Stanford researchers have developed a device that combines one-photon and two-photon microscopy using fast temporal multiplexing enabling 3D alignment between in vivo and ex vivo data for neuroscience and spatial biology applications.
Stanford researchers designed and built a light sheet microscope that can be used for deconvolution-free, high resolution volumetric imaging of cleared tissue specimens.
Researchers at Stanford have developed methods for evaluating the position of a micro-electromechanical system (MEMS) device in terms of phase and/or amplitude characteristics.
Stanford researchers at the Prakash Lab have developed Octopi, a low-cost ($250-$500) and reconfigurable autonomous microscopy platform capable of automated slide scanning and correlated bright-field and fluorescence imaging.
Stanford researchers at the Kasevich Lab have developed a module that can attach to any standard optical system or sensor for wide-field, time-resolved imaging.
Researchers in Prof. Mark Schnitzer's laboratory have developed a two-photon scanning microscope for imaging neural activity in a 2x2mm field of view while maintaining a fast scanning rate (~10Hz image update frequency).
Researchers in Prof. W.E. Moerner's laboratory have developed a compact point spread function (PSF) that enables optical imaging in three dimensions with nanoscale precision using a limited number of photons.
Stanford researchers have designed a tunable wedge-based phase mask for 3D super-resolution imaging that can simultaneously determine both the position and rotational mobility of individual light-emitting molecules from a single camera image.
An interdisciplinary team of Stanford researchers is developing a dual axis confocal (“DAC”) microscope system for in vivo imaging of tissues at the cellular scale.
Stanford researchers have developed an ultrafast multi-foci two-photon microscope system that aims at 1 kHz full frame rate with 500x500 ?m2 field of view (FOV). It utilizes a 2D foci-array pattern and 1D scanning mechanism to achieve full FOV excitation coverage.
Precision in surgical removal of cancer is guided by pathological assessment of resected tissues, and there is a dire need to reduce the time and distance between the critical diagnostic events and the surgical procedure.