Tissue culture method for heuchera micrantha 'Palace Purple'
A technique of tissue culture and coral clocks, applied in horticultural methods, botany equipment and methods, horticulture, etc., can solve the problems of small number of introduced species and slow propagation of ramets, etc., to maintain the traits of the female parent, improve the reproduction speed and the growth of seedlings The effect of uniformity
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Embodiment 1
[0027] (1) Obtaining sterile materials
[0028] Take the germinated young shoots, 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, use sterile filter paper to blot the water on the surface of the buds, cut the buds into 0.5cm-long segments with axillary buds, and inoculate them with MS+6-BA1.0mg / L+NAA0.1mg / L bud induction medium;
[0029] (2) Differentiation and proliferation of buds
[0030] One week after the segments were inoculated on the axillary bud induction medium, the axillary buds began to expand and green protrusions appeared, and after 3 weeks, bud meristems could be seen. After culturing for another month, the small buds formed clusters, and the adventitious buds were cut off and transferred to the MS+6-BA0.5mg / L+NAA0.05mg / L ...
Embodiment 2
[0039] (1) Obtaining sterile materials
[0040] Take the germinated young shoots, remove the wrapped 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 of the buds, cut the buds into 1cm-long segments with axillary buds, and inoculate them in a medium containing MS+6-BA2.0mg / L+NAA0.2mg / On the shoot induction medium of L;
[0041] (2) Differentiation and proliferation of buds
[0042] 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 3 weeks, bud meristems could be seen. After culturing for another month, the small buds formed clusters. Cut off the adventitious buds and transfer them to MS+6-BA2.0mg...
Embodiment 3
[0051] (1) Obtaining sterile materials
[0052] Take the germinated young shoots, remove the wrapped 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 of the buds, cut the buds into 2cm-long segments with axillary buds, and inoculate them in a medium containing MS+6-BA3.0mg / L+NAA0.3mg / On the shoot induction medium of L;
[0053] (2) Differentiation and proliferation of buds
[0054]After the segments were inoculated on the axillary bud induction medium for 3 weeks, the axillary buds began to expand and green protrusions appeared, and after 5 weeks, bud meristems could be seen. After 2 months of culture, the small buds formed clusters, and the adventitious buds were cut off and transferred to the MS+6-B...
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