Double staining method for array tomography using scanning electron microscopy

Abstract Scanning electron microscopy (SEM) plays a central role in analyzing structures by imaging a large area of brain tissue at nanometer scales. A vast amount of data in the large area are required to study structural changes of cellular organelles in a specific cell, such as neurons, astrocyte...

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Main Authors: Eunjin Kim, Jiyoung Lee, Seulgi Noh, Ohkyung Kwon, Ji Young Mun
Format: Article
Language:English
Published: SpringerOpen 2020-06-01
Series:Applied Microscopy
Subjects:
Online Access:https://doi.org/10.1186/s42649-020-00033-8
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spelling doaj-0dbac22035b549178c83159b6cf2e0602021-06-27T11:25:39ZengSpringerOpenApplied Microscopy2287-44452020-06-015011610.1186/s42649-020-00033-8Double staining method for array tomography using scanning electron microscopyEunjin Kim0Jiyoung Lee1Seulgi Noh2Ohkyung Kwon3Ji Young Mun4National Instrumentation Center for Environmental Management, Seoul National UniversityNational Instrumentation Center for Environmental Management, Seoul National UniversityDepartment of Brain and Cognitive Sciences, Daegu Gyeongbuk Institute of Science & Technology (DGIST)National Instrumentation Center for Environmental Management, Seoul National UniversityNeural circuit research group, Korea Brain Research InstituteAbstract Scanning electron microscopy (SEM) plays a central role in analyzing structures by imaging a large area of brain tissue at nanometer scales. A vast amount of data in the large area are required to study structural changes of cellular organelles in a specific cell, such as neurons, astrocytes, oligodendrocytes, and microglia among brain tissue, at sufficient resolution. Array tomography is a useful method for large-area imaging, and the osmium-thiocarbohydrazide-osmium (OTO) and ferrocyanide-reduced osmium methods are commonly used to enhance membrane contrast. Because many samples prepared using the conventional technique without en bloc staining are considered inadequate for array tomography, we suggested an alternative technique using post-staining conventional samples and compared the advantages.https://doi.org/10.1186/s42649-020-00033-8Array tomographyDouble staining with uranyl acetate and leadScanning electron microscopy
collection DOAJ
language English
format Article
sources DOAJ
author Eunjin Kim
Jiyoung Lee
Seulgi Noh
Ohkyung Kwon
Ji Young Mun
spellingShingle Eunjin Kim
Jiyoung Lee
Seulgi Noh
Ohkyung Kwon
Ji Young Mun
Double staining method for array tomography using scanning electron microscopy
Applied Microscopy
Array tomography
Double staining with uranyl acetate and lead
Scanning electron microscopy
author_facet Eunjin Kim
Jiyoung Lee
Seulgi Noh
Ohkyung Kwon
Ji Young Mun
author_sort Eunjin Kim
title Double staining method for array tomography using scanning electron microscopy
title_short Double staining method for array tomography using scanning electron microscopy
title_full Double staining method for array tomography using scanning electron microscopy
title_fullStr Double staining method for array tomography using scanning electron microscopy
title_full_unstemmed Double staining method for array tomography using scanning electron microscopy
title_sort double staining method for array tomography using scanning electron microscopy
publisher SpringerOpen
series Applied Microscopy
issn 2287-4445
publishDate 2020-06-01
description Abstract Scanning electron microscopy (SEM) plays a central role in analyzing structures by imaging a large area of brain tissue at nanometer scales. A vast amount of data in the large area are required to study structural changes of cellular organelles in a specific cell, such as neurons, astrocytes, oligodendrocytes, and microglia among brain tissue, at sufficient resolution. Array tomography is a useful method for large-area imaging, and the osmium-thiocarbohydrazide-osmium (OTO) and ferrocyanide-reduced osmium methods are commonly used to enhance membrane contrast. Because many samples prepared using the conventional technique without en bloc staining are considered inadequate for array tomography, we suggested an alternative technique using post-staining conventional samples and compared the advantages.
topic Array tomography
Double staining with uranyl acetate and lead
Scanning electron microscopy
url https://doi.org/10.1186/s42649-020-00033-8
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