200 nanometer!
An ordinary optical microscope, one that forms an image with visible light and glass lenses, cannot show details smaller than about 200 nanometers, or 0.2 micrometers. A nanometer is a billionth of a meter, and a micrometer is a millionth of a meter. This limit comes from the way light behaves as a wave, and it is approximate.
The limit is on resolution: the shortest distance between two points that a microscope can still show as separate. Two points closer together than that blur into one. The limit does not depend on magnification. Beyond about 1,000 times, magnifying the image further makes it larger but shows no more detail.
In 1873, the microscopist Ernst Abbe published an equation showing that resolution depends on the wavelength of the light. In the best case, it is about half the wavelength. One common form of the calculation divides the wavelength by twice the numerical aperture, a number that measures how much light the lens gathers.
The best lenses look through a drop of oil and reach a numerical aperture of about 1.4. With green light, 550 nanometers long, they can resolve details about 0.2 micrometers apart. With red light, 700 nanometers long, the same kind of calculation gives a coarser limit, and with violet light a finer one.
The limit is on detail, not on detecting something at all. A single molecule that glows can show up in an ordinary microscope as a spot of light, if it is more than 0.2 micrometers from any other glowing molecule. The spot is blurred to the size of the limit, so it reveals where the molecule is but not what it looks like.
Shorter wavelengths give finer detail. Microscopes that use near-ultraviolet light can resolve smaller details than those using visible light. Electron microscopes go much further. The electrons they use behave as waves with a wavelength of about 0.005 nanometers, far shorter than that of light.
For most of the 20th century, scientists believed that optical microscopes could never show anything smaller than about 0.2 micrometers. Stefan Hell proposed a way around the limit in 1994 and showed it working in 2000. His method uses one pulse of light to make molecules glow and a second, ring-shaped laser beam to switch off all but those in a tiny spot.
W. E. Moerner and Eric Betzig developed another method, which switches on only a few glowing molecules at a time and combines many images. The three shared the 2014 Nobel Prize in Chemistry "for the development of super-resolved fluorescence microscopy". In the words of the Royal Swedish Academy of Sciences, which awards the prize, their work means that "microscopy has become nanoscopy".