Embryogenic suspension cells from Litchi (Litchi chinesis Sonn ) was vitrified and then cryopreserved. Three days old embryogenic suspension cells were precultured for 2 days at 25% on MS medium supplemented with 0.4mol/L glucitol, and then loaded in a vitrification solution containing 60% PVS2 for 15 minutes at room temperature. The embryogenic suspension ceils were sufficiently dehydrated with vitrification solution containing 100% PVS2 for 15-20 minutes at 0℃. After the solution was changed with fresh PVS2, the suspensions were immersed i...