Rapid breeding method for tissue culture of bambusa texlitis
A technology of tissue culture and green bamboo, which is applied in the field of plant cultivation, can solve the problems such as not easy to harden, and achieve the effect of high rooting rate, low energy consumption and high quality
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Embodiment 1
[0009] Take the tender stems of 2 nodes of Bambusa vegetalis, remove the leaves and terminal buds with a length of about 3mm, wash them in 20% bleach solution for 15 minutes, put 9% calcium hypochlorite on the ultra-clean workbench, and add two drops of Tween, Treat for 16 minutes, rinse with sterile water for 5 times, disinfect the stems of green bamboo shoots, insert WPM+ZT3mg / L+NAA0.1mg / L+ Guangdamycin 15mg / L+0.65% agar+30g / L sucrose for culture The buds were induced in the medium, pH5.80, light intensity 2700lx, photoperiod 13h / d, temperature 27℃, and the induced axillary buds were put into WPM+BAP0.3mg / L+Cad1.5mg / L+cysteine 100mg / Proliferate clustered buds in L+0.65% agar+30g / L sucrose medium, pH5.80, light 3500lx, photoperiod 15h / d, temperature 27℃, cultured clustered shoots were inserted into LS+NAA0.1mg / L +Cad1mg / L, add 0.65% agar, 50g / L sucrose to induce rooting, pH5.80, light 10000lx, photoperiod 18h / d, temperature 28°C, the rooting rate was calculated after one m...
Embodiment 2
[0011] Take the tender stems of 2 nodes of Bambusa vegetalis, remove the leaves and terminal buds with a length of about 3mm, wash them in 20% bleach solution for 15 minutes, put 9% calcium hypochlorite on the ultra-clean workbench, and add two drops of Tween, Treat for 16 minutes, rinse with sterile water for 5 times, disinfect the stems of green bamboo shoots, insert WPM+ZT3mg / L+NAA0.1mg / L+ Guangdamycin 15mg / L+0.65% agar+30g / L sucrose for culture The buds were induced in the medium, pH5.80, light intensity 2700lx, photoperiod 13h / d, temperature 27°C, the induced axillary buds were put into WPM+BAP0.4mg / L+Cad2mg / L+cysteine 100mg / L+ Proliferate clustered buds in 0.65% agar + 30g / L sucrose medium, pH 5.80, light 3500lx, photoperiod 15h / d, temperature 27°C, cultured clustered shoots were inserted into LS+NAA0.1mg / L+Cad1mg / L, add 0.65% agar, 50g / L sucrose to induce rooting, pH 5.80, light 10000lx, photoperiod 18h / d, temperature 28°C, the rooting rate was calculated after one m...
Embodiment 3
[0013] Take the tender stems of 2 nodes of Bambusa vegetalis, remove the leaves and terminal buds with a length of about 3mm, wash them in 20% bleach solution for 15 minutes, put 9% calcium hypochlorite on the ultra-clean workbench, and add two drops of Tween, Treat for 16 minutes, rinse with sterile water for 5 times, disinfect the stems of green bamboo shoots, insert WPM+ZT3mg / L+NAA0.1mg / L+ Guangdamycin 15mg / L+0.65% agar+30g / L sucrose for culture The buds were induced in the medium, pH5.80, light intensity 2700lx, photoperiod 13h / d, temperature 27°C, and the induced axillary buds were put into WPM+BAP0.5mg / L+Cad2mg / L+cysteine 100mg / L+ Proliferate clustered buds in 0.65% agar + 30g / L sucrose medium, pH 5.80, light 3500lx, photoperiod 15h / d, temperature 27°C, cultured clustered shoots were inserted into LS+NAA0.1mg / L+Cad1 .2mg / L, add 0.65% agar, 50g / L sucrose to induce rooting, pH 5.80, light 10000lx, photoperiod 18h / d, temperature 28°C, the rooting rate was calculated after...
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