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

M 2,4-dichlorophenoxyacetic acid and 2.3

M kinetin for 15–30 days. High morphogenetic ability was maintained by transferring explants (after 60 days) on media containing 0.11

M 2,4-dichlorophenoxyacetic acid and 2.2

M 6-benzylaminopurine.
Key words
Aloe barbadensis
- in vitro plant micropropagation - morphogenetic ability