The second is the study on the influence of dynamical effects in quantitative electron crystallography.
其二是对动力学效应在定量电子晶体学中的影响的研究。
Protein electron crystallography is now able to measure the three-dimensional structure of membrane proteins at atomic resolution.
蛋白质电子晶体学已能以原子分辨率解析膜蛋白三维结构。
The fundamental, method and deficiency of quantitative electron crystallography have been described, further improvement for it was discussed.
阐述了定量电子晶体学测定晶体电荷密度分布的基本原理和方法、不足之处和改善途径。
Two dimensional crystallization of membrane proteins is the base on which their three dimensional structure are solved by electron crystallography.
膜蛋白的二维结晶化是蛋白质电子晶体学解析膜蛋白三维结构的基础。
In this paper, some recent developments of electron crystallography and its applications in structure determination of inorganic crystals in the past decade are shown.
本文将概括地介绍最近十几年中电子晶体学的一些最新进展及其在无机晶体结构解析方面的一些最新应用实例。
However, compared to X-ray crystallography, electron crystallography confronts with a critical problem, i. e. dynamical diffraction problem which makes structure analysis very complicated.
然而,由于电子与晶体之间强烈的动力学交互作用,使得用电子显微镜方法分析结构复杂化。
Currently, the main methodologies for high-resolution protein structure determination in experimentation have been available, such as X-ray crystallography, NMR, electron microscopy etc.
实验上研究蛋白质结构的主要手段有X射线晶体学技术、核磁共振衍射技术、电子纤维技术等。
The morphology and crystallography analysis of lath martensite within a packet in 17CrNiMo6 steel was studied by electron backscattering diffraction(EBSD) with field emission gun.
利用电子背散射衍射(EBSD)技术和TEM分析方法研究了17CrNiMo6钢中一个形态上的packet内的板条马氏体的形态与晶体学特征。
The morphology and crystallography analysis of lath martensite within a packet in 17CrNiMo6 steel was studied by electron backscattering diffraction(EBSD) with field emission gun.
利用电子背散射衍射(EBSD)技术和TEM分析方法研究了17CrNiMo6钢中一个形态上的packet内的板条马氏体的形态与晶体学特征。
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