The discussion centers on the maximum magnification achieved by microscopes, emphasizing the importance of resolution rather than just magnification numbers. The resolution is fundamentally limited by the wavelength of the imaging source, with visible light resolving structures down to approximately 200 nm and electron microscopes capable of imaging individual atoms. The conversation highlights that standard microscopy is diffraction-limited, but advancements in superresolution microscopy techniques, such as near-field probes and methods like PALM and STED, have enabled resolutions down to single nanometers using visible light. These techniques allow for imaging beyond traditional limits by utilizing unique properties of light and fluorescence. Additionally, the maximum useful magnification in light microscopes is roughly 1000 times the numerical aperture, while for electron microscopes, it is about 1000 times the accelerating voltage.