| Literature DB >> 34250204 |
Haiting Yan1, Yue Wang1, Jingrong Zhang2, Xinru Cui2, Jiasong Wu2, Jie Zhou2, Yuan Chen2, Jia Lu2, Ruiyang Guo2, Maggie Ou3, Hongxu Lai4, Zhiming Yu1.
Abstract
Cryo-scanning electron microscopy (cryo-SEM) was first introduced for scientific use in the 1980s. Since then, cryo-SEM has become a routine technique for studying the surfaces and internal structures of biological samples with a high water content. In contrast to traditional SEM, cryo-SEM requires no sample pretreatment processes; thus, we can obtain the most authentic images of the sample shape and structure. Cryo-SEM has two main steps: cryoprocessing of samples and scanning electron microscopy (SEM) observation. The cryoprocessing step includes preparation of the cooled slushing station, cooling of the preparation chamber, sample preparation, and sputtering. The sample is then transferred to an SEM cold stage for observation. We used cryo-SEM to study rice root hair tissues, but the methods and protocols can be applied to other root systems. This protocol optimizes the two key operation steps of reducing the humidity in the growth chamber and previewing the samples before sputtering and can more quickly obtain high-quality images.Entities:
Keywords: Cell interior; Cryo-SEM; Density; Diameter; Mutant; Rice; Root hair
Year: 2021 PMID: 34250204 PMCID: PMC8249913 DOI: 10.21769/BioProtoc.4037
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325