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Titlebook: Methods of Preparation for Electron Microscopy; An Introduction for David G. Robinson,Ulrich Ehlers,Friedrich-Wilhelm Book 1987 Springer-

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发表于 2025-3-21 19:27:25 | 显示全部楼层 |阅读模式
书目名称Methods of Preparation for Electron Microscopy
副标题An Introduction for
编辑David G. Robinson,Ulrich Ehlers,Friedrich-Wilhelm
视频video
图书封面Titlebook: Methods of Preparation for Electron Microscopy; An Introduction for  David G. Robinson,Ulrich Ehlers,Friedrich-Wilhelm  Book 1987 Springer-
描述In 1939, when the electron optics laboratory of Siemens & Halske Inc. began to manufacture the first electron microscopes, the biological and medical profes­ sions had an unexpected instrument at their disposal which exceeded the reso­ lution of the light microscope by more than a hundredfold. The immediate and broad application of this new tool was complicated by the overwhelming prob­ lems inherent in specimen preparation for the investigation of cellular struc­ tures. The microtechniques applied in light microscopy were no longer appli­ cable, since even the thinnest paraffin layers could not be penetrated by electrons. Many competent biological and medical research workers expressed their anxiety that objects in high vacuum would be modified due to complete dehydration and the absorbed electron energy would eventually cause degrada­ tion to rudimentary carbon backbones. It also seemed questionable as to whether it would be possible to prepare thin sections of approximately 0. 5 11m from heterogeneous biological specimens. Thus one was suddenly in posses­ sion of a completely unique instrument which, when compared with the light microscope, allowed a 10-100-fold higher resolutio
出版日期Book 1987
关键词Thin section; antibody; cell; cell culture; electron microscopy; electron optics; microscopy; nucleic acid;
版次1
doihttps://doi.org/10.1007/978-3-642-48848-1
isbn_softcover978-3-540-17592-6
isbn_ebook978-3-642-48848-1
copyrightSpringer-Verlag Berlin Heidelberg 1987
The information of publication is updating

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Methods for TEM,.1.6) special pieces of equipment are not necessary: all that is needed is a bench centrifuge and normal laboratory glassware. The fixatives which are in general use are both poisonous and volatile, which means that (1) solutions should not be mouth-pipetted, (2) one works, whenever possible, in a f
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David G. Robinson Ph.D.,Ulrich Ehlers,Rainer Herken,Bernd Herrmann,Frank Mayer,Friedrich-Wilhelm Schditions as well as a considerable amount of completely new m.As our understanding of G protein-coupled receptor (GPCR) signal transduction continues to grow, we cannot help but be struck by the emerging complexity and the ability of this receptor superfamily to continually surprise us as new facets
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David G. Robinson Ph.D.,Ulrich Ehlers,Rainer Herken,Bernd Herrmann,Frank Mayer,Friedrich-Wilhelm Schity and the ability of this receptor superfamily to continually surprise us as new facets are discovered. In this third edition of .Receptor Signal Transduction Protocols., the expert contributors have taken into account the constant evolution of the GPCR field and dealt with methods that allow rese
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ity and the ability of this receptor superfamily to continually surprise us as new facets are discovered. In this third edition of .Receptor Signal Transduction Protocols., the expert contributors have taken into account the constant evolution of the GPCR field and dealt with methods that allow rese
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