... 原核细胞型 Prokaryote 原核细胞表达 procaryotic expression ; prokaryotic expression 原核细胞基因 prokaryotic gene ...
基于1个网页-相关网页
The object of this study is hALR, focus on its molecular cloning, construction of eucaryote expression vector and procaryotic expression.
本课题选用hALR作为研究对象，重点研究其分子克隆、真核表达载体构建及原核表达。
参考来源 - 人肝再生增强因子基因的克隆、真核表达载体构建及原核表达We integrated GOBP2 gene into procaryotic expression vector. The recombinant protein is integrated with HisTag that is a purification of this protein which establish foundation to research the structure and the affinity of ligand.
本研究将烟夜蛾普通气味结合蛋白2基因整合入原核表达载体表达，得到的重组蛋白在其N-端融合有His·Tag纯化标记，为下一步获得大量GOBPZ重组蛋白，研究GOBPZ蛋白的结构及配体的研究奠定了基础。
参考来源 - 烟夜蛾触角普通气味结合蛋白2cDNA的克隆、序列分析及在大肠杆菌中的表达·2,447,543篇论文数据，部分数据来源于NoteExpress
The protein of procaryotic expression exists both in the supernatant fluid and the sediment.
原核表达的蛋白质无论在沉淀中还是在上清中均有表达。
Objective: to obtain the procaryotic expression vector containing the antifreeze protein gene AFP.
目的构建可用于大肠杆菌表达系统的含抗冻蛋白基因afp的表达载体。
Conclusion The more effective CHM-I clone with high purity could be expressed by procaryotic expression system.
结论原核表达系统可有效克隆较高纯度的CHM - I基因。
应用推荐