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人降钙素cDNA的化学合成与克隆
引用本文:蔡在龙 窦鸿. 人降钙素cDNA的化学合成与克隆[J]. 第二军医大学学报, 1996, 17(5): 447-449
作者姓名:蔡在龙 窦鸿
作者单位:第二军医大学基础医学部生物化学教研室
摘    要:目的;克隆人降钙素cDNA。方法和结果;应用ABI391DNA合成仪,将人降钙素cDNA分成6个片段合成。退火、磷酸化,连接,最终将人降钙素cDNA克隆于载体pGEM7Z(+),经DNA双链测离,证明克隆利的人降钙素cDNA序列与设计的完全一致。结论;本研究为寡肽cDNA的化学合成与克隆提供了简捷、可靠的方法;为人的降钙素DNA的主效表达奠定了基础。

关 键 词:降钙素 cDNA 化学合成 克隆

Chemical synthesis and cloning of human calcitonin cDNA
Cai Zailong, Dou Hong, Mao Jifang, Zou Lufeng, Wu Jun, Wang Guanjiang. Chemical synthesis and cloning of human calcitonin cDNA[J]. Former Academic Journal of Second Military Medical University, 1996, 17(5): 447-449
Authors:Cai Zailong   Dou Hong   Mao Jifang   Zou Lufeng   Wu Jun   Wang Guanjiang
Abstract:Objective: Chemical synthesis and cloning of human calcitonin (hCT) cDNA. Methods and Results: A cDNA coding for human calcitonin was divided into six fragments,synthesized by ABI 391 DNA synthesis instruments and cloned into pGEM7Z(+) vector following phosphorylation, annealing and ligation of six fragments and the sequence of cloned hCT cDNA was proved to be the same as designed. Conclusion: A reliable and forthright method of chemical synthesis of oligo-peptide cDNA (or gene)and cloning is provided in this study. This paper is a basic work for expression of hCT cDNA.
Keywords:human calcitonin  cDNA  chemical synthesis  clone
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