Rooting induction method for tissue-cultured seedlings of Lithocarpus hancei (Benth.) Rehd
A technique for tissue cultured seedlings and Keke keel, applied in the field of induction of rooting of kebab tissue cultured seedlings, can solve problems such as uneven rooting, not thick root system, and small number of roots, so as to achieve more roots, shorten the rooting cycle, and develop roots fast effect
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Embodiment 1
[0022] Select the subcultured buds of Coryne sylvestris that have been cultured for 35-36 days in the conventional tissue culture. After the surface of the bottle is sterilized, in the aseptic space on the ultra-clean workbench, select the single bud cluster that grows robustly and has a height of 1-2 cm. For buds, cut at 2-3mm below the node, and remove the base leaves and petioles. The pruned single buds were inoculated in the pre-rooting medium, and placed under the conditions of temperature 20±1°C, humidity 40%, light intensity 2000lux, and light 16h / d for pre-rooting culture. The raw material content of the pre-rooting medium described therein is: 1 / 2 improved MS medium+NAA 1.0mg / L+vitamin C6g / L++VC 15mg / L+glucose 25g / L+agar 5.0g / L.
[0023] After 30-35 days of pre-rooting culture for single buds, transfer the single buds to the rooting medium and place them under the conditions of temperature 20±1°C, humidity 40%, light intensity 2000lux, and light 16h / d for rooting cult...
Embodiment 2
[0026] Select the subcultured buds of Keke keel that have been cultured for 36-37 days in conventional tissue culture. After disinfecting the surface of the bottle, in the aseptic space on the ultra-clean workbench, select a single bud cluster that grows robustly and has a height of 1-2 cm. For buds, cut at 2-3mm below the node, and remove the base leaves and petioles. The pruned single buds were inoculated in the pre-rooting medium, and placed under the conditions of temperature 20±1°C, humidity 40%, light intensity 2500lux, and light 15h / d for pre-rooting culture. The raw material content of the pre-rooting medium described therein is: 1 / 2 improved MS medium+NAA 1.5mg / L+vitamin C6g / L++VC 15mg / L+glucose 25g / L+agar 5.0g / L.
[0027] After 30-35 days of pre-rooting culture for single buds, transfer the single buds to the rooting medium and place them under the conditions of temperature 20±1°C, humidity 40%, light intensity 2500lux, and light 15h / d for rooting culture. The raw m...
Embodiment 3
[0030] Select the subcultured buds of Coryne sylvestris that have been cultured for 37-38 days in the conventional tissue culture, and after the surface of the bottle is disinfected, in the aseptic space on the ultra-clean workbench, select a single bud cluster that grows robustly and has a height of 1-2 cm. For buds, cut at 2-3mm below the node, and remove the base leaves and petioles. The pruned single buds were inoculated in the pre-rooting medium, and placed under the conditions of temperature 20±1°C, humidity 45%, light intensity 2000lux, and light 16h / d for pre-rooting culture. The raw material content of the pre-rooting medium described therein is: 1 / 2 improved MS medium+NAA 2.0mg / L+vitamin C6g / L++VC 15mg / L+glucose 25g / L+agar 5.0g / L.
[0031] After 30-35 days of pre-rooting culture for single buds, transfer the single buds into the rooting medium, and place them under the conditions of temperature 20±1°C, humidity 45%, light intensity 2000lux, and light 16h / d for rootin...
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