Artificial quick propagation method for hemsley rockvine root
A gold-threaded gourd and artificial technology, applied in horticultural methods, botany equipment and methods, gardening tools/equipment, etc., can solve the problems of artificial rapid propagation of golden-wired gourds that have not yet been seen, and resources cannot meet the needs of clinical treatment, etc. , to achieve the effect of saving rare and endangered plants, low cost, and developed root system
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Embodiment 1
[0050] 1) Pretreatment of explants: cutting rattans with a length of 10-15 cm, rinsing with tap water with 1% detergent by volume, and then rinsing with tap water for about 30 minutes.
[0051] 2) Sterilization of explants: sterilize the pretreated materials on an ultra-clean workbench, soak them in alcohol with a volume ratio of 75% for 0.5-1.0 min, rinse them once with sterile water, and then Sterilize with 0.1% mercuric chloride solution by weight for 10-15 minutes, or sterilize with 2% sodium hypochlorite aqueous solution for 10-15 minutes by volume, and finally rinse with sterile water for 3-5 times.
[0052] 3) Inoculation: put the sterilized material on the sterilized filter paper to blot dry, cut out terminal buds and stem segments with axillary buds about 0.5-1.0 cm long with a scalpel, and inoculate them in the induction medium.
[0053] 4) Induction culture: Induction culture until terminal buds and axillary buds are induced, callus occurs at the base of the stem se...
Embodiment 2
[0068] 1) Explant pretreatment: cut rattans with a length of 10-15 cm, rinse with tap water with 1% detergent, and rinse with tap water for about 30 minutes.
[0069] 2) Sterilization of explants: sterilize the pretreated materials on an ultra-clean workbench, first soak in 75% alcohol for 0.5-1.0min, rinse once with sterile water, and then use 0.1% Sterilize with mercuric chloride solution for 10 to 15 minutes, or with 2% sodium hypochlorite aqueous solution for 10 to 15 minutes, and finally rinse with sterile water for 3 to 5 times.
[0070] 3) Inoculation: put the sterilized material on the sterilized filter paper to blot dry, cut out terminal buds and stem segments with axillary buds about 0.5-1.0 cm long with a scalpel, and inoculate them in the induction medium.
[0071] 4) Induction culture: Inoculate the terminal buds and stem segments with axillary buds in the bud induction medium of MS+6-BA 2mg / L+IBA0.2mg / L+sugar 30g / L+agar 7g / L. After 10 days of induction culture, ...
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