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Sola led light engine

Manufactured by Hamamatsu Photonics

The SOLA LED light engine is a high-performance illumination source developed by Hamamatsu Photonics. It utilizes LED technology to provide a stable, uniform, and adjustable light output for various laboratory and scientific applications. The core function of the SOLA LED light engine is to generate and deliver controlled, consistent light for experimentation, analysis, and imaging purposes.

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3 protocols using sola led light engine

1

Multichannel Microscopy Imaging Protocol

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Three stained sections from each sample were imaged at 10x magnification within 36 hours of staining (except for sample C, which had unacceptable artefact in one section in round 1). Whole-section multichannel images were captured using a Nikon Ti2-E motorized microscope with a Lumencor SOLA LED light engine (at 50% power), a Hamamatsu ORCA Fusion camera (in 16-bit ultra-quiet mode), and Nikon Plan Apochromat Lambda objectives. Final image resolution was 0.64 μm/pixel.
All exposures were chosen by the trained operators based on best microscopy practices of avoiding signal saturation while maximizing the useful range of intensity values detected by the camera in healthy control samples. Identical imaging settings were used for all sections within the same round of staining and imaging. Operators selected exposures independently in rounds 1 and 2, which approximates the degree of variation that is likely to arise between images collected in different laboratories using different microscopy equipment. For round 3, the imaging operator was required to use the same exposure settings as those used in round 1.
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2

Wide-field Fluorescence Imaging of Skeletal Muscle and Hearts

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Whole-section multichannel wide-field fluorescence images were collected on a Nikon Ti2-E motorized microscope with a Lumencor SOLA LED light engine at 50% power and a Hamamatsu ORCA Fusion camera in 16-bit ultra-quiet mode. A 10x objective (Plan Apo λ 10x, NA 0.45, final resolution 0.65 μm/pixel) was used for skeletal muscles and a 20x objective (Plan Apo λ 20x, NA 0.75, final resolution 0.32 μm/pixel) was used for hearts. Exposure times were chosen to maximize the range of intensity values detected in WT samples while avoiding signal saturation. For a given experiment and tissue, imaging of all sections was completed in a single session, and identical imaging settings were used. Multi-field images were captured and stitched using the optimal path mode in Nikon NIS-Elements AR software (v5.30).
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3

Multichannel Microscopy Imaging Protocol

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Three stained sections from each sample were imaged at 10x magnification within 36 h of staining (except for sample C, which had unacceptable artefact in one section in Round 1). Whole‐section multichannel images were captured using a Nikon Ti2‐E motorised microscope with a Lumencor SOLA LED light engine (at 50% power), a Hamamatsu ORCA Fusion camera (in 16‐bit ultra‐quiet mode) and Nikon Plan Apochromat Lambda objectives. Final image resolution was 0.64 μm/pixel.
All exposures were chosen by the trained operators based on best microscopy practices of avoiding signal saturation while maximising the useful range of intensity values detected by the camera in healthy control samples. Identical imaging settings were used for all sections within the same round of staining and imaging. Operators selected exposures independently in Rounds 1 and 2, which approximates the degree of variation that is likely to arise between images collected in different laboratories using different microscopy equipment. For Round 3, the imaging operator was required to use the same exposure settings as those used in Round 1.
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