“…Tissues were rinsed three times in phosphate buffer (4 °C) and dehydrated (5, 10, 15, 20, 25, 30, 40, 50, 60, 70, 80, and 90% ethanol solution, pure ethanol, ethanol and propylene oxide solution [1:1], pure propylene oxide). Next, material was embedded in epon resin, which was polymerised in 35 °C, 45 °C and 60 °C (for 24 h at each temperature), cut with Tesla ultramicrotome (semi-thin transverse sections were obtained), stained with PAS (Periodic Acid, Schiff) and toluidine blue, and mounted in Euparal (Karczewska et al 2009;Miczajka et al 2014;Miodek et al 2022). Sections were examined under Olympus BX41 microscope (bright field).…”