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- 采用MSR3c (MS +casaminoacids 5 0 0mg/L +glutamine 30 0mg/L +proline 5 0 0mg/L +mannitol 36 4 g/L +maltose 30 g/L +TDZ 0 2mg/L +phytagel 5 g/LpH5 8)為分化培養基 ,愈傷組織分化率均在 90%以上。The shoots differentiation rate of the callus cultured in differentiation medium (MSR 3c,MS +casamino acids 500 mg/L +glutamine 300 mg/L +proline 500 mg/L +mannitol 36.4 g/L+maltose 30 g/L+TDZ 0.2 mg/L +phytagel 5 g/L pH 5.8) was over 90%25.
