It's very useful for the cloning and expression of the autonomously repli-acting sequence from the eukaryotic DNA such as rice DNA.
该质粒可用于筛选水稻等真核生物DNA中的自主复制序列。
The cloning and expression analysis of BmCcnl1 provide the basis for the research of the embryonic development and cell cycle regulation.
对该基因的克隆和表达分析为今后研究家蚕胚胎发育及细胞周期调控奠定了基础。
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.
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。
This thesis focus on the cloning, expression, purification and structural and functional studies of domains of human disease related proteins.
本论文工作的重点是与人类疾病相关的蛋白质的结构域的克隆表达及结构、功能的研究。
The cloning, expression and controlling of specific genes in developing pollen were reviewed briefly.
对花粉发育及其特异基因的克隆、表达和调控进行了综述。
Along with the development of bioinformatics and genetic localization, EST has already become a powerful tool for mapping, cloning and expression profiling of genes.
随着生物信息学和基因定位的迅猛发展，EST已成为基因定位、基因克隆、基因表达分析的有力工具。
The gene structure of antibacterial peptides and the research of cloning and expression of the genes are .
本文主要综述了抗菌肽基因的克隆与表达的研究进展并展望了抗菌肽在畜牧业生产中的应用前景。
This review introduced the structure and function of melatonin receptor 1b, the cloning and structure, developmental expression, mapping and polymorphism of melatonin receptor 1b gene.
作者介绍了褪黑激素受体1b的结构和功能，褪黑激素受体1b基因的克隆及基因结构、发育性表达与作用、定位与多态性，并讨论了该基因与繁殖季节性的关系。
We established the techniques of screening the plasmid expression library and cloning the immunogen genes.
建立了筛选质粒表达文库和克隆免疫原基因的技术方法。
Objective:To analyze the N-terminal amino acid sequence of bovine cementum attachment protein(CAP), which lay a theoretical foundation for cloning and expression of the CAP.
目的：对牛牙骨质附着蛋白进行N末端氨基酸序列分析，为牙骨质附着蛋白的克隆表达提供一定的理论依据。
This paper is an introduction of the higher plant NADP-ME in the aspect of cloning, function and regulation of gene expression.
文章就高等植物NADP - ME的克隆、功能和基因表达调控方面作一介绍。
We isolated and purified EBP effectively, and obtained EBP with biological activity for the first time with gene cloning method and prokaryotic expression system.
通过基因克隆等方法，选择原核表达系统，并对目的蛋白进行分离纯化，初步获得有活性的人内毒素结合肽ebp。
Conclusions the success of cloning and expression of SEA in E. coli provides basis for study the preparation of monoclonal antibody and diagnostic reagent.
结论SEA基因成功克隆到表达质粒内并表达，为制备单抗、诊断试剂及其致病机制研究奠定了基础。
Result shows that cloning purpose fragment has the function of promoter, and it can regulate lower reaches gene expression intensely in drought, high-salt and cold.
结果表明克隆到的目的片段具有启动子功能，并且在干旱、高盐、低温诱导胁迫下更能强烈地驱动下游基因的表达。
Here we reported the cloning of the gene from murine tyrosinase, the expression of wild tyrosinase and variants in E. coli.
本文报道了在克隆了小鼠酪氨酸酶基因的基础上，在大肠杆菌表达体系中诱导表达野生型和变异型酪氨酸酶的结果。
Purpose: AQP4 M23 gene cloning and construction in the expression vector can provide us a research tool.
目的克隆大鼠水通道蛋白4（AQP4）M23基因并构建其载体为进一步研究提供理论基础和研究工具。
Purpose: AQP4 M23 gene cloning and construction in the expression vector can provide us a research tool.
目的克隆大鼠水通道蛋白4（AQP4）M23基因并构建其载体为进一步研究提供理论基础和研究工具。
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