A method for tissue culture and rapid propagation of Primula huaiji
A technology of primula moss and tissue culture, which is applied in the fields of botany equipment and methods, horticultural methods, plant regeneration, etc., and can solve the problems of tissue culture and seedling propagation of primula moss in Huaiji, slow cutting propagation speed, Low seed germination rate and other problems, to achieve the effect of resource protection and sustainable utilization, simple and affordable operation, and good growth
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Embodiment 1
[0022] 1. Disinfection of explants and induction culture of the first generation: Cut the thick young leaves of Primula huaiji as explants during the growing season, rinse with detergent for 20 minutes, rinse with running water for 30 minutes, and then place them on the ultra-clean workbench. Soak in 75% ethanol solution by volume fraction for 30s, mass fraction 0.1% HgCl 2 Disinfect the solution for 4 minutes, rinse with sterile water for 5 times, dry the surface water with sterile filter paper, cut the leaves into small pieces of 1.0cm×2.0cm, inoculate them on the primary induction medium, and cultivate them at a temperature of 25±2°C. The light intensity is 1500lx, and the light time is 12h / d. After culturing for about 30 days, calluses began to grow around the cut pieces and a few buds germinated. After continuing to cultivate for about 38 days, many young shoots germinated on the callus. The success rate of disinfection is 85%. The primary induction medium is as follow...
Embodiment 2
[0027] 1. Disinfection of explants and induction culture of the first generation: Cut the thick young leaves of Primula huaiji as explants during the growing season, rinse with detergent for 20 minutes, rinse with running water for 30 minutes, and then place them on the ultra-clean workbench. Soak in 75% ethanol solution by volume fraction for 30s, mass fraction 0.1% HgCl 2 Disinfect the solution for 5 minutes, rinse 6 times with sterile water, dry the surface water with sterile filter paper, cut the leaves into small pieces of 0.5cm×1.0cm, inoculate them on the primary induction medium, and cultivate them at a temperature of 25±2°C. The light intensity is 1500lx, and the light time is 12h / d. Around the 19th day of culture, the callus began to grow around the cutting and a little bud germinated. A large number of young shoots germinated on the callus after continuing to cultivate for about 27 days. The success rate of disinfection is 85%. The primary induction medium is as ...
Embodiment 3
[0032] 1. Disinfection of explants and induction culture of the first generation: Cut the thick young leaves of Primula huaiji as explants during the growing season, rinse with detergent for 20 minutes, rinse with running water for 30 minutes, and then place them on the ultra-clean workbench. Soak in 75% ethanol solution by volume fraction for 30s, mass fraction 0.1% HgCl 2 Disinfect the solution for 4 minutes, rinse with sterile water for 5 times, dry the surface water with sterile filter paper, cut the leaves into small pieces of 1.0cm×2.0cm, inoculate them on the primary induction medium, and cultivate them at a temperature of 25±2°C. The light intensity is 1500lx, and the light time is 12h / d. After 22 days or so of cultivation, calluses began to grow around the cut pieces and a few buds germinated. Continue to cultivate for about 30 days and germinate many tiny young shoots on the callus. The success rate of disinfection is 85%. The primary induction medium: each liter ...
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