Tissue culture method of floral leaf pampasgrass
A technology of tissue culture and pampas grass, which is applied in the field of tissue culture of pampas grass, which can solve the problems of limited supply of seedlings, small number of introduced pampas grass, etc., to improve stability, increase speed of reproduction and neatness of seedlings degree of effect
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Embodiment 1
[0028] (1) Obtaining sterile materials
[0029] Take the young buds that have germinated in spring, remove the wrapped leaves, wash them with tap water for 1 hour, put them on the ultra-clean workbench, soak them in ethanol with a mass concentration of 70% for 10 seconds, and then soak them in mercury with a volume concentration of 0.5‰ for 10 minutes. Rinse 4 times with sterile water again, use sterile filter paper to blot the moisture on the surface, then cut into 0.5cm-long segments with axillary buds, and inoculate the segments with MS+6-BA1.0mg / L+NAA0. On the axillary bud induction medium of 1mg / L;
[0030] (2) Differentiation and proliferation of buds
[0031] After the segments were inoculated on the axillary bud induction medium for 1 week, the axillary buds began to expand and green protrusions appeared. After 3 weeks, bud meristems could be seen. After culturing for 1 month, the small adventitious buds could grow to 3 cm. Cut the adventitious buds Under transfer in...
Embodiment 2
[0040] (1) Obtaining sterile materials
[0041] Take the young buds that have germinated in spring, remove the wrapped leaves, wash them with tap water for 2 hours, put them on an ultra-clean workbench, and soak them in ethanol with a mass concentration of 75% for 30 seconds, and mercury with a volume concentration of 1‰ for 15 minutes. Rinse 5 times with sterile water, use sterile filter paper to blot the water on the surface, then cut into 1cm-long segments with axillary buds, and inoculate the segments with MS+6-BA2.0mg / L+NAA0.2mg / L on the axillary bud induction medium;
[0042] (2) Differentiation and proliferation of buds
[0043] After the segments were inoculated on the axillary bud induction medium for 2 weeks, the axillary buds began to expand and green protrusions appeared. After 4 weeks, bud meristems could be seen. After culturing for 1 month, the small adventitious buds could grow to 4cm. Cut the adventitious buds Under transfer into the adventitious bud prolif...
Embodiment 3
[0052] (1) Obtaining sterile materials
[0053] Take the young buds that have germinated in spring, remove the leaves wrapped outside, rinse them with tap water for 3 hours, put them on the ultra-clean workbench, and soak them in ethanol with a mass concentration of 75% for 50 seconds, and mercury with a volume concentration of 2‰ for 30 minutes. Rinse 6 times with sterile water, use sterile filter paper to blot the water on the surface, then cut into 2cm-long segments with axillary buds, and inoculate the segments with MS+6-BA5.0mg / L+NAA0.5mg / L on the axillary bud induction medium;
[0054] (2) Differentiation and proliferation of buds
[0055] After the segments were inoculated on the axillary bud induction medium for 3 weeks, the axillary buds began to expand and green protrusions appeared. After 5 weeks, bud meristems could be seen. After 2 months of culture, the small adventitious buds could grow to 4cm. Cut the adventitious buds Under transfer into the adventitious bud ...
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