背景(考古学)
四氧化锇
超微结构
荧光
染色
分辨率(逻辑)
显微镜
锇
嵌入
荧光显微镜
化学
生物物理学
生物
电子显微镜
病理
解剖
生物化学
光学
计算机科学
物理
医学
人工智能
遗传学
钌
催化作用
古生物学
作者
Zhifei Fu,Dingming Peng,Mingshu Zhang,Fudong Xue,Rui Zhang,Wenting He,Tao Xu,Pingyong Xu
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2019-10-14
卷期号:17 (1): 55-58
被引量:73
标识
DOI:10.1038/s41592-019-0613-6
摘要
Super-resolution correlative light and electron microscopy (SR-CLEM) is a powerful approach for imaging specific molecules at the nanoscale in the context of the cellular ultrastructure. Epon epoxy resin embedding offers advantages for SR-CLEM, including ultrastructural preservation and high quality sectioning. However, Epon embedding eliminates fluorescence from most fluorescent proteins. We describe a photocontrollable fluorescent protein, mEosEM, that can survive Epon embedding after osmium tetroxide (OsO4) treatment for improved SR-CLEM.
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