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人PLAGL2基因表达载体质4粒的构建
引用本文:邓飞涛,柴新群,吴超英,王泽华. 人PLAGL2基因表达载体质4粒的构建[J]. 中国优生与遗传杂志, 2008, 16(4): 11-12
作者姓名:邓飞涛  柴新群  吴超英  王泽华
作者单位:1. 华中科技大学同济医学院附属协和医院妇产科,武汉,430022
2. 华中科技大学同济医学院附属协和医院肝胆外科,武汉,430022
摘    要:
目的克隆人PLAGL2基因片段并插入(TetO)7-CMV表达载体。方法采用PCR技术扩增出人PLAGL2基因的两个DNA片段,经酶连后获得约2kb的目的DNA片段并插入(TetO)7-CMV载体中,PCR筛选阳性转化株并分析重组质粒的DNA序列。结果DNA测序结果显示重组质粒(TetO)7-CMV-PLAGL2序列正确。结论扩增并连接了人PLAGL2基因的两个DNA片段,最终成功构建了人PLAGL2基因的表达载体质粒-(TetO)7-CMV-PLAGL2。

关 键 词:PLAGL  2  (TetO)7-CMV  PCR  DNA序列分析
文章编号:1006-9534(2008)04-0011-03
修稿时间:2007-09-27

The construction of human PLAGL2 gene recombinant DNA plasmid
DENG Fei-tao,CHAI Xin-qun,WU Chao-ying,WANG Ze-hua. The construction of human PLAGL2 gene recombinant DNA plasmid[J]. Chinese Journal of Birth Health & Heredity, 2008, 16(4): 11-12
Authors:DENG Fei-tao  CHAI Xin-qun  WU Chao-ying  WANG Ze-hua
Affiliation:DENG Fei - tao, CHAI Xin - qun , WU Chno - ying, WANG Ze - hua ( 1. Department of Obstetric and Gynecology; 2. Department of Hepatobiliary Surgery, Union Hospital, Huazhong University of Science & Technology, Wuhan, 430022)
Abstract:
Objective: To clone DNA fragment of human PLAGL 2 gene and insert it into (TetO)7 - CMV expressive vector. Methods: The two DNA fragment of human PLAGL 2 gene was amplified from human genomic DNA respectively, then combined them with T4 DNA ligase, and then the 2kb combined DNA fragment was subcloned into (TetO)7 -CMV expressive vector. The plasmid was determined by DNA sequencing. Result: The results of DNA sequencing showed that the sequence of recombined DNA plasmid was correct. Conclusion: The DNA fragment of human PLAGL 2 gene was amplified and combined correctly, and recombined DNA plasmid of (TetO)7-CMV- PLAGL 2 was constructed successfully.
Keywords:PLAGL 2  (TetO)7 -CMV  PCR  DNA Sequence Analyzing
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