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Experience the power of fast and gentle volumetric imaging.

Obtain more physiologically relevant data.

DLS and STELLARIS enable even gentler imaging giving you the ability to perform fast and gentle volumetric light sheet imaging and to improve your live cell imaging applications by increasing cell viability thanks to:

  • single plane illumination
  • fast imaging with a sensitive sCMOS camera
  • significantly increased spectral possibilities and the ability to perform even gentler imaging using excitation wavelengths in the far-red spectrum
  • capacity to generate a light sheet with the resonant scanner which results in shorter pixel dwell times and, consequently, less phototoxic effects.
  • obtain light sheet results with improved contrast and signal-to-noise ratio thanks to the LIGHTNING information extraction solution for DLS data.
Light sheet experiments of organoids or spheroids with DLS allow you to image >100 μm in depth. Live mammary epithelial spheroid: green nuclei, (MCF10A H2B-GFP); red tubulin cytoskeleton (SiR-tubulin); DLS data processed with LIGTHNING. Courtesy of B. Eismann and C. Conrad, at BioQuant/DKFZ Heidelberg, Germany.
Light sheet experiments of organoids or spheroids with DLS allow you to image >100 μm in depth. Live mammary epithelial spheroid: green nuclei, (MCF10A H2B-GFP); red tubulin cytoskeleton (SiR-tubulin); DLS data processed with LIGTHNING. Courtesy of B. Eismann and C. Conrad, at BioQuant/DKFZ Heidelberg, Germany.

Light sheet with confocal benefits

Thanks to the seamless integration of DLS, your light sheet imaging benefits from the technical innovations of your STELLARIS system.

Always the right laser

All visible lasers of your STELLARIS confocal are ready to be used for light sheet imaging. There is much flexibility when choosing the right dye for your light sheet experiments with the optional diode laser lines as well as the STELLARIS next generation White Light Lasers. You can now even unlock the imaging of near-infrared dyes.

Always the right scanner

On STELLARIS systems equipped with a tandem scanner, you can choose between the resonant scanner or the field-of-view scanner (at 1400Hz) to generate the scanned light sheet. Generating the light sheet with the resonant scanner produces shorter pixel dwell times, which enables even more gentle imaging.

STELLARIS 8 & STELLARIS 5 laser configurations
STELLARIS 8 & STELLARIS 5 laser configurations

Enhance the potential of your research with a system that adapts to your needs

Experience the flexibility to image different types of samples.

  • Image living samples and cleared specimens, such as organoids, tissue, or whole-developing organisms, in the same system and without difficult hardware changes
  • Easy exchange of a growing number of detection objectives and TwinFlect mirrors to shape the light sheet depending on your needs
  • DLS objectives cover water-based to organic clearing reagents
State-of-the-art tissue-clearing methods provide subcellular-level optical access to intact tissues from individual organs. This image shows a cleared mouse kidney sample acquired using the 16x multi-immersion objective. Illumination was performed using 730 nm. Courtesy of Prof Gretz, University of Mannheim, Germany.
State-of-the-art tissue-clearing methods provide subcellular-level optical access to intact tissues from individual organs. This image shows a cleared mouse kidney sample acquired using the 16x multi-immersion objective. Illumination was performed using 730 nm. Courtesy of Prof Gretz, University of Mannheim, Germany.

Manipulate your specimen using confocal technology

Our light sheet module is more than a functional add-on to your confocal. STELLARIS and DLS synergize to expand the options for your research. For example, you can manipulate your specimens using the confocal technology and then image with DLS.

It is simply done by switching between confocal and light sheet mode in the LAS X software. This way, photoconversion or wounding experiments with subsequent gentle long-term observations become easy and convenient.

Straightforward sample manipulation

  • Easy access to your specimen to perform drug treatments
  • Ability to manipulate your specimens using the confocal technology for photoconversion and wounding experiments followed by gentle and fast DLS imaging
This example demonstrates the advantage of confocal combined with DLS. A transgenic Zebrafish embryo was labelled to visualize macrophages involved in immune responses. To investigate their behavior upon wounding, a confocal laser was used to create a wound (arrow) and afterwards, a time-lapse movie was recorded. The video shows the dynamic reaction of the activated cells that are now migrating to the wound triggering the healing process. For this case, switching to DLS allows gentle live-cell imaging of the Zebrafish.

Increase productivity of your light sheet experiments

Keep your workflow and sample handling.

  • Easy incorporation of your specimens into your light sheet experimental workflow thanks to DLS unique Twinflect design.
  • Transition between confocal and light sheet experiments without the need of additional cumbersome experimental setups.
  • Keep the sample preparation you are familiar with
  • mount and image several samples with multi-positioning experiments.
  • Perform a tile scan of very large samples by using DLS in combination with the confocal system stage automation.
  • Switch easily between fluorescence and widefield imaging for convenient sample navigation.
  • Provide cellular and organismal context for fluorescence optical sections by using the widefield mode for acquisitions.
High-resolution imaging of large whole specimens: The tile scan option allows complete imaging of large specimens, like the whole zebrafish embryo shown here, at high resolution. Courtesy of Elvire Guiot, IGBMC Imaging Center, Illkirch-Graffenstaden, France and Julien Vermot, Imperial College London, United Kingdom.
High-resolution imaging of large whole specimens: The tile scan option allows complete imaging of large specimens, like the whole zebrafish embryo shown here, at high resolution. Courtesy of Elvire Guiot, IGBMC Imaging Center, Illkirch-Graffenstaden, France and Julien Vermot, Imperial College London, United Kingdom.

Workflow-oriented software design

The LAS X software guides users step by step through data recording and evaluation. The workflow-oriented design helps you to use the instrument more efficiently. A convenient calibration routine establishes the light sheet precisely.

Dual-sided illumination of the sample comes by design: each of the two opposing mirrors of the TwinFlect can be targeted by the scanner to overcome darker areas. For crisp images with a large field of view, you can merge the two images using the online or offline fusion option of the LightSheet Wizard in the LAS X software.

Tailor LAS X to your needs with additional software packages. The LAS X 3D Visualization module provides novel ways to interact with your 3D data by intuitive clipping, fast rendering, and stereo display. Tile scanning experiments enable you to observe large areas. Mark & Find experiments allow you to observe several regions of interest in a multi-position set up.

Workflow-oriented software design of LAS X microscope software
Workflow-oriented software design of LAS X microscope software

Conduct and document long-term observations

Imaging requires light, but too much light can damage your cells. Light sheet microscopy is the most gentle imaging method to date, as it reduces the overall photodamage from phototoxicity and bleaching. This automatically increases the viability of your specimen.

Particularly developmental biology benefits from light sheet imaging. The combination of low light illumination and high-speed acquisition allows you to follow sensitive, developing organisms like a Drosophila embryo over long periods of time and to understand how tissue and organs form in real time and 3D.

Low phototoxicity and specimen imaging in 3D: Development of Drosophila melanogaster over 6 hours. Probe: Light-sensitive RFP. 3D rendering. 150 µm z stack, 30 sec/stack.
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