Culturing technology for upright-ladybell-root in-vitro regeneration tissue
A technology of in vitro regeneration and tissue culture, which is applied in the field of plant tissue culture, can solve the problems of low seed germination rate, failure to meet the needs of Nansha ginseng seedlings, and unfavorable promotion of good varieties, and achieve the effect of meeting the demand for production seed quantity
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Embodiment 1
[0015] (1) Bud induction culture: use the isolated regenerated bud stem section of Nansha Radix as explants, cut off the leaves, cut into 4.8 long sections with 4 axillary buds, soak them in washing powder solution for 4 minutes, and then wash them with soft water. Gently scrub the surface of the explant with a brush to remove the dust and some bacteria on the surface, then rinse it with tap water for 2 hours, then place it in an ultra-clean workbench, first disinfect it with 75% ethanol for 4 seconds, then wash it twice with sterile water, and then use Disinfect with 0.2% mercuric chloride solution for 9 minutes, rinse with sterile water for 3 times, then dry the water drops on the surface with sterile filter paper, then inoculate into bud induction medium for bud induction, and culture in total darkness at 27°C for 2 days after inoculation , then 9 hours of light every day, and the light intensity was cultivated for 29 days under the condition of 1400lx, and the bud induction...
Embodiment 2
[0020] (1) Bud induction culture: Use the stem section of Nansha ginseng with buds as explants, cut off the leaves, cut into 8.0 long segments with 6 axillary buds, soak them in washing powder solution for 13 minutes, and then gently brush them with a soft brush. Lightly scrub the surface of the explant to remove the dust and part of the bacteria on the surface, then rinse it with tap water for 2 hours, then place it in an ultra-clean workbench, first disinfect it with 75% ethanol for 18 seconds, then wash it with sterile water for 8 times, and then use 0.1% L Mercury solution was sterilized for 18 minutes, rinsed with sterile water for 7 times, and then wiped dry the water droplets on the surface with sterile filter paper, and then inoculated into bud induction medium for bud induction. Illuminated for 13 hours, and the light intensity was cultivated for 33 days under the condition of 1800lx, and the bud induction rate and growth situation were counted, and the bud induction r...
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