Expression of porcine Toll-like receptor TLR2 gene in the CHO-K1 cells
Yongxi Dou
Abstract
Yongxi Dou
Abstract
The recombinant plasmid PcDNA3.1/CT-GFP-pTLR2 was transfected into the CHO-K1 cells by lipofectin and the positive cell clone was obtained after screening by G418 for 2~3 weeks.Analysis of the exogenous gene by PCR and RT-PCR indicated that the pTLR2 gene was integrated into the CHO-K1 cells.The expression of pTLR2-GFP fusion protein was observed by intensity fluorescence microscope at different time after transfection.The results indicated that pTLR2-GFP fusion protein was successfully expressed in the cells and these cells could be further used to investigate the functions of pTLR2.
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The recombinant plasmid PcDNA3.1/CT-GFP-pTLR2 was transfected into the CHO-K1 cells by lipofectin and the positive cell clone was obtained after screening by G418 for 2~3 weeks.Analysis of the exogenous gene by PCR and RT-PCR indicated that the pTLR2 gene was integrated into the CHO-K1 cells.The expression of pTLR2-GFP fusion protein was observed by intensity fluorescence microscope at different time after transfection.The results indicated that pTLR2-GFP fusion protein was successfully expressed in the cells and these cells could be further used to investigate the functions of pTLR2.
Key concepts: Transfection, Chinese hamster ovary cell, Molecular biology, Green fluorescent protein, Recombinant DNA, Fluorescence microscope, clone (Java method), Gene