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標(biāo)題: Titlebook: Biological Low-Voltage Scanning Electron Microscopy; Heide Schatten,James B. Pawley Book 2008 Springer-Verlag New York 2008 biology.cell.c [打印本頁]

作者: 叛亂分子    時(shí)間: 2025-3-21 19:29
書目名稱Biological Low-Voltage Scanning Electron Microscopy影響因子(影響力)




書目名稱Biological Low-Voltage Scanning Electron Microscopy影響因子(影響力)學(xué)科排名




書目名稱Biological Low-Voltage Scanning Electron Microscopy網(wǎng)絡(luò)公開度




書目名稱Biological Low-Voltage Scanning Electron Microscopy網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Biological Low-Voltage Scanning Electron Microscopy被引頻次




書目名稱Biological Low-Voltage Scanning Electron Microscopy被引頻次學(xué)科排名




書目名稱Biological Low-Voltage Scanning Electron Microscopy年度引用




書目名稱Biological Low-Voltage Scanning Electron Microscopy年度引用學(xué)科排名




書目名稱Biological Low-Voltage Scanning Electron Microscopy讀者反饋




書目名稱Biological Low-Voltage Scanning Electron Microscopy讀者反饋學(xué)科排名





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https://doi.org/10.1007/978-3-8351-9105-1eam energy of 5 keV or lower, offers significant improvements in the lateral and depth spatial resolution compared to conventional beam energy operation of 10 keV and higher. This improvement must be offset against the limitations that the low-beam energy imposes upon analytical x-ray spectrometry.
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作者: Aggressive    時(shí)間: 2025-3-23 05:54
High-Resolution, Low Voltage, Field-Emission Scanning Electron Microscopy (HRLVFESEM) Applications chapter are 1) Visualization of sub-membranous cytoskeletal features using cytoskeleton stabilization and membrane extraction protocols. Two examples of different specimens in this section are (1.1) subpellicular cytoskeletal structures of the apicomplexan parasite ., and (1.2) submembraneous actin
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作者: cringe    時(shí)間: 2025-3-23 13:51
Developments in Instrumentation for Microanalysis in Low-Voltage Scanning Electron Microscopy,ured may become practically inaccessible at concentrations below 0.1 mass fraction, or even higher. New developments in x-ray spectrometry techniques, including optic-augmented wavelength-dispersive spectrometry and microcalorimeter energy-dispersive x-ray spectrometry, will improve the analysis sit
作者: 推遲    時(shí)間: 2025-3-23 18:29
lications of FESEM in biological samples. It provides a comprehensive explanation of instrumentation, applications, and protocols, and is intended to teach the reader how to operate such microscopes to obtain the best quality images..978-1-4899-9584-1978-0-387-72972-5
作者: critique    時(shí)間: 2025-3-24 01:30
https://doi.org/10.1007/978-3-8348-9277-5 chapter are 1) Visualization of sub-membranous cytoskeletal features using cytoskeleton stabilization and membrane extraction protocols. Two examples of different specimens in this section are (1.1) subpellicular cytoskeletal structures of the apicomplexan parasite ., and (1.2) submembraneous actin
作者: molest    時(shí)間: 2025-3-24 04:22
https://doi.org/10.1007/978-3-8351-9105-1 method developed specifically for frozen-hydrated bulk samples: doublelayer coating. In this approach, the frozen sample is coated in a manner similar to that used to produce a TEM-replica, e.g., with a shadow of platinum (at an angle of 45°) followed by an additional layer of carbon. The sample is
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Molecular Labeling for Correlative Microscopy: LM, LVSEM, TEM, EF-TEM and HVEM,
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Biological Low-Voltage Scanning Electron Microscopy978-0-387-72972-5
作者: FILTH    時(shí)間: 2025-3-25 15:32
High-Resolution, Low Voltage, Field-Emission Scanning Electron Microscopy (HRLVFESEM) Applications permitted novel and powerful applications for cell biology, as it allows detailed insights into small biological features due to the minimal coating requirements. It allows resolution at levels that previously could only be achieved with transmission electron microscopy (TEM) and it has made it poss
作者: Jejune    時(shí)間: 2025-3-25 19:43
High-Resolution Cryoscanning Electron Microscopy of Biological Samples, It circumvents artifact formation caused by chemical fixation and drying. Cryofixation is preferentially done by high-pressure freezing because it allows for fixation of native samples up to 200 μm thick and 2mm wide with minimal or no ice crystal damage. Because in the SEM only the surface of the
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