Tissue culture method for tulbaghia violacea
A technology of tissue culture and Zijiaohua, which is applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of slow planting of ramets or bulbs, limited seedlings, and a small number of Zijiaohua introductions, and achieves improvement. Propagation speed and uniformity of seedlings, and the effect of improving stability
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Embodiment 1
[0028] (1) Obtaining sterile materials
[0029] Take the germinated young buds and flower buds in spring, remove the leaves, wash them with tap water for 1 hour, put them on an 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, use sterile filter paper to blot the water on the surface, then cut into 0.5cm-long segments and buds with axillary buds, and inoculate the segments and buds in a medium containing MS+6-BA2.0mg / On the bud induction medium of L+NAA0.2mg / L;
[0030] (2) Differentiation and proliferation of buds
[0031] After the segments and buds were inoculated on the bud induction medium for 2 weeks, the axillary buds began to expand, and yellow-green protrusions appeared. After 4 weeks, bud meristems could be seen. After culturing for 1 month, small adventitious buds could grow to 2 cm. Cut off the adventitiou...
Embodiment 2
[0040] (1) Obtaining sterile materials
[0041] Take the germinated young buds and flower buds in spring, remove the leaves, wash them with tap water for 2 hours, put them on the ultra-clean workbench, soak them in ethanol with a mass concentration of 75% for 30 seconds, and then soak them in 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 and buds with axillary buds, and inoculate the segments and buds in a medium containing MS+6-BA5.0mg / L +NAA0.5mg / L bud induction medium;
[0042] (2) Differentiation and proliferation of buds
[0043] After the segments and buds were inoculated on the bud induction medium for 3 weeks, the axillary buds began to swell, and yellow-green protrusions appeared. After 5 weeks, bud meristems could be seen. After 2 months of further cultivation, small adventitious buds could grow to 3 cm. The adventitious buds were...
Embodiment 3
[0052] (1) Obtaining sterile materials
[0053] Take the germinated young buds and flower buds in spring, remove the leaves, wash them with tap water for 3 hours, put them on the ultra-clean workbench, soak them in ethanol with a mass concentration of 75% for 50 seconds, and then soak them in 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 and buds with axillary buds, and inoculate the segments and buds with MS+6-BA5.0mg / L +NAA0.5mg / L bud induction medium;
[0054](2) Differentiation and proliferation of buds
[0055] After the segments and buds were inoculated on the bud induction medium for 4 weeks, the axillary buds began to expand, and yellow-green protrusions appeared. After 6 weeks, bud meristems could be seen. After 2 months of cultivation, small adventitious buds could grow to 3 cm. The adventitious buds were cut and transferred to th...
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