"The Dhyana 400BSI V3 runs at the speed and sensitivity we need for lightsheet microscopy, and we have built our own control software using the Tucsen SDK."

- Ludovico Silvestri, Silvestri Group,
European Laboratory for Non-linear Spectroscopy (LENS), University of Florence

1 of 4

Group Research Aims

The Silvestri group develops advanced light-sheet fluorescence microscopy (LSFM) methods to uncover how brain circuits encode behaviour. Their research integrates tissue clearing, high-resolution optical imaging, and computational analysis to achieve whole-brain mapping at cellular resolution. By creating scalable tools such as BRANT, they quantify neuronal activation patterns during learning, memory, and emotional processing. Functional analysis is paired to anatomical mapping of single axons by imaging expanded samples. The group’s goal is to link microscopic neural activity with macroscopic brain function, revealing how distributed networks change across states and between sexes. Through continuous innovation in imaging and data analysis, the lab strives to push the boundaries of systems neuroscience and brain-wide mapping.

Silvestri group lightsheet data 3D histology

Experiments & Equipment

The Silvestri group develops advanced light-sheet microscopy methods to uncover how brain circuits encode behaviour. Their research integrates tissue clearing, high-resolution optical imaging, and computational analysis to achieve whole-brain mapping at cellular resolution. By creating scalable tools such as BRANT, they quantify neuronal activation patterns during learning, memory, and emotional processing. The group’s goal is to link microscopic neural activity with macroscopic brain function, revealing how distributed networks change across states and between sexes. Through continuous innovation in imaging and data analysis, the lab strives to push the boundaries of systems neuroscience and brain-wide mapping.

Their current work uses light-sheet fluorescence microscopy (LSFM) to capture 3D structural imaging of intact murine cells, enabling volumetric visualization across cleared tissue blocks. With custom hardware and software, they can accelerate frame rates and reduce photobleaching, combining it with tissue clearing, fluorescence labelling, and image segmentation to reconstruct cellular morphology in situ. The experiments validate LSFM as a tool for 3D imaging of muscle injury and repair, requiring fast imaging, with good resolution for structural mapping of large, complex tissue samples.

Experience with Tucsen

"The development of our research was previously limited by the time needed to collect data from large tissue sections. Working with Tucsen was straightforward: we demoed several cameras, selected the best for field of view and speed, received a same-day quote, and the camera was delivered on time and even installed on-site. The highly sensitive and fast readout of the Dhyana 400BSI V3 enables quicker data collection without sacrificing signal level, and line time delay mode enables straightforward integration into our system."

- Ludovico Silvestri, LENS, University of Florence

Tucsen Dhyana 400BSI V3

Dhyana 400BSI V3

The Dhyana 400BSI V3 uses the GSENSE2020BSI sensor which gives high sensitivity sCMOS capabilities as well as rolling shutter control mode to synchronise scanning for lightsheet microscopy.

  • 95% QE
  • Up to 100 fps
  • 1e- Read Noise
  • 4 Million Pixels
  • 6.5 Micro Pixels
  • CameraLink & USB3.0