The Method of Rapid Breeding by Utilizing Pinellia Stems
A kind of Pinellia, fast technology, applied in the field of traditional Chinese medicine, can solve problems such as unfavorable large-scale production, and achieve the effects of favorable air circulation, fast breeding speed and short cultivation period
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Embodiment 1
[0047] Embodiment 1 adopts the method of the present invention to carry out breeding
[0048] Disinfection and sterilization of the culture container: use a plant tissue culture box that can be autoclaved (the material is polypropylene, the culture box is a 25×25cm square box, and the box cover has 1 to 3 openable air holes). The body and the lid form a box with an overall height of 4.5cm, which is autoclaved for use.
[0049] Medium preparation: The medium used in the present invention is a liquid MS induction medium without any auxin, see Table 1.
[0050] Inoculation: Select and cultivate strong virus-free seedlings with a seedling age of 30 days, cut off the petioles and bulbils of the virus-free seedlings in a sterile workbench, cut the petioles and bulbils into 3 to 5 segments, and inoculate them evenly on the in the above-mentioned induction medium. After 2 weeks of culture, callus tissue grew on the segment, and the segment was cut into about 5-10 small segments. Th...
Embodiment 2
[0053]Embodiment 2 adopts the method of the present invention to carry out breeding
[0054] Disinfection and sterilization of the culture container: a plant tissue culture box that can be autoclaved is used. The box is composed of a box body and a box cover. The overall height is 4.5cm, and the length and width are 25cm.
[0055] Medium preparation: the medium is a liquid MS induction medium without any auxin, see Table 1.
[0056] Inoculation: Select and cultivate strong virus-free seedlings with a seedling age of 40 days, cut off the petioles and bulbils of the virus-free seedlings in a sterile workbench, cut the petioles and bulbils into 3 to 5 segments, and inoculate them evenly on the In the induction medium mentioned above. After culturing for 1.5 weeks, callus tissue grew on the segment, and the segment was cut into 5-10 small segments. Small segments were inoculated at a density of 1.0×1.0 cm, and 240 segments were placed in each culture box, 10 boxes in total.
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Embodiment 3
[0059] Embodiment 3 adopts the method of the present invention to carry out breeding
[0060] Disinfection and sterilization of the culture container: a plant tissue culture box that can be autoclaved is used. The box is composed of a box body and a box cover. The overall height is 4.5cm, and the length and width are 25cm.
[0061] Medium preparation: the medium is a liquid MS induction medium without any auxin, see Table 1.
[0062] Inoculation: Select strong tissue-cultured virus-free seedlings with a seedling age of 35 days, cut off the petioles and bulbils of the virus-free seedlings in a sterile workbench, cut the petioles and bulbils into 3 to 5 segments, and divide them evenly. Inoculated into the above induction medium. After culturing for 1 week, callus tissue grew on the segment, and the segment was cut into 5-10 small segments. The cut sections were planted at a density of 1.3×1.3cm, and 230 sections were placed in each culture box, 10 boxes in total.
[0063] In...
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