The yeast two-hybrid system is a novel and sensitive technique to detect protein-protein interactions in vivo.
酵母双杂合系统是在酵母细胞中研究蛋白- 蛋白相互作用的新技术。
Nevertheless, huge protein network is larger than that we predict and single yeast two-hybrid system cannot solve all the problems, which need be complemented by other wags.
但是巨大的蛋白质网络比我们想象要大得多，单一的双杂交系统不能解决所有问题，需要同其它的方法有效地结合。
RESULTS: human NS5ABP37 was screened and cloned from human liver cDNA library by yeast-two hybrid system 3. The murine NS5ABP37 was deduced by bioinformatics methods.
结果：通过酵母双杂交技术获得了人ns5abp37的编码基因。利用生物信息学技术确定了小鼠ns5abp37的基因序列。
Objective: To assay the transcriptional activation effect of prohibitin in yeast two hybrid system.
目的：检测抗增殖蛋白在酵母双杂交系统中是否具有转录自激活作用。
During the procedure, different molecular biology techniques were involved such as PCR RT-PCR and Yeast-two-hybrid system.
在试验过程中用到了很多高级的生物学技术，比如说PCR,RT - PCR和酵母双杂交技术。
The endocrine disrupting functions of 4 natural and synthetical estrogens, 4 phytoestrogens, 14 phenols widely used in the tap water supply system were detected using yeast two-hybrid technique.
利用酵母双杂交系统对4种天然和合成的雌激素，4种植物性激素以及14种常用于自来水供水系统中的酚类物质进行了内分泌干扰作用的筛检测定。
Conclusion Using yeast two-hybrid system, we got some alternative proteins which may interact with the cytoplasmic tail of NECL1.
结论应用酵母双杂交系统，获得了一些候选的NECL1胞内区相互作用蛋白。
In this paper, we use Yeast Two Hybrid System (Y2H) to screen the interacting protein of BKI1, and finally find AT2G06010.
我们使用酵母双杂交的方法，筛选到BKI1的一个互作蛋白，即AT2G06010基因编码的蛋白。
In this paper, we use Yeast Two Hybrid System (Y2H) to screen the interacting protein of BKI1, and finally find AT2G06010.
我们使用酵母双杂交的方法，筛选到BKI1的一个互作蛋白，即AT2G06010基因编码的蛋白。
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