ISM can be performed in fluorescence, bright field or interference microscopy. Several different implementations have been described, with associated advantages and disadvantages. In two-photon microscopy, the illumination and detection point spread functions are very different. This is also the case when using pupil filters or when there is a large Stokes shift.
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Colin J. R. Sheppard, Marco Castello, Giuseppe Vicidomini, Martí Duocastella, Alberto Diaspro, "Microscopy using source and detector arrays," Proc. SPIE 9713, Three-Dimensional and Multidimensional Microscopy: Image Acquisition and Processing XXIII, 971302 (9 March 2016);