In vitro axillary shoot proliferation was achieved from single-node explants of Indigofera tinctoria on a welldefined medium, Murashige and Skoog (MS) medium supplemented with 1.0 mg l −1 N 6 -benzyl adenine (BA) and 0.1 mg l −1 indole-3-acetic acid. Axillary shoot meristems from cultures derived from up to three subcultures were used in the encapsulation-dehydration technique. Preconditioned, calcium alginate-encapsulated, and precultured axillary shoot meristems were subjected to different lengths of desiccation in a laminar flow cabinet. Maximum survival and regeneration rates of 56.7% and 62.2%, respectively, were obtained in half-strength (half the macro-and micronutrients and full-strength vitamins) MS medium supplemented with 0.5 mg l −1 gibberellic acid and 0.2 mg l −1 BA after 4 h of desiccation, during which the moisture content was reduced to 16.0%. According to the analysis of six random amplified polymorphic DNA markers, plantlets derived from cultures initiated with cryopreserved plant material were genetically identical to those derived from nonfrozen (control) tissues.