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- W2938283322 abstract "Apoptin is intensively studied for its potential as a therapeutic protein for cancer treatment since it is capable of inducing apoptosis specifically in cancer cells. Production of apoptin gene on a larger scale is important for the further application, and currently being studied by researchers around the world. In this research, chicken anemia virus apoptin optimized genetically for expression in Escherichia coli and modified using (His)6 tag, (Arg)8 tag, and HlyA tag intended for purification needs, penetration enhancement, and secretion from bacterial host to the growth media. Removal of (His)6 tag and HlyA tag were designed using a specific thrombin proteolytic site, while (Arg)8 tag was preserved. The gene designed, optimized and constructed in vector pET9a, then analyzed using Agarose Electrophoresis and Sequencing. The DNA sequencing result shows that the designed gene has successfully constructed." @default.
- W2938283322 created "2019-04-25" @default.
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- W2938283322 date "2019-01-01" @default.
- W2938283322 modified "2023-09-26" @default.
- W2938283322 title "Apoptin gene optimization in Escherichia coli" @default.
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- W2938283322 doi "https://doi.org/10.1063/1.5096733" @default.
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