人IL-2基因腺病毒载体的构建和包装。
该表达载体的构建为获得大量NS1蛋白进行功能研究及抗体制备提供了基础。
Construction of the prokaryotic expression vector provided a foundation for further studying the function of NS1 protein and preparation of NS1 antibody.
完成了NKG2D的原核表达载体的构建，表达并纯化了重组NKG2D蛋白。
The NKG2D prokaryotic expression vector was successfully constructed. The recombinant NKG2D is expressed and purified.
HBV靶向核糖核酸酶真核表达载体的构建及其在2.2.15细胞内的表达。
Construction of HBV targeted ribonuclease and its expression in 2.2.15 cell line.
该表达载体的构建为进一步研究人id4基因的启动子活性及表达调控奠定了基础。
The construction of expression vector of human ID4 promoter provides a platform for further researches on promoter activity and expression regulation of human ID4 gene.
人血管生成素-1基因的克隆及表达载体的构建，为进一步研究其功能、活性和应用奠定了基础。
The cloning of human angiopoietin 1 gene and construction of it's expression vectors lay a good foundation of further study on the function, biological activity and application.
该启动子的成功克隆和其报告基因载体的构建，为研究SOD2的基因表达调控机制提供了重要基础和工具。
The reporter gene vector driven by SOD2 promoter will provide an experimental tool for the further study on the regulatory mechanism of the SOD2 expression.
结论：原核表达载体的构建、重组蛋白的表达、纯化及多克隆抗体的制备为今后研究该蛋白的功能提供了良好的基础。
CONCLUSION: Recombined prokaryotic expression vector, the purified protein and prepared polyclonal antibody were the necessary materials for further study of this protein.
在腺病毒载体的构建过程中，早期和晚期启动子的选择、构建以及去除末端蛋白(TP)、克隆末端序列是至关重要的。
The selection and cloning of early and late promoters and removal of adenovirus terminal protein (TP) are very important in construction of adenovirus vector.
结论野生型和突变型PRPF31基因真核表达载体的构建，为研究PRPF31基因突变引起视网膜色素变性的机制奠定了基础。
Conclusion Construction of the eukaryotic expression vectors of wild type and mutant PRPF31 genes is basic work for research on the mechanisms of retinitis pigmentosa caused by PRPF31 mutation.
重点讨论了各种检测方法在实际中的应用，百合无症病毒提取过程中需要解决的问题，外壳蛋白基因在大肠杆菌中表达载体的构建。
The discussion was mainly focused on the application of these detection methods, the problem result in the virus extraction progress, and the construction of expression plasmid having LSV CP gene.
本研究旨在构建具有猪 MSTN 前肽基因定点突变的真核表达载体。
This research intended to construct a eukaryotic expression vector with a site-directed mutation of porcine MSTN propeptide gene.
构建了鹦鹉热衣原体主要外膜蛋白的表达载体。
An expressing vector of major outer-membrane protein of Chlamydia psittaci was constructed.
文章报道了一种简便、通用、高效的复杂载体构建方法。
In this paper, a simple universal high-throughput method of constructing the vectors was developed.
目的构建狂犬病病毒糖蛋白基因的真核细胞表达载体，并在COS - 7细胞中表达。
Objective To construct a recombinant plasmid for expression of rabies virus glycoprotein in COS-7 cells.
文章综述了近年来牛腺病毒载体构建的一些研究进展。
The paper reviewed progress on the construction of bovine adenovirus vectors.
目的构建木瓜凝乳蛋白酶的表达载体，并在大肠杆菌中表达。
Objective To construct recombinant plasmid for expression of chymopapain in E.
为构建其启动外源基因的质粒表达载体作准备。
It was therefore preparation for constructing an expression plasmid vector to express exogenous genes.
目的：构建缺氧诱导表达载体，以介导报告基因在缺氧环境下的特异、高效表达。
Objective: to construct hypoxia-inducible expression vector, which mediated reporter gene to express specially and efficiently in hypoxia environment.
实验结果表明，以TK基因构建的重组载体质粒可用于外源基因的重组表达研究。
The result showed that the transfer vector plasmid constructed with FPVTK genes can be used to express foreign gene in FPV recombinant.
目的构建人il -12的高效表达载体。
Objetive to construct human IL 12 efficient expression vector.
目的：构建高免疫原性的抑制素真核表达载体。
Objective: to construct inhibin expression vector with high immunogenicity.
结论已成功地构建了人胰岛素基因的植物细胞表达载体。
Conclusion The vector for expression of human insulin in plant cells was successfully constructed.
结论胶原凝胶复合bcm支架可作为软骨细胞的载体体外构建组织工程软骨。
Conclusion Combination collagen gel with BCM can be used as a vehicle for chondrocytes to construct tissue-engineered cartilage in vitro.
化学基本观念是化学知识的提炼与升华，化学知识是构建化学基本观念的工具与载体。
Chemical basic concept is the refining and chemical knowledge distillation, chemical knowledge is a basic chemical building tools and the concept of vector.
在对港口与城市互动关系的分析的基础上，本文构建了以港口为核心、以城市为载体、以临港工业为依托的港口经济系统。
Based on analysis of the interaction relationship between the port and city, this article constructs the port economy system with the port being the core.
将胰岛素原基因融合到金色葡萄球菌蛋白a的基因上，构建成大肠杆菌中基因融合的外分泌表达载体。
The secretion expression vector of fusion gene in E. coli has constructed by fussing the proinsulin gene to the gene of staphylococcal protein a.
将胰岛素原基因融合到金色葡萄球菌蛋白a的基因上，构建成大肠杆菌中基因融合的外分泌表达载体。
The secretion expression vector of fusion gene in E. coli has constructed by fussing the proinsulin gene to the gene of staphylococcal protein a.
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