Acer palmatum Seiryu tissue culture propagation process
A technology of Acer palmatum and Qinglong, which is applied in the field of plant tissue culture, can solve the problems that Qinglong tissue culture propagation methods have not been reported, and achieve the effects of low production cost, short reproduction cycle and simple formula
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Embodiment 1
[0022] The tissue culture propagation process of Acer chinensis in chicken feet, it includes the following steps:
[0023] S1. Collect disease-free stems of the same year at noon or afternoon on a sunny day, remove excess leaves, and cut them into stems with buds. Sterilize the stems with alcohol for 30s, then sterilize with mercury chloride for 5 minutes, and then Wash 4-6 times with sterile water;
[0024] S2, inoculate the stem segment with buds after sterilization on a medium for growth, the medium is MS+NAA 0.3mg / L, and the inoculated culture material is placed in a light intensity of 2000~3000LX, and the light time is 16h / d, the temperature is 24 ~ 26 ℃ culture room, culture for 15 days, inducing the germination of axillary buds, such as figure 1 shown;
[0025] S3, subculture proliferation culture, cut off the germinated axillary buds, inoculate on the subculture medium, the subculture medium is MS+6-BA 1.5mg / L +NAA 0.3mg / L, and the inoculated culture The material is...
Embodiment 2
[0028] The tissue culture propagation process of Acer chinensis in chicken feet, it includes the following steps:
[0029] S1. Collect disease-free stems of the same year at noon or afternoon on a sunny day, remove excess leaves, and cut them into stems with buds. The stems with buds are first sterilized with alcohol for 50s, then sterilized with mercury chloride for 4min, and then Wash 4-6 times with sterile water;
[0030] S2, inoculate the stem segment with buds after sterilization on a medium for growth, the medium is MS+NAA 0.3mg / L, and the inoculated culture material is placed in a light intensity of 2000~3000LX, and the light time is 16h / d, the temperature is 24 ~ 26 ℃ culture room, culture for 2 weeks, inducing the germination of axillary buds, such as figure 1 shown;
[0031] S3, subculture proliferation culture, cut off the germinated axillary buds, inoculate on the subculture medium, the subculture medium is MS+6-BA 1.5mg / L +NAA 0.3mg / L, and the inoculated culture...
Embodiment 3
[0034] The tissue culture propagation process of Acer chinensis in chicken feet, it includes the following steps:
[0035] S1. Collect disease-free stems of the same year at noon or afternoon on a sunny day, remove excess leaves, and cut them into stems with buds. The stems with buds are first sterilized with alcohol for 60s, then sterilized with mercuric chloride for 3 minutes, and then Wash 4-6 times with sterile water;
[0036] S2, inoculate the stem segment with buds after sterilization on a medium for growth, the medium is MS+NAA 0.3mg / L, and the inoculated culture material is placed in a light intensity of 2000~3000LX, and the light time is 16h / d, the temperature is 24 ~ 26 ℃ culture room, culture for 3 weeks, inducing the germination of axillary buds, such as figure 1 shown;
[0037] S3, subculture proliferation culture, cut off the germinated axillary buds, inoculate on the subculture medium, the subculture medium is MS+6-BA 1.5mg / L +NAA 0.3mg / L, and the inoculated c...
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