PDF(964 KB)
Construction and identification of eukaryotic expression vector of mouse SGK1 gene
Lina ZHANG, Long BA, Jun MENG
PDF(964 KB)
PDF(964 KB)
Construction and identification of eukaryotic expression vector of mouse SGK1 gene
Objective To construct an eukaryotic expression vector pcDNA3.1-MYC-SGK1-mcherry which containing mouse serum and glucocorticoid-induced kinase (SGK)1 gene, and to observe its expression in the transfected HEK293 cells. Methods The SGK1 target gene segments were amplified by PCR method, and the segments were ligated to the pcDNA3.1-MYC-C-mcherry vector which was doubly-digested with Hind Ⅲ and Sbf Ⅰ. After successful verification by enzyme digestion and sequencing, the pcDNA3.1-MYC-SGK1-mcherry expression vector was transfected into the HEK293 cells by liposome transfection. Western blotting method was used to determine the expression level of eukaryotic expression vector in the cells. Results The vector band was located at 5 200 bp and the target gene band was located at 3 100 bp, which was consistent with the expected results. The sequencing results were also consistent when compared with the expected sequence by Snap Gene software, which indicated that the eukaryotic expression vector pcDNA3.1-MYC-SGK1-mcherry was successfully constructed. Successful expression of the eukaryotic expression vector pcDNA3.1-MYC-SGK1-mcherry was observed by Western blotting method, in which the transfected cells showed well-defined bands near the relative molecular mass of 49 000. Conclusion The eukaryotic expression vector pcDNA3.1-MYC-SGK1-mcherry is successfully constructed, laying a solid foundation for the subsequent study on the transition mechanism of SGK1 gene in the early development of mouse fertilized egg cells.
Serum and glucocorticoid-induced kinase 1 / Eukaryotic expression vector / HEK293 cells / Vector construction / Plasmids
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张慧灵, 韩 迪, 郭文秀, 等. SGK1对Cyclin B/Cdc2通路介导小鼠G1期受精卵卵裂的调控作用及其机制[J].吉林大学学报(医学版), 2024, 50(3): 628-637.
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张丽娜参与实验研究、数据采集和论文撰写,巴隆参与实验研究、文献整理和论文修改,孟峻参与论文修改和审校。
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