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A more recent method of light sheet microscopy that is mostly employed in biological settings is lattice light sheet microscopy. It is a technique that makes use of sheets of light arranged in a lattice configuration to fluoresce samples and cause images and videos to be captured.
By illuminating the cell, tissue, or organism one slice at a time with thin sheets of light, lattice light-sheet microscopy overcomes this difficulty and minimizes exposure to harsh laser light. Because of this, the method has very little phototoxicity or photobleaching effects and is gentle on live samples.
Light-sheet microscopy has a variety of uses, including the rapid inter- and intracellular processes and imaging of subcellular structures, as well as the long-term development of model systems and the full visualisation of a macroscale cleared sample. Ions form the bulk of an ionic compound.
The ions are organised into a regular, repeating structure known as an ionic lattice. Because the ions are attracted to one another and arrange themselves in a predictable pattern with oppositely charged ions next to one another, a lattice is created.
Global lattice light sheet Microscopy Market accounted for $XX Billion in 2023 and is anticipated to reach $XX Billion by 2030, registering a CAGR of XX% from 2024 to 2030.
The newest version of the ZEISS Lattice Lightsheet 7 is made available by ZEISS. The microscope system, which was released to the market in December 2020, gave researchers a new avenue for examining the dynamics of life at the subcellular level.
It was the first practical, commercial application of the lattice light-sheet technology, which permits long-term imaging of living cells while preserving samples. The life science research community can now benefit from a number of advancements made to the new generation of ZEISS Lattice Lightsheet 7, which will significantly advance live cell experiment.
While safeguarding the sample from photodamage and bleaching over hours and days of continuous imaging, the system provides both an unprecedented uniform background and a strong enough signal to distinguish the tiniest subcellular structures at the lowest photon count rates.
