This technology is an imaging method that uses a spacer for high resolution and a relatively large field of view for real-time imaging of live specimens.
There has been great interest in the development of microscopy technologies to study the cellular function and structure of model organisms. While there have been great advancements in three-dimensional (3D) imaging and microscopy tools, current methods are limited in their ability to perform real-time imaging with high resolution of 3D specimens.
This technology is a swept, confocally aligned planar excitation (SCAPE) microscopy method that uses a spacer for an immersion objective lens using a UV-curable polymer, which allows for fast volumetric imaging of living samples. Included in this method are optical components, a scanning element, alignment mirrors, and a plurality of light sources that each have output beams for their respective wavelengths. This SCAPE method has increased high-throughput volumetric imaging with a wide range of view of many tissue types across model organisms such as the live mouse brain, whole drosophila embryos, adult C. elegans, and whole bodies of zebrafish larvae. In addition to time imaging of live specimens, this technology can also be customizable depending on research needs.
Elizabeth M. C. Hillman, Ph.D.
Patent Pending(US20230408803)
IR CU21199, CU21251
Licensing Contact: Kristin Neuman
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