WAVEFRONT CONTROL FOCUS around 1550 wavenumbers formed a tighter focus and enhanced spectra from the surrounding brain tissue.
A key benefit of using AO in confocal Raman microscopy is speed: Raman measurements can
Figure 2. AO in multi-photon excitation microscopy. The microscope uses the combined energy of multiple incident NIR photons to excite a fluorescence process. The use of Megapixel SLMs allows to compensate complex aberration patterns, causing strong signal enhancements. The images on the top show images of microglial cells expressing green fluorescent protein in fixed mouse brain tissue at about 200 µ m depth. The images on the bottom demonstrate the imaging of microbeads through 500 µ m of chicken breast tissue.
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