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用于扫描电子显微镜的免疫金标记

Immunogold Labeling for Scanning Electron Microscopy.

作者信息

Goldberg Martin W, Fišerová Jindřiška

机构信息

School of Biological and Biomedical Sciences, Durham University, South Road, Durham, DH1 3LE, UK.

Department of Biology of the Cell Nucleus, Institute of Molecular Genetics AS CR, v.v.i.,, Videnska 1083, 142 20, Prague 4, Czech Republic.

出版信息

Methods Mol Biol. 2016;1474:309-25. doi: 10.1007/978-1-4939-6352-2_20.

Abstract

Scanning electron microscopes are useful biological tools that can be used to image the surface of whole organisms, tissues, cells, cellular components, and macromolecules. Processes and structures that exist at surfaces can be imaged in pseudo, or real 3D at magnifications ranging from about 10× to 1,000,000×. Therefore a whole multicellular organism, such as a fly, or a single protein embedded in one of its cell membranes can be visualized. In order to identify that protein at high resolution, or to see and quantify its distribution at lower magnifications, samples can be labeled with antibodies. Any surface that can be exposed can potentially be studied in this way. Presented here is a generic method for immunogold labeling for scanning electron microscopy, using two examples of specimens: isolated nuclear envelopes and the cytoskeleton of mammalian culture cells. Various parameters for sample preparation, fixation, immunogold labeling, drying, metal coating, and imaging are discussed so that the best immunogold scanning electron microscopy results can be obtained from different types of specimens.

摘要

扫描电子显微镜是有用的生物学工具,可用于对整个生物体、组织、细胞、细胞成分和大分子的表面进行成像。存在于表面的过程和结构可以在约10倍至100万倍的放大倍数下以伪三维或真实三维进行成像。因此,整个多细胞生物体,如苍蝇,或嵌入其细胞膜之一的单个蛋白质都可以可视化。为了在高分辨率下识别该蛋白质,或在较低放大倍数下观察和量化其分布,可以用抗体对样品进行标记。任何可以暴露的表面都有可能以这种方式进行研究。本文介绍了一种用于扫描电子显微镜免疫金标记的通用方法,使用了两个标本示例:分离的核膜和哺乳动物培养细胞的细胞骨架。讨论了样品制备、固定、免疫金标记、干燥、金属镀膜和成像的各种参数,以便从不同类型的标本中获得最佳的免疫金扫描电子显微镜结果。

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