Fig. 1: Simultaneous spatiotemporal super-resolution and multi-parametric fluorescence microscopy from a single fluorescence data set.
From: Simultaneous spatiotemporal super-resolution and multi-parametric fluorescence microscopy
The various analyses performed on a single fluorescence data set are shown here: autocorrelation analysis to determine diffusion coefficient (top left), number and brightness analysis to determine particle brightness (top right), super-resolution radial fluctuations imaging to resolve structures (bottom left), and FCS diffusion law to determine sub-resolution protein organization (bottom right).
