Analysis of heterogeneous interactions.
作者信息
Cole James L
机构信息
Department of Molecular and Cell Biology, University of Connecticut, Storrs, Connecticut 06269, USA.
出版信息
Methods Enzymol. 2004;384:212-32. doi: 10.1016/S0076-6879(04)84013-8.
Abstract
摘要
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本文引用的文献
1
Analytical ultracentrifugation as a contemporary biomolecular research tool.分析型超速离心法作为一种当代生物分子研究工具。
J Biomol Tech. 1999 Dec;10(4):163-76.
2
Measuring protein-protein interactions by equilibrium sedimentation.通过平衡沉降法测量蛋白质-蛋白质相互作用。
Curr Protoc Immunol. 2007 Nov;Chapter 18:18.8.1-18.8.28. doi: 10.1002/0471142735.im1808s79.
3
Calculating sedimentation coefficient distributions by direct modeling of sedimentation velocity concentration profiles.通过沉降速度浓度分布的直接建模计算沉降系数分布
Methods Enzymol. 2004;384:185-212. doi: 10.1016/S0076-6879(04)84012-6.
4
Analysis of heterologous interacting systems by sedimentation velocity: curve fitting algorithms for estimation of sedimentation coefficients, equilibrium and kinetic constants.通过沉降速度分析异源相互作用系统：用于估算沉降系数、平衡常数和动力学常数的曲线拟合算法
Biophys Chem. 2004 Mar 1;108(1-3):231-43. doi: 10.1016/j.bpc.2003.10.028.
5
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6
Applications of calorimetric methods to drug discovery and the study of protein interactions.量热法在药物发现及蛋白质相互作用研究中的应用。
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7
Recent advances in fluorescence correlation spectroscopy.荧光相关光谱学的最新进展。
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8
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9
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Comparative assessment of large-scale data sets of protein-protein interactions.蛋白质-蛋白质相互作用大规模数据集的比较评估。
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