2013
DOI: 10.1007/978-1-62703-776-1_1
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Conventional Specimen Preparation Techniques for Transmission Electron Microscopy of Cultured Cells

Abstract: In this chapter, we discuss conventional methods for handling cells grown suspended in liquid culture and on solid substrates. Protocols are given on how to prepare cultures for transmission electron microscopy, including the most commonly used buffers, fixatives, enrobement media, and embedding resins. These methods are suitable for a wide variety of organisms, ranging from prokaryotic bacteria to mammalian cells.

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Cited by 57 publications
(66 citation statements)
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“…A detailed protocol was followed as previously described by Bozzola with minimal modification (41). Ultrathin sections were post-stained and examined using a Hitachi transmission electron microscope.…”
Section: Methodsmentioning
confidence: 99%
“…A detailed protocol was followed as previously described by Bozzola with minimal modification (41). Ultrathin sections were post-stained and examined using a Hitachi transmission electron microscope.…”
Section: Methodsmentioning
confidence: 99%
“…The obtained data were analyzed using ANOVA and Post Hoc test. Significant P value was set at 0.05 (12).…”
Section: Quantitative Evaluation For the Immunostained Sectionsmentioning
confidence: 99%
“…Strain typing was performed by pulsed-field gel electrophoresis (PFGE) as described by Mannu and Paba (2002). In addition, scanning electron microscopy (SEM) was performed on strains with a Zeiss DSM962 microscopy (Bozzola, 2007).…”
Section: Isolates Identification and Strain Typingmentioning
confidence: 99%