Correlative confocal and scanning electron microscopy of cultured cells without using dedicated equipment

被引:3
作者
Casares-Arias, Javier [1 ,2 ,4 ]
Alonso, Miguel A. [1 ,2 ]
San Paulo, Alvaro [3 ]
Gonzalez, Maria Ujue [3 ]
机构
[1] CSIC, Ctr Biol Mol Severo Ochoa, Madrid 28049, Spain
[2] Univ Autonoma Madrid, Madrid 28049, Spain
[3] CSIC CEI UAM CSIC, Inst Micro & Nanotecnol, IMN CNM, Madrid 28760, Spain
[4] Eidgenoss TH ETH Zurich, Dept Biosyst Sci & Engn, CH-4058 Basel, Switzerland
来源
STAR PROTOCOLS | 2021年 / 2卷 / 03期
关键词
Cell Biology; Microscopy;
D O I
10.1016/j.xpro.2021.100727
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This protocol enables correlative light and electron microscopy (CLEM) imaging of cell surface features without using dedicated equipment. Cells are cultured and fixed on transparent substrates for confocal microscopy imaging. No conductive coating is employed in the scanning electron microscopy workflow, providing a clean cell surface observation, with fiducial markers assisting alignment of optical and topographical images. This protocol describes CLEM imaging for midbody remnants in MDCK cells but can also be applied to different cell types and surface features.For complete details on the use and execution of this protocol, please refer to Casares-Arias et al. (2020).
引用
收藏
页数:19
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