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A simple method for the removal of glass coverslips from flat-embedded cultured cells for transmission electron microscopy.

作者信息

Howell A S, Sharma S, Notter M F, Hansen J T

机构信息

Department of Neurobiology and Anatomy, University of Rochester Medical Center, NY 14642.

出版信息

J Electron Microsc Tech. 1988 Feb;8(2):239-40. doi: 10.1002/jemt.1060080217.

DOI:10.1002/jemt.1060080217
PMID:3073200
Abstract
摘要

相似文献

1
A simple method for the removal of glass coverslips from flat-embedded cultured cells for transmission electron microscopy.一种用于从平板包埋的培养细胞中移除盖玻片以进行透射电子显微镜检查的简单方法。
J Electron Microsc Tech. 1988 Feb;8(2):239-40. doi: 10.1002/jemt.1060080217.
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Simple devices for the preparation of specimens for scanning and transmission electron microscopy.用于制备扫描和透射电子显微镜标本的简易装置。
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The effects of fixation, dehydration and critical point drying on the size of cultured smooth muscle cells.固定、脱水和临界点干燥对培养的平滑肌细胞大小的影响。
Scan Electron Microsc. 1979(3):439-48.
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A convenient method for in situ processing of cultured cells for cytochemical localization by electron microscopy.
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Improved methods for using glass coverslips in cell culture and electron microscopy.细胞培养和电子显微镜检查中使用玻璃盖玻片的改进方法。
J Histochem Cytochem. 1992 Jun;40(6):875-7. doi: 10.1177/40.6.1588032.
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A simple and cheap method for removing glass coverslips from neuronal cultures and relocating identified cells.一种从神经元培养物中移除玻璃盖玻片并重新定位已识别细胞的简单且廉价的方法。
J Neurosci Methods. 1983 Jan;7(1):67-71. doi: 10.1016/0165-0270(83)90020-1.
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Preparation of cultured mammalian cells for transmission and scanning electron microscopy using Aclar film.使用Aclar膜制备用于透射和扫描电子显微镜的培养哺乳动物细胞。
J Electron Microsc Tech. 1988 Sep;10(1):77-85. doi: 10.1002/jemt.1060100110.
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A method for electron microscopic preparation of cultured cells (monolayer) in a new test chamber (TCSC-1).
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Epoxy-slide embedment of cytochemically stained tissues and cultured cells for light and electron microscopy.
Stain Technol. 1986 Jan;61(1):51-8. doi: 10.3109/10520298609110706.
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An improved method for embedding with Quetol 651 and ERL 4206 for stereoscopic observation of thick sections under 400 kV transmission electron microscope.一种用喹托651和ERL 4206进行包埋的改进方法,用于在400 kV透射电子显微镜下对厚切片进行立体观察。
J Electron Microsc (Tokyo). 1987;36(3):133-5.

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Rodent and primate adrenal medullary cells in vitro: phenotypic plasticity in response to coculture with C6 glioma cells or NGF.啮齿动物和灵长类动物肾上腺髓质细胞的体外培养:与C6胶质瘤细胞或神经生长因子共培养时的表型可塑性
Exp Brain Res. 1989;76(1):38-46. doi: 10.1007/BF00253621.