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人MASP-2N端片段的原核表达
引用本文:刘洁,李伟,姜文静,贾天军,常晓彤. 人MASP-2N端片段的原核表达[J]. 国际免疫学杂志, 2011, 34(6): 381-383,396. DOI: 10.3760/cma.j.issn.1673-4394.2011.06.014
作者姓名:刘洁  李伟  姜文静  贾天军  常晓彤
作者单位:1. 河北北方学院医学检验学院,张家口,075000
2. 河北北方学院附属一院骨外科,张家口,075000
基金项目:河北省科技厅自然基金课题,张家口市科学技术与发展计划项目
摘    要:
目的 克隆并表达人MASP-2N端片段,为制备单克隆抗体及其临床应用奠定基础.方法 采用RT-PCR技术从人胎肝组织总RNA中扩增人MASP-2N端cDNA,克隆入pGEX-6p-2表达载体,在E.coli中表达GST- MASP-2N融合蛋白.结果 酶切图谱分析和DNA测序分析表明,成功构建了含人MASP-2N端片...

关 键 词:MASP-2N  RT-PCR  基因克隆  原核表达

Prokaryotic expression of the N-terminal Fragment of human mannose- binding lectin associated Serine Protein Kinase-2
LIU Jie,LI Wei,JIANG Wen-jing,JIA Tian-jun,CHANG Xiao-tong. Prokaryotic expression of the N-terminal Fragment of human mannose- binding lectin associated Serine Protein Kinase-2[J]. International Journal of Immunology, 2011, 34(6): 381-383,396. DOI: 10.3760/cma.j.issn.1673-4394.2011.06.014
Authors:LIU Jie  LI Wei  JIANG Wen-jing  JIA Tian-jun  CHANG Xiao-tong
Affiliation:.( College of Medicine Lab, HeBei North University, ZhangJiakou 075000, China)
Abstract:
Objective To clone and express the human MASP-2N-terminal fragment in E.coli.Methods Total RNA was extracted from human fetal liver tissue and MASP-2N cDNA was amplified by RT-PCR.The PCR product was cloned into pGEX-6p-2 vector.E.coli was transformed by the recombinant plasmid and GST- MASP-2N fusion protein was expressed.Results The constructed recombinant plasmids were identified by enzyme digestion and DNA sequencing.The recombinant protein was expressed in E.coli.Conclusion The N-terminal fragment of human MASP-2 was cloned and expressed.
Keywords:MASP-2N  RT-PCR  G ene cloning  Prokaryotic expression
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