Simple tissue culture propagation technology for acerpalmatumseiryu
A technology of Acer japonica and Qinglong, which is applied in the field of plant tissue culture, can solve the problems such as that the tissue culture propagation method of Qinglong has not been reported, and achieves the effects of low production cost, simple culture process and easy operation.
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Embodiment 1
[0020] The simple tissue culture propagation process of Acer chinensis in chicken feet, which includes the following steps:
[0021] 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;
[0022] S2, inoculate the sterilized stem segment with buds on the medium for growth, such as figure 1 As shown, the medium is MS+NAA 0.3mg / L, and the inoculated culture material is placed in a culture room with an illumination intensity of 2000-3000LX, an illumination time of 16h / d, and a temperature of 24-26°C. , cultured for 15 days to induce axillary bud germination;
[0023] S3, rooting culture, cutting the directly induced axillary buds and inoculating on the rooting medium, such as figure 2 As shown, the rooting medium was 1 / 2MS+NAA0.3mg / L+IAA 0.2mg / L, and the...
Embodiment 2
[0025] The simple tissue culture propagation process of Acer chinensis in chicken feet, which includes the following steps:
[0026] 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;
[0027] S2, inoculate the sterilized stem segment with buds on the medium for growth, such as figure 1 As shown, the medium is MS+NAA 0.3mg / L, and the inoculated culture material is placed in a culture room with an illumination intensity of 2000-3000LX, an illumination time of 16h / d, and a temperature of 24-26°C. , cultured for 2 weeks to induce axillary bud germination;
[0028] S3, rooting culture, cutting the directly induced axillary buds and inoculating on the rooting medium, such as figure 2 As shown, the rooting medium was 1 / 2MS+NAA0.3mg / L+IAA...
Embodiment 3
[0030] The simple tissue culture propagation process of Acer chinensis in chicken feet, which includes the following steps:
[0031] 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;
[0032] S2, inoculate the sterilized stem segment with buds on the medium for growth, such as figure 1 As shown, the medium is MS+NAA 0.3mg / L, and the inoculated culture material is placed in a culture room with an illumination intensity of 2000-3000LX, an illumination time of 16h / d, and a temperature of 24-26°C. , cultured for 3 weeks to induce axillary bud germination;
[0033] S3, rooting culture, cutting the directly induced axillary buds and inoculating on the rooting medium, such as figure 2 As shown, the rooting medium was 1 / 2MS+NAA0.3mg...
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