Tissue culture method for Aristolochia heterophylla
A technique of tissue culture and self-prevention, which is applied in the field of plant tissue culture, can solve the problems of low survival rate, unfavorable promotion of good varieties, and differences in medicinal ingredients, and achieve the effect of high germination rate, easy operation, and good growth of seedlings
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Embodiment 1
[0015] (1) Bud induction culture: take the Hanzhong anti-bud stem section as the explant, cut off the leaves, cut into 6 cm long sections with 3 axillary buds, soak them in washing powder solution for 5 minutes, and then wash them with soft hair Brush and gently scrub the surface of the explant to remove the dust and some bacteria on the surface, then rinse it with tap water for 1 hour, then place it in an ultra-clean workbench, first disinfect it with 75% ethanol for 5 seconds, then wash it with sterile water for 3 times, and then wash it with 0.1 % mercuric chloride solution for 10 minutes, rinsed with sterile water for 5 times, and then dried the water drops on the surface with sterile filter paper, then inoculated into the bud induction medium for bud induction, and cultured at 26°C for 4 days in total darkness after inoculation. Then place it under 11 hours of light every day, and cultivate it under the condition of 1200lx light intensity for 28 days, count its bud inducti...
Embodiment 2
[0020] (1) Bud induction culture: take Hanzhong anti-bud stems as explants, cut off the leaves, cut into 3 long segments with 6 axillary buds, soak them in washing powder solution for 16 minutes, and then use a soft brush Gently brush the surface of the explant to remove the dust and some bacteria on the surface, then rinse it with tap water for 3 hours and place it in an ultra-clean workbench, first disinfect it with 75% ethanol for 15 seconds, then wash it with sterile water for 6 times, and then wash it with 0.1% ethanol Mercuric chloride solution was sterilized for 15 minutes, rinsed with sterile water for 5 times, and then wiped dry the water drops on the surface with sterile filter paper, and then inoculated into bud induction medium for bud induction. Placed under the condition of 10 hours of light every day, and the light intensity was 1500lx, cultivated for 30 days, and counted its bud induction rate and growth situation, and the bud induction rate was 85%. The bud in...
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