Sprache: Englisch
Verlag: Berlin ; Heidelberg ; New York ; London ; Paris ; Tokyo : Springer, 1987
ISBN 10: 354017592X ISBN 13: 9783540175926
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Zustand: Gut. XVII, 190 S. : 62 Ill., graph. Darst. Gebraucht; Einband minimal berieben, ansonten guter Zustand. Aus dem Inhalt: An Introduction to Electron Microscops (EM) / Methods for TEM / Methods for SEM / Evaluation of Micrographs / Appendix: Buffers in Electron Microscopy / Subject Index. Sprache: Englisch Gewicht in Gramm: 350.
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Sprache: Englisch
Verlag: New York, American Elsevier Publishing, 1985
ISBN 10: 0444807012 ISBN 13: 9780444807014
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Sprache: Englisch
Verlag: Springer Berlin Heidelberg, 1987
ISBN 10: 354017592X ISBN 13: 9783540175926
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Taschenbuch. Zustand: Neu. Methods of Preparation for Electron Microscopy | An Introduction for the Biomedical Sciences | David G. Robinson (u. a.) | Taschenbuch | xviii | Englisch | 1987 | Springer | EAN 9783540175926 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.
Sprache: Englisch
Verlag: Springer Berlin Heidelberg, 1987
ISBN 10: 354017592X ISBN 13: 9783540175926
Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
Taschenbuch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - 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 resolution, yet a suitable preparation methodology was lacking. This sceptical attitude towards the application of electron microscopy in bi ology and medicine was supported simultaneously by the general opinion of colloid chemists, who postulated that in the submicroscopic region of living structures no stable building blocks existed which could be revealed with this apparatus.
Sprache: Englisch
Verlag: Elsevier Science Publishing Co Inc.,U.S., 1973
ISBN 10: 0720442524 ISBN 13: 9780720442526
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Zustand: Sehr gut. Zustand: Sehr gut | Sprache: Englisch | Produktart: Bücher | Keine Beschreibung verfügbar.
Sprache: Englisch
Verlag: Springer Berlin Heidelberg Jun 1987, 1987
ISBN 10: 354017592X ISBN 13: 9783540175926
Anbieter: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Deutschland
Taschenbuch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -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 resolution, yet a suitable preparation methodology was lacking. This sceptical attitude towards the application of electron microscopy in bi ology and medicine was supported simultaneously by the general opinion of colloid chemists, who postulated that in the submicroscopic region of living structures no stable building blocks existed which could be revealed with this apparatus. 212 pp. Englisch.
Sprache: Englisch
Verlag: Springer, Springer Jun 1987, 1987
ISBN 10: 354017592X ISBN 13: 9783540175926
Anbieter: buchversandmimpf2000, Emtmannsberg, BAYE, Deutschland
Taschenbuch. Zustand: Neu. This item is printed on demand - Print on Demand Titel. Neuware -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 resolution, yet a suitable preparation methodology was lacking. This sceptical attitude towards the application of electron microscopy in bi ology and medicine was supported simultaneously by the general opinion of colloid chemists, who postulated that in the submicroscopic region of living structures no stable building blocks existed which could be revealed with this apparatus.Springer-Verlag KG, Sachsenplatz 4-6, 1201 Wien 212 pp. Englisch.
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Buch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - While new discoveries have led to much dramatic growth in cryo-electron microscopy, researchers will never be able to take full advantage if they lack access to the details that make these techniques understandable and applicable.The Handbook of Cryo-Preparation Methods for Electron Microscopy provides researchers with a complete reference that will show them how to equip their labs with the right materials and methods to take full advantage of the latest advances. This pioneering work brings together a group of internationally renowned researchers, some the very inventors of the methods they describe, to share their knowledge and recipes. Taking care to explain the history behind the techniques and to demonstrate their use, this book presents the latest theory, principles, and protocols supplemented by hundreds of illustrations.Contributions to this handbookÖ Describe cryo-methods aimed at perfect preservation for fine structural analysisÖ Teach how to arrest physiological processes by cryo-fixationÖ Reveal the secrets for high-resolution snapshots of life by CEMOVISÖ Cover applications of cryo-methods such as electron crystallography, 2D/3D structure analysis, protein localization, and cryo-electron tomographyÖ Demonstrate the use of vitreous water as an intermediate step for localization of biological ions and moleculesÖ Present hybrid methods of freeze-substitution and freeze-drying for immunolabeling and determining molecular geographyÖ Illustrate freeze-fracture, cryo-ultramicrotomy, and resin embeddingÖ Highlight the Tokuyasu method and the new rehydration technique for highly efficient immunolabelingÖ Include summary tables to compare and obtain appropriate criteriaIncludes a wealth of immediate reference material for daily useWith clear, step-by-step recipes and lists of tools, ingredients, and suppliers, this handbookprovides researchers with the knowledge and techniques to adopt the latest cryo-methods to their current research.