Until recently , it has been quite difficult to analyze each reaction on a real - time basis using currently available biochemical or biophysical methods 目前运用传统的生物化学和生物物理的方法难以真正实现对生物分子相互作用的实时分析。
The displacement chromatography and its experimental conditions are introduced . state - of - the - art in separation and purification of biomolecules is reviewed 摘要介绍了置换色谱及其实验条件，总结了该技术在生物分子分离纯化方面的研究进展。
Ms method had a potenial to develop a novel diagnse method for drior cell . lh mpter 3 , the dctection of plam virus was developed by the use of mb 第五章，研究了溶胶凝胶法固定生物分子的新方法，使用了一种新的制备和保存g方法使得溶胶
The primary subject of biosensing studies is the immobilization of biomolecules at sensing interface and the signaling of specific events of biological interaction 生物传感器研究的核心内容是传感界面生物分子的固定化技术及生物识别的信号转换技术。
Thus , it becomes an importam issue to observe , measul ' e and analyze the biological reactions within the living organism as transient and dynamic reaction 由于细胞内分子间的相互作用是一个动态平衡过程，因此实时分析生物分子间短暂的动态过程是必要的。
The method was carried out by in situ synthesizing a conducting polymer in a porous polymer film and co - immobilizing biomolecule in the composite film 该方法的原理是：在一种多孔高分子膜中原位复合导电聚合物，并同时实现生物分子在聚合物复合膜中的固定。
Objective to study the collapse of biomolecules , focusing on the effect of the composition of chain , temperature and stiffness on the chains self - assembly 摘要目的研究生物分子链的自组织坍塌过程；探讨分子序列的组分、温度和链的柔性对生物分子自组织过程的影响。
We use the methods of chemical modifications to create active basal molecules on the matrix surface of electrodes and successfully immobilize the biomolecules onto the matrix 我们应用化学修饰的方法，使电极基片表面产生活泼基团，从而成功地将生物分子(抗原)固定在基片上。
The most commonly used method for the covalent binding of biomolecules onto 1 - d nanostructures is through the diimide - activated amidation of carboxylic acid terminated nanostructures 最常用的方法是通过端羧酸基纳米结构的二酰亚胺活化氨基化合物来进行生物分子与1 - d纳米结构的共价结合。
In this paper , monolayer , microemulsion and biomolecule were selected as the template to induce crystal growth of calcium oxalate . the effect factors of them were discussed 本文分别选择单分子膜、微乳液、生物分子作为模板诱导草酸钙晶体生长，并探讨了促进和抑制草酸钙晶体生长的因素。
