Abstract
Meristems aseptically isolated from shoots developed on sugarbeet (Beta vulgaris L.) inflorescences were precultured on modified MS agar medium containing 19.4 μM 6-benzylaminopurine, 6 μM triiodobenzoic acid, and supplemented with 5% DMSO. After two days the meristems were transferred to liquid modified MS medium and the cryoprotectants sorbitol and DMSO added in varying concentrations. The meristems were frozen to −40°C and stored in liquid nitrogen. Growth resumed when the meristems were quick-thawed at 39°C.
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Braun, A. Cryopreservation of sugarbeet germplasm. Plant Cell Tiss Organ Cult 14, 161–168 (1988). https://doi.org/10.1007/BF00043406
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DOI: https://doi.org/10.1007/BF00043406