Rapid propagation method of cyclobalanopsis glauca
A green and fast technology, applied in the field of plants, can solve the problems of high survival rate, low production cost and short growth cycle of tissue culture methods, and achieve the effects of short cycle, low pollution and large yield.
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Embodiment 1
[0009] Freshly extracted Qinggang, cut into small sections of about 2cm with axillary buds or terminal buds, first soak in bleach for 3 minutes, remove surface stains with a brush, rinse with running water for 45 minutes, and treat with 400 μg / g benzyl ammonium blue solution on a clean bench for 20 minutes, Rinse 5-7 times with sterile water, and insert the sterilized Qinggang bud stem section into the culture medium formula is N 6 +6-BA1.0mg / L+NAA0.1mg / L induction medium for axillary bud induction culture, added sugar 30g / L, agar 6.5g / L, pH5.8, light 2500lx, temperature 26±1℃, induced Put the buds into the medium 1 / 2N 6 +IAA0.1mg / L+50mg / L tomato juice for proliferation culture, add sugar 30g / L, agar 6.5g / L, pH5.8, light 3000lx, temperature 26±1℃, put the clustered shoots cultured for rooting Medium 3 / 4N 6 +NAA0.05mg / L+80mg / L cysteine+sucrose 20g / L, agar 6.5g / L, pH5.8, light 4000lx, temperature 28°C, test-tube plantlets about 5cm long, taken out from the culture bottle, 0.5...
Embodiment 2
[0011] Freshly extracted Qinggang, cut into small sections of about 2cm with axillary buds or terminal buds, first soak in bleach for 3 minutes, remove surface stains with a brush, rinse with running water for 45 minutes, and treat with 400 μg / g benzyl ammonium blue solution on a clean bench for 20 minutes, Rinse 5-7 times with sterile water, and insert the sterilized Qinggang bud stem section into the culture medium formula is N 6 +6-BA1.0mg / L+NAA0.1mg / L induction medium for axillary bud induction culture, added sugar 30g / L, agar 6.5g / L, pH5.8, light 2500lx, temperature 26±1℃, induced Put the buds into the medium 1 / 2N 6 +IAA0.3mg / L+50mg / L tomato juice for proliferation culture, add sugar 30g / L, agar 6.5g / L, pH5.8, light 3000lx, temperature 26±1°C, put the clustered shoots cultivated for rooting Medium 3 / 4N 6 +NAA1.0mg / L+100mg / L cysteine+sucrose 20g / L, agar 6.5g / L, pH5.8, light 4000lx, temperature 28°C, test-tube plantlets about 5cm long, taken out from the culture bottle, ...
Embodiment 3
[0013] Freshly extracted Qinggang, cut into small sections of about 2cm with axillary buds or terminal buds, first soak in bleach for 3 minutes, remove surface stains with a brush, rinse with running water for 45 minutes, and treat with 400 μg / g benzyl ammonium blue solution on a clean bench for 20 minutes, Rinse 5-7 times with sterile water, and insert the sterilized Qinggang bud stem section into the culture medium formula is N 6 +6-BA1.0mg / L+NAA0.1mg / L induction medium for axillary bud induction culture, added sugar 30g / L, agar 6.5g / L, pH5.8, light 2500lx, temperature 26±1℃, induced Put the buds into the medium 1 / 2N 6 +IAA0.3mg / L+50mg / L tomato juice for proliferation culture, add sugar 30g / L, agar 6.5g / L, pH5.8, light 3000lx, temperature 26±1°C, put the clustered shoots cultivated for rooting Medium 3 / 4N 6 +NAA0.05mg / L+90mg / L cysteine+sucrose 20g / L, agar 6.5g / L, pH5.8, light 4000lx, temperature 28°C, test-tube plantlets about 5cm long, taken out from the culture bottle, ...
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