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人血小板生成素(hTPO)全长 cDNA 克隆及在 CHO 细胞中的表达
引用本文:邢桂春, 郭树华, 胡志远, 张咏, 董波, 贺福初,. 人血小板生成素(hTPO)全长 cDNA 克隆及在 CHO 细胞中的表达[J]. 生物工程学报, 1997, 13(4)
作者姓名:邢桂春   郭树华   胡志远   张咏   董波   贺福初  
作者单位:北京放射医学研究所;
基金项目:863计划,自然科学基金
摘    要:以人胎肝mRNA为模板,采用RT-PCR扩增了人TPO编码区全长cDNA,全序列测定结果表明与国外报道序列一致;进而构建了pcDNA3-TPO永久表达载体,转染CHO细胞后经G418加压筛选、TPO表达稳定性等项指标测试,获得了稳定分泌TPO的工程细胞株。

关 键 词:人血小板生成素   PCR   序列分析   CFU-Meg   CHO细胞表达  

Cloning and Expression of a Full Length cDNA of Human Thrombopoietin (hTPO)in CHO Cells
Xing Guichun Guo Shuhua Hu Zhiyuan Zhang Yong Dong Bo He Fuchu. Cloning and Expression of a Full Length cDNA of Human Thrombopoietin (hTPO)in CHO Cells[J]. Chinese journal of biotechnology, 1997, 13(4)
Authors:Xing Guichun Guo Shuhua Hu Zhiyuan Zhang Yong Dong Bo He Fuchu
Abstract:A full length cDNA of the coding region of hTPO,whose sequence is identical to those previously reported,has been amplified by means of RT PCR with human fetal liver mRNA as the templates and then sequenced.Further,this insert was subcloned into a mammalian expression vector pcDNA3 (pcDNA3 TPO),transformed into CHO cells, and screened by G418 and then tested by expression level of hTPO.A group of stably secreting engineered strains of hTPO has been obtained.
Keywords:Human thrombopoietin  CFU Meg  CHO cell  PCR  sequencing analysis  expression
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