Abstract
Methods to simultaneously localize the positions of multiple single fluorophores by precisely determining their individual positions are now yielding impressive gains in fluorescence microscopy resolution.
MeSH terms
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Cells / chemistry*
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Cells / ultrastructure*
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Fluorescent Dyes
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Imaging, Three-Dimensional / methods*
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Microscopy, Fluorescence / methods
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Nanotechnology / methods*
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Proteins / chemistry*
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Sensitivity and Specificity
Substances
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Fluorescent Dyes
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Proteins