变复性实验是建立在对蛋白质体外折叠机制的了解的基础上。
The process of renaturation is established in the understanding to the mechanism of protein folding in vitro.
本章对色谱中的保留机理及理论、蛋白质液相色谱复性机理及蛋白折叠动力学理论模型研究进展进行了综述，共包括文献61篇。
In this chapter solute retention mechanism in LC, protein refolding mechanism and new developments in protein refolding kinetics were reviewed. It contains 61 references.
基因重组蛋白质的复性是当前生物工程领域的重要研究课题。
The renaturation of gene recombinant protein is the most important technique in the field of biotechnology which's many methods have been established.
目的探讨感光受体外周蛋白结合蛋白（PBP）在体外是否有促进变性蛋白质复性的作用。
Objective The possibility of peripherin binding protein (PBP) to improve the refolding of denatured luciferase in vitro was investigated.
探讨感光受体外周蛋白结合蛋白（PBP）在体外是否有促进变性蛋白质复性的作用。
The possibility of peripherin binding protein (PBP) to improve the refolding of denatured luciferase in vitro was investigated.
方法根据人工分子伴侣对重组蛋白质的复性机理，采用人工分子伴侣方法应用于重组内抑素的复性。
Methods Based on the reactive principle of molecular chaperone, we adopted an artificial molecular chaperone-assisted refolding method for recombinant endostatin refolding.
而利用分子伴侣的协助折叠特性进行的蛋白质复性技术正成为这一领域的研究热点。
Some kinds of molecular chaperone systems and their functions as well were reviewed in this paper.
同一批和不同批次重复分析的结果显示，方法的重复性和细菌特征性蛋白质谱图的重现性较好。
The repeated results of the same sample and different batches of culture have proved the reproducibility of the MALDI-TOF analysis.
目的：初步建立人晶状体蛋白质组研究中的双向电泳分离技术，提高晶状体蛋白分辨率和重复性。
Objective:To establish and optimize two-dimensional electrophoresis (2-DE) for proteonomic analysis of the human lens and to promote resolution and reproducibility.
目的：初步建立人晶状体蛋白质组研究中的双向电泳分离技术，提高晶状体蛋白分辨率和重复性。
Objective:To establish and optimize two-dimensional electrophoresis (2-DE) for proteonomic analysis of the human lens and to promote resolution and reproducibility.
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