Science Advances · 2020 · 97 citations · 29 references
Immunocytochemical TechniqueEngineeringMicroscopyMolecular BiologyBiomedical EngineeringSuper-resolution MicroscopySuper-resolution ImagingMicroscopy MethodLight MicroscopyBiophysicsNovel Imaging MethodFluorescence ImagingSuper-resolutionCell BiologySingle-molecule DetectionAbundant Reactive EntitiesFluorescence MicroscopyRobust StainsBiomedical ImagingFeature-rich Covalent StainsMedicine
Fluorescence microscopy is a workhorse tool in biomedical imaging but often poses substantial challenges to practitioners in achieving bright or uniform labeling. In addition, while antibodies are effective specific labels, their reproducibility is often inconsistent, and they are difficult to use when staining thick specimens. We report the use of conventional, commercially available fluorescent dyes for rapid and intense covalent labeling of proteins and carbohydrates in super-resolution (expansion) microscopy and cleared tissue microscopy. This approach, which we refer to as Fluorescent Labeling of Abundant Reactive Entities (FLARE), produces simple and robust stains that are modern equivalents of classic small-molecule histology stains. It efficiently reveals a wealth of key landmarks in cells and tissues under different fixation or sample processing conditions and is compatible with immunolabeling of proteins and in situ hybridization labeling of nucleic acids.
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iDISCO: A Simple, Rapid Method to Immunolabel Large Tissue Samples for Volume Imaging
Nicolas Renier, Zhuhao Wu, David Simon et al. · Cell · 2014 · 1.8K citations · Full text
Immunocytochemical Technique, Engineering, Tissue Imaging +11
Fei Chen, Paul W. Tillberg, Edward S. Boyden · Science · 2015 · 1.5K citations · Full text
Bernhard Lehnertz, Yoshihide Ueda, Alwin A.H.A. Derijck et al. · Current Biology · 2003 · 1.2K citations · Full text
Global, quantitative and dynamic mapping of protein subcellular localization
Daniel N. Itzhak, Stefka Tyanova, Jürgen Cox et al. · eLife · 2016 · 645 citations · Full text