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We are at EBSA 2025 in Rome!

We are at EBSA 2025 in Rome!

We are at EBSA 2025 in Rome!

We’re thrilled to be attending the 14th European Biophysics Congress (EBSA 2025), taking place this week in Rome from June 30th to July 4th.

This major international event brings together the biophysics community to share cutting-edge research and foster collaboration. We’re proud to be part of it—showcasing our latest developments and connecting with researchers working at the frontier of molecular and cellular biophysics.

If you’re attending EBSA 2025, come find us! We’d love to meet you, show you our technology in action, and discuss how we can support your research with precision tools for force spectroscopy, cell mechanics, and beyond.

Join us to explore how our SENSOCELL technology enables calibration-free force measurements for applications in biophysics, mechanobiology, and single-molecule research. Whether you’re interested in cell membrane mechanics, intracellular microrheology, nucleus mechanotransduction, condensates LLPS, single-molecule or other biophysical applications, we’d love to discuss how our solutions can support your research!

Let’s connect in Rome!

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Fig. 1

Time dependence of trap position (top), force signal (middle) and Ca2+ fluorescence signal (bottom) recorded during a membrane tether pulling experiment. The force and Ca2+ ion channel activity signals exhibit negative correlation.

Fig. 2

Force and displacement data for two beads stimulated at frequencies of 4 Hz and 0.25 Hz. The progressive reduction of the beads displacement is in concomitancy with an increase of the applied force and loading rate.

Fig. 1

Schematic representation of the optical tweezers experiment. A fibronectin-coated bead is trapped, brought into contact with the cell membrane and stimulated with oscillations at different frequencies.

Fig.2

Time dependence of trap 1 and trap 2 position (top) and force (bottom) data along the different steps of the described dual tether pulling experiment.

Fig.1

Confocal video of the described dual tether pulling assay performed on a neuron axon. Courtesy of M. Krieg lab (ICFO).

Fig. 1

Time dependence of trap position (top), force signal (middle) and Ca2+ fluorescence signal (bottom) recorded during a membrane tether pulling experiment. The force and Ca2+ ion channel activity signals exhibit negative correlation.

Video 1

Confocal video showing a DVA neuron Ca2+ ion channel activity in a dynamic optical trapping assay. The pulling rate applied to the membrane tether is progressively increased. Scale bar = 5µm. Acquired at 10Hz.