Abstract

An in vitro regeneration and molecular characterization of ginger protocols were established. Augmentation of MS-medium with 3 mg/l 2,4-D recorded the best results of callus production from young and primordial leaves of ginger. However, fortified of MS- with 1.0 mg/l BAP achieved of indirect shoots regeneration. The biochemical distinguish of regenerated plants with ginger original rhizomes was carried out using SDS-PAGE of protein and RAPD-PCR techniques. The biochemical markers showed highly similarity between them.

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