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The sizes of fragments were measured by electron microscopy (microscope PREM-200, Moscow, USSR).
The cells' growth rating on Bürker cell and lipid accumulation revealed by Nile-red fluorescent dye (Sigma-Aldrich, N3013) was performed using optic and red fluorescence microscopy (microscope Zeis-Axioscop 2MOT), respectively.
Cell morphology was investigated with phase contrast microscopy (microscope Axiovert 35, Zeiss) and photographed with magnification 40× with a digital camera (Coolpix N25, Nikon).
Atomic force microscopy: Microscope glass coverslips were washed with detergent and water and then dried.
Slides were analysed by fluorescence microscopy (microscope model DMRXA; Leica Microsystems, Cambridge, UK).
Confocal image acquisition was performed on a Zeiss LSM780 laser scanning (Zeiss Microscopy) microscope.
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scanning probe microscopy and microscope.
scanning tunneling microscopy and microscope.
high-resolution transmission electron microscopy and microscope.
scanning transmission electron microscopy and microscope.
Morphology studies were carried out using a Jeol JSM-5600 Scanning Electron Microscopy (SEM) microscope (using the secondary electron mode).
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