Study on tissue culture and propagation of Maroco polo in vitro
Ruimei Liu
Abstract
Ruimei Liu
Abstract
The clone propagation of Maroco polo is developed through culture of scales and stems in vitro. Induction medium of shoots are MS+0.3~0.8 mg/L BA+0.05 mg/L NAA, MS+0.8 mg/L BA+0.1 mg/L NAA and MS+2 mg/L BA+0.05 mg/L NAA. Proliferation medium are MS+0.2 mg/L BA+0.1 mg/L NAA and MS+0.2 mg/L BA+0.1 mg/L IAA. Induction of roots are better in medium of 1/2 MS+0.2 mg/L KT+0.05~0.5 mg/L NAA active charcoal.
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The clone propagation of Maroco polo is developed through culture of scales and stems in vitro. Induction medium of shoots are MS+0.3~0.8 mg/L BA+0.05 mg/L NAA, MS+0.8 mg/L BA+0.1 mg/L NAA and MS+2 mg/L BA+0.05 mg/L NAA. Proliferation medium are MS+0.2 mg/L BA+0.1 mg/L NAA and MS+0.2 mg/L BA+0.1 mg/L IAA. Induction of roots are better in medium of 1/2 MS+0.2 mg/L KT+0.05~0.5 mg/L NAA active charcoal.
Key concepts: In vitro, Shoot, Tissue culture, Chemistry, Botany, Biology, Biochemistry