Two-photon excited fluorescence (2PEF) is a unique photophysical process that has benefited many diverse areas of science. Imaging the 2PEF signal offers numerous intrinsic benefits, including low background scattering, high sample photo-stability, and high excitation selectivity. The 2PEF signal has a nonlinear dependence on excitation intensity, which has proven to be extremely useful for high resolution, three dimensional microscopy. This same nonlinear dependence, in conjunction with the typically low probability of two-photons being simultaneously absorbed, also makes 2PEF imaging difficult to scale, leaving most two-photon microscopes with a field of view (FOV) limited to less than a few mm 2. This effectively limits the benefits of the unique properties of 2PEF imaging to microscopic applications. This dissertation explores the development and application of a wide FOV 2PEF imaging technique, where a FOV as large as 10 cm 2 is achieved by increasing the peak photon flux of the excitation source, and expanding the illumination region. The use of this imaging technique for the in depth characterization and optimization of fluorescent proteins (FPs), as well as taking high contrast images of fingermarks is described. This new wide FOV 2PEF imaging technique greatly expands the usefulness of the unique photophysical properties of 2PEF and allows for sensitive, high contrast 2PEF imaging on a much larger scale than was previously possible.