Bergenia purpurascens(hook.f.et Thoms.)Engl. tender leaf tissue culture rapid propagation method
A tissue culture fast propagation and rock cabbage technology, applied in the field of plant tissue culture, can solve the problems of low rhizome reproduction coefficient, low seedling emergence rate of rock cabbage, unfavorable rapid and mass propagation of seedlings, etc. high effect
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[0026] Step 1): Extraction and disinfection of explants
[0027] Select healthy, fresh unexpanded or newly expanded young leaves, rinse them with tap water, first sterilize them with 70% alcohol for 30 seconds, then sterilize them with 0.1% mercury liter solution for 6-7 minutes, and finally rinse them with sterile water for 3-4 times. Cut the leaves into about 1.0cm under sterile conditions in the ultra-clean bench 2 The block of is used as the explant to be inoculated;
[0028] Step 2): Callus Induction Culture
[0029] The size obtained by step 1) will be about 1.0cm 2 Inoculate the leaf pieces on the callus induction medium, culture in a constant temperature incubator at 23°C, 1500-2500Lx, light 12h / d, and form callus in 25-30d;
[0030] The callus induction medium is MS+2,4-D0.2mg / L+6-BA0.5mg / L+NAA0.4mg / L+activated carbon 3g / L; wherein MS is MS medium, which contains sucrose 30g / L, agar strip 8g / L, and its pH is 5.5-6.0.
[0031] Step 3): Adventitious bud induction c...
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