancer anti-tumor immunotherapy by adoptive immune cell therapy.

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