Abstract
A method for rapid and highly effective plant micropropagation from vegetative meristems was established for Aloe barbadensis Mill. Plant micropropagation was achieved culturing apices on medium containing 1.1 μM 2,4-dichlorophenoxyacetic acid and 2.3 μM kinetin for 15–30 days. High morphogenetic ability was maintained by transferring explants (after 60 days) on media containing 0.11 μM 2,4-dichlorophenoxyacetic acid and 2.2 μM 6-benzylaminopurine.
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