Cryptomeria fortunei clone in-vitro rooting culture method
A technology for rooting culture and clones, applied in the field of plant rooting culture, can solve problems such as low seed germination rate, and achieve the effect of meeting the needs of industrial use and good practicability
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Embodiment 1
[0024] 1) Sterilization and bottle fixing of sprouts
[0025] Cut out the young and young shoots of the fine cedar cedar clone 011#, remove the excess leaves, soak in detergent diluted with deionized water for 30 minutes, and then rinse with running water for 1 hour. Under sterile conditions, soak in 70% alcohol for 90s, then treat with 0.1% mercuric chloride for 10 minutes, and then rinse with sterile water for 3-4 times, each time for 1-2 minutes. During the sterilization process of the medicinal solution, gently shake the triangular flask so that the sterilization solution fully contacts the explants. After rinsing, place it in a petri dish, and after the sterile filter paper absorbs the residual water, cut off the injured parts at both ends of the stem to reduce the poison of mercury liter. Then it was cut into 2-3cm long stem segments, inoculated on sterilized MS medium, and cultured for 2 weeks.
[0026] 2) Differentiation and elongation of buds
[0027] Put the tissu...
Embodiment 2
[0046] 1) Sterilization and bottle fixing of sprouts
[0047] Cut off young and young shoots of the fine cedar cedar clone 3# in the same year, remove excess leaves, soak in detergent diluted with deionized water for 30 minutes, and then rinse with running water for 1 hour. Under sterile conditions, soak in 70% alcohol for 90s, then treat with 0.1% mercuric chloride for 10 minutes, and then rinse with sterile water for 3-4 times, each time for 1-2 minutes. During the sterilization process of the medicinal solution, gently shake the triangular flask so that the sterilization solution fully contacts the explants. After rinsing, place it in a petri dish, and after the sterile filter paper absorbs the residual water, cut off the injured parts at both ends of the stem to reduce the poison of mercury liter. Then it was cut into 2-3cm long stem segments, inoculated on sterilized MS medium, and cultured for 2 weeks.
[0048] 2) Differentiation and elongation of buds
[0049] Put th...
Embodiment 3
[0066] 1) Sterilization and bottle fixing of sprouts
[0067] Cut out young and young shoots of the fine cedar cedar clone 70#, remove excess leaves, soak in detergent diluted with deionized water for 30 minutes, and then rinse with running water for 1 hour. Under sterile conditions, soak in 70% alcohol for 90s, then treat with 0.1% mercuric chloride for 10 minutes, and then rinse with sterile water for 3-4 times, each time for 1-2 minutes. During the sterilization process of the medicinal solution, gently shake the triangular flask so that the sterilization solution fully contacts the explants. After rinsing, place it in a petri dish, and after the sterile filter paper absorbs the residual water, cut off the injured parts at both ends of the stem to reduce the poison of mercury liter. Then it was cut into 2-3cm long stem segments, inoculated on sterilized MS medium, and cultured for 2 weeks.
[0068] 2) Differentiation and elongation of buds
[0069] Put the tissue materia...
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