2004GuihaiaRequires access

Study on tissue culture and propagation of Maroco polo in vitro

Ruimei Liu

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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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What this paper is about

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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Available 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.

Key concepts: In vitro, Shoot, Tissue culture, Chemistry, Botany, Biology, Biochemistry

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