Abstract
The present study established cell suspensions from the friable callus derived from the stem explant of broad bean (Vi cia faba) axenic seedlings. These suspensions of certain densities were cultured by embedding in agar, using three methods of culture including, multiple drop arrays (MDA), thin layers and sectors. In the presence of MS and
SH liquid medium forming solid - liquid medium. The results indicated that all methods succeeded at culturing cell
suspension using MS medium. Moreover, these methods sustained callus f01mation. Multiple Drop Array (MDA) induced callus at ratio of 68% in MS medium, and 48% in SH medium. All pieces of callus primordia
continued their growth and increased in size.