Rapid propagation method for tissue culture of momordica cochinchinensis (Lour.) Spreng
A technique for tissue culture and Momordica charcoal is applied in the field of plant cultivation and can solve the problems of low reproduction rate, long growth cycle and high cost
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Embodiment 1
[0009] Select smooth and plump seeds, soak them in concentrated sulfuric acid for 1 hour, rinse them repeatedly with tap water and sow them in flower pots with fine sand as the substrate, place the flower pots in a place with sufficient light, and place the leaves of the cultivated wood beetle seedlings on the ground with clean gauze. Wash in water with detergent, soak in 10% hydrogen peroxide for 6 minutes, rinse with sterile water 5 times, cut into small pieces of 0.5cm×0.5cm and put them into MS+IBA0.02mg / L+ZT3mg / L medium , add 0.7% agar, 35g / L sucrose to induce callus, pH5.85, culture in darkroom, temperature 27℃, put the induced callus into ER+IAA0.1mg / L+5mg / L2ip+PVP0. Carry out callus differentiation in 2g / L+0.7% agar+35g / L sucrose medium, pH 5.85, light 3000lx, temperature 27°C, take the sprouts out of the culture bottle and put them in 0.3% sodium sulfate solution Soak for 3 minutes, rinse with sterile water, put it into the sterilized perlite substrate, pour MS nutrie...
Embodiment 2
[0011] Select smooth and plump seeds, soak them in concentrated sulfuric acid for 1 hour, rinse them repeatedly with tap water and sow them in flower pots with fine sand as the substrate, place the flower pots in a place with sufficient light, and place the leaves of the cultivated wood beetle seedlings on the ground with clean gauze. Wash in water with detergent, soak in 10% hydrogen peroxide for 6 minutes, rinse with sterile water 5 times, cut into small pieces of 0.5cm×0.5cm and put them into MS+IBA0.02mg / L+ZT3mg / L medium , add 0.7% agar, 35g / L sucrose to induce callus, pH5.85, culture in darkroom, temperature 27°C, put the induced callus into ER+IAA0.15mg / L+6mg / L2ip+PVP0. Carry out callus differentiation in 25g / L+0.7% agar+35g / L sucrose medium, pH 5.85, light 3000lx, temperature 27°C, take the sprouts out of the culture bottle and put them in 0.3% sodium sulfate solution Soak for 3 minutes, rinse with sterile water, put it into the sterilized perlite substrate, pour MS nut...
Embodiment 3
[0013] Select smooth and plump seeds, soak them in concentrated sulfuric acid for 1 hour, rinse them repeatedly with tap water and sow them in flower pots with fine sand as the substrate, place the flower pots in a place with sufficient light, and place the leaves of the cultivated wood beetle seedlings on the ground with clean gauze. Wash in water with detergent, soak in 10% hydrogen peroxide for 6 minutes, rinse with sterile water 5 times, cut into small pieces of 0.5cm×0.5cm and put them into MS+IBA0.02mg / L+ZT3mg / L medium , add 0.7% agar, 35g / L sucrose to induce callus, pH5.85, culture in darkroom, temperature 27℃, put the induced callus into ER+IAA0.1mg / L+6mg / L2ip+PVP0. Carry out callus differentiation in 2g / L+0.7% agar+35g / L sucrose medium, pH 5.85, light 3000lx, temperature 27°C, take the sprouts out of the culture bottle and put them in 0.3% sodium sulfate solution Soak for 3 minutes, rinse with sterile water, put it into the sterilized perlite substrate, pour MS nutrie...
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