Abstract
Objective: To construct a eukaryotic expression plasmidpcDNA3.1(−)-Humanin. Methods: The recombinant plasmid pGEMEX-1-Humanin was digested with restriction endonucleases BamH I and Hind III and the Humanin gene fragments, about 100 bp length, were obtained. Then the Humanin gene fragments were inserted into eukaryotic expression vector pcDNA3.1(−) and the recombinant plasmids pcDNA3.1(−)-Humanin were identified by sequencing. Results: Recombinant plasmid DNA successfully produced a band which had the same size as that of the Humanin positive control. The sequence of recombinant plasmids accorded with the Humnain gene sequence. Conclusions: A eukaryotic expression plasmid of Humanin was successfully constructed.
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Project (No. 2003C30040) supported by the Science and Technology Department of Zhejiang Province, China
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Luo, By., Chen, Xm., Tang, M. et al. Construction of a eukaryotic expression plasmid of Humanin. J Zheijang Univ Sci B 6, 11–13 (2005). https://doi.org/10.1631/jzus.2005.B0011
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DOI: https://doi.org/10.1631/jzus.2005.B0011