摘要
目的 :构建高效表达人透明带蛋白 3的真核重组表达载体。方法 :利用 PCR、T- A载体克隆和亚克隆等技术。结果 :构建成 p GEM- ZP3重组质粒及 pc DNA3.1ZP3dhfr真核重组表达载体。结论 :经酶切鉴定构建的人透明带蛋白 3重组表达载体可高效表达重组人 ZP3蛋白。
Objective To construct the recombinant plasmid that highly expressed human zona pellucida 3. Methods The techniques of PCR amplification, T-A vector ligation, and sub-clone were used. Results The pGEM-TZP3 plasmid and pcDNA3.1ZP3dhfr recombinant expression vector were successfully constructed. Conclusion The recombinant expression plasmid constructed by restriction enzyme cleave identification can highly express recombinant human ZP3 protein.
出处
《吉林大学学报(医学版)》
CAS
CSCD
北大核心
2004年第5期681-683,共3页
Journal of Jilin University:Medicine Edition
基金
国家自然科学基金资助课题 (39870 313)
关键词
基因重组
透明带蛋白3
质粒
gene recombination
zona pellucida 3
plasmid