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- 結論成功地構建了人sTNFR1重組質粒克隆,表達並純化了sTNFR1-MBP融合蛋白。sTNFR1-MBP was produced in E. Coli after IPTG induction, and a 66 KD sTNFR1-MBP was purified by ARAC. [WTHZ]Conclusion Recombinant plasmid carrying human sTNFR1 cDNA was successfully constructed and epxressed in E.
- 人sTNFR1human sTNFR1
- 結果經核苷酸序列測序和SDS-PAGE法鑒定,成功構建了人sTNFR1重組質粒基因工程菌,並表達和純化了sTNFR-MBP融合蛋白。Coli JM109, and induced by IPTG to express fusion protein sTNFR1-MBP. sTNFR1-MBP was purified by amylose resin affinity chromatography(ARAC), and analyzed by SDS-PAGE. Results A 558 bp human sTNFR1 cDNA was amplified by RT-PCR, and successfully inserted into plasmid pMAL-c2x.
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