Cloning expression and purification of recombinant thymosin #alpha#_(1)
Zhaolong Gong, Zuo-jun Jiang, Yihui Xu, Jilong Shen, Wei Dong, Zhaojun Duan
Abstract
Zhaolong Gong, Zuo-jun Jiang, Yihui Xu, Jilong Shen, Wei Dong, Zhaojun Duan
Abstract
The fusion gene composed of Ref (a sort of T7 phage protein) and T#alpha#_(1) gene was synthesized, and the gene was cloned into expression vector pBV220, E.coliDH5#alpha# was transformed with recombinant plasmid and induced by temperature. The expressed fusion protein could be purified by CM-Sepharose Fast Flow cation exchange chromatography and identified by Western-blot. The purified fusion protein, Ref-T#alpha#_(1) was obtained. The molecular weight was about 15000. To express short peptide, the method of expressing fusion gene is practical. The successful expression of Ref-T#alpha#_(1) has established a foundation for biological activity research.
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The fusion gene composed of Ref (a sort of T7 phage protein) and T#alpha#_(1) gene was synthesized, and the gene was cloned into expression vector pBV220, E.coliDH5#alpha# was transformed with recombinant plasmid and induced by temperature. The expressed fusion protein could be purified by CM-Sepharose Fast Flow cation exchange chromatography and identified by Western-blot. The purified fusion protein, Ref-T#alpha#_(1) was obtained. The molecular weight was about 15000. To express short peptide, the method of expressing fusion gene is practical. The successful expression of Ref-T#alpha#_(1) has established a foundation for biological activity research.
Key concepts: Recombinant DNA, Fusion protein, Molecular biology, Cloning (programming), Fusion gene, Molecular cloning, Alpha (finance), Expression vector