Subject |
Biophysics |
Specific subject area |
Optical Brillouin and Raman spectroscopy |
Type of data |
Raw and graph. The raw data are available in "Appendix A. Supplementary data" of the present article as zip file. |
How data were acquired |
Custom build microscope coupled with Brillouin and Raman spectrometers [6,7] |
Data format |
Raw |
Parameters for data collection |
The laser beam with λ = 532 nm and power on the sample P<3.5 mW is focalized on the single cells using UPLSAPO 60XW Olympus objective with NA1.2. In order to control the position on the cell, the Petri dish, thermalized at 37 °C, was inserted in a dedicated sample environment placed on a xyz translator stage (PI 611-3S Nanocube XYZ). Thanks to the piezoelectric control, it reaches a spatial resolution of 10 nm in a motion range of 100 μm for each axis. |
Description of data collection |
The Raman spectra were acquired by RM- Horiba iHR320 Triax using a 600 grooves mm−1 grating and an N2 cooled CCD detector (1024 × 256 pixels). The acquisition of Raman spectra up to 3000 cm−1 frequency shift is possible in this condition. At the same time, the High Contrast HC version of the Sandercock type tandem Fabry Perot (TFP-2) interferometer was used to acquire Brillouin spectra. |
Data source location |
IOM-CNR c/o Department of Physics and Geology University of Perugia Italy |
Data accessibility |
With the article |