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作 者:吴晓燕[1] 雒文田[1] 徐利[1] 田竹芳[1] 王琛[1] 施秉银[1] 朱本章[1]
出 处:《中华内分泌代谢杂志》2004年第5期470-471,共2页Chinese Journal of Endocrinology and Metabolism
基 金:卫生部直属单位临床学科重点资助项目〔2 2 (0 55)〕
摘 要:利用基因重组方法 ,构建hTSHRecd基因片段原核表达系统 (E .coliM15 )。hTSHRecd蛋白表达量大 ,纯化得到毫克级高纯度的hTSHRecd蛋白 ,可与TSHR自身抗体及TSH特异性结合 。By gene recombination, the coding fragment of hTSHRecd was generated, and transformed into E.coli M15. hTSHRecd was high efficiently expressed in E.coli M15. After purification, milligrams of pure hTSHRecd was obtained, which was well recognized by hTSHR autoantibodies and TSH. Large quantities of well-characterized hTSHecd with immunological and some biological activity were produced.
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