Dempsey G P, Bullivant S
J Microsc. 1976 Apr;106(3):261-71. doi: 10.1111/j.1365-2818.1976.tb02406.x.
Two methods are described for fracturing unfixed, uncryoprotected mouse liver that had been frozen by contact with a copper block at liquid nitrogen temperature. The best method involved precise fracturing of a few microns of surface tissue with a cooled glass knife, using the Cryokit attachment of the LKB III ultramicrotome. The resulting replicas were free from electron microscopically-visible ice crystals. A noticeable feature of replicas from unfixed, uncryoprotected tissue was the extent of plastic deformation of certain cellular structures. Cytoplasmic macromolecules, and to a lesser extent intramembranous particles, often appeared to be 'stretched' to form fibrils.