Subdiffraction-resolution fluorescence imaging with conventional fluorescent probes.

By M. Heilemann, S. van de Linde, M. Schüttpelz, R. Kasper, B. Seefeldt, Anindita Mukherjee, Philip Tinnefeld, Markus Sauer. Angewandte Chemie, 2008

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Mapping molecular statistics with balanced super-resolution optical fluctuation imaging (bSOFI) (2012, methodology): “…in photo-activation localization microscopy (PALM) (Betzig et al. 2006; Hess et al. 2006) and stochastic optical reconstruction microscopy (STORM) (Heilemann et al. 2008; Rust et al. 2006), or by analysing the statistics of the temporal fluctuations as exploited in super-resolution optical…”
Frontiers in structured illumination microscopy (2016, background): “Notable examples include photoactivated localization microscopy (PALM) [7], fluorescence PALM [8], stochastic optical reconstruction microscopy (STORM) [9], and direct STORM [10], with the latter also known as ground state depletion microscopy followed by individual molecule return [11].”
Evaluation of fluorophores for optimal performance in localization-based super-resolution imaging (2011, positive): “Like Alexa 647, a variety of commonly used organic dyes spanning a broad spectrum of colors can transition between fluorescent and dark states and have been used for super-resolution imaging 8,10,11,14–16 .”
Super resolution fluorescence microscopy (2009, background): “5, and Cy7 dyes can also be spontaneously activated and deactivated by the same imaging laser (23) (for example 647 nm) without the need of activators but emit light of different wavelenths ranging from red to near IR, providing the possibility of multicolor imaging by distinguishing emission color ”