Researchers in Prof. Karl Deisseroth's laboratory have patented a revolutionary technique that can be utilized to map neural circuits in the whole brain.
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 at the Kasevich Lab have developed a module that can attach to any standard optical system or sensor for wide-field, time-resolved imaging.
Stanford researchers have proposed a novel, in vivo, real-time epifluorescence imaging method in the second near-infrared region using single-walled carbon nanotubes (SWNTs).
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).
Stanford researchers have developed a lanthanide-doped upconverting nanoparticle (UCNP) that emits very photostable and non-blinking light, and is bright enough to delineate tumor boundaries to the naked eye during surgery.
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.
Stanford researchers patented a method to design, computationally optimize and fabricate efficient optical devices using semiconducting and dielectric nanostructures.
Researchers in Prof. Karl Deisseroth's laboratory have developed a highly precise, scalable optical system for imaging or controlling thousands of individual neurons in the 3D volume accessible with a single multiphoton fluorescent microscope objective.
Researchers in Prof. Karl Deisseroth's laboratory have engineered a cytosolic, red genetically encoded calcium indicator (GECI) with high signal change at single cell resolution.
Stanford researchers at the Rao Lab have developed apoptosis imaging probes with an improved new molecular structure enabling high sensitivity and stability with better performance in vivo.
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.
Researchers at the Solgaard Lab have demonstrated that light sheet fluorescence microscopy (LSFM) with structured and pivoting illumination enables fast image acquisition and improved image quality.