Tissue culture quick reproduction method for dendrobium chrysotoxum lindl bud tips
A technology for tissue culture and Dendrobium Dendrobium, which is applied in the field of rapid propagation of Dendrobium Dendrobium sprout tip tissue culture, can solve problems that hinder the development and utilization of Dendrobium Dendrobium Dendrobium, the protection of native species of Dendrobium Dendrobium, the high degree of separation of the characters of the descendants of Dendrobium Dendrobium, and the difficulty in solving the problems. Realize the problems of plants with the same traits, and achieve the effect of less investment, short cycle and easy operation
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Embodiment 1
[0036] Select 5-8 cm long young shoots, remove the packs, rinse them with tap water and cut them into two sections, soak them in 70% alcohol for 15 seconds on a clean bench, and then sterilize them with 0.1% mercury solution After washing 5 times with sterile water for 8 minutes, absorb the residual water with sterile filter paper, and cut 1-2 cm long stems with lateral bud tips to inoculate the induction medium with 1 / 2MS+6-BA(6-benzyl Amino adenine) 0.5㎎ / L+AD (Adenine) 1.0㎎ / L+AgNO 3 5.0 ㎎ / L +10.0% coconut juice+5.0g / L activated carbon, light intensity 1500~2000lx, light 10 hours / day, temperature 25~28℃. After 40 to 55 days of cultivation, new shoots are formed and grow. The clumping buds obtained by cultivating the bud tips are cut and transferred to the clumping bud propagation medium 1 / 2MS+6-BA (6-benzylamino adenine) 1.0㎎ / L+AD (adenine) 0.5㎎ / L +AgNO 3 5.0㎎ / L +10.0% coconut juice+5.0g / L activated carbon, under the conditions of light intensity 1500~2000lx, light for 10 h...
Embodiment 2
[0038] Select 5-8 cm long young shoots, remove the packs, rinse them with tap water and cut them into two sections, soak them in 70% alcohol for 30 seconds on a clean bench, and then sterilize them with 0.1% mercury solution After washing with sterile water for 6 times for 10 minutes, absorb the residual water with sterile filter paper, and cut 1-2 cm long stems with lateral bud tips to inoculate the induction medium with 1 / 2MS+6-BA(6-benzyl Amino adenine) 0.75㎎ / L+AD (Adenine) 1.25㎎ / L+AgNO 3 7.5 ㎎ / L +15.0% coconut water+7.5g / L activated carbon, light intensity 1500~2000lx, light 11 hours / day, temperature 25~28℃. After 40 to 55 days of cultivation, new shoots are formed and grow. The clumping buds obtained by cultivating the bud tips are cut and transferred to the clumping bud propagation medium 1 / 2MS+6-BA (6-benzylamino adenine) 1.5㎎ / L+AD (adenine) 0.75㎎ / L +AgNO 3 7.5㎎ / L +15.0% coconut juice+7.5g / L activated carbon, under the conditions of light intensity 1500~2000lx, light ...
Embodiment 3
[0040] Select 5-8 cm long young shoots, remove the packs, rinse them with tap water and cut them into two sections, soak them in 70% alcohol for 45 seconds on an ultra-clean workbench, and then sterilize them with 0.1% mercury solution After rinsing with sterile water for 8 times for 12 minutes, use sterile filter paper to absorb the residual water, and cut 1-2 cm long stems with lateral bud tips to inoculate the induction medium with 1 / 2MS+6-BA(6-benzyl Amino adenine) 1.0㎎ / L+AD (Adenine) 1.5㎎ / L+AgNO 3 10.0 ㎎ / L +20.0% coconut juice + 10.0g / L activated carbon, light intensity 1500~2000lx, light 12 hours / day, temperature 25~28℃. After 40 to 55 days of cultivation, new shoots are formed and grow. The clump buds obtained by cultivating the bud tips are cut out and transferred to the clump bud propagation medium 1 / 2MS+6-BA(6-benzylamino adenine) 3.0㎎ / L+AD(adenine) 1.0㎎ / L +AgNO 3 10.0㎎ / L +20.0% coconut juice + 10.0g / L activated carbon, at light intensity of 1500~2000lx, light for ...
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