Tissue culture and rapid propagation method for sspindus mukurossi
A technology for tissue culture, fast propagation and Sapindus japonica, applied in the field of plant tissue culture, can solve problems such as lack of supply of fine seedlings, restrictions on natural renewal and industrial application of Sapindus japonica, and lag in breeding of fine seeds, and reduce the natural environment. The degree of dependence, the effect of keeping the excellent characteristics unchanged, and reducing the production cost
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Embodiment 1
[0018] (1) Disinfection of explants: Sampling should be carried out on sunny days for more than 3 consecutive days and when there is no dew on the branches. The sampling time is between 9 and 10 in the morning. Take the young stems with axillary buds on the branches of Sapindus sativa in the same year as explants, wash off the dirt on the surface, soak in 3% washing powder dilution solution for more than 30 minutes, and then rinse under running water for more than 2 hours, turn to Go to the ultra-clean workbench for sterilization. Soak in 70% ethanol solution for 60s, rinse with sterile water for 5 times, then disinfect with 0.1% mercuric solution for 8 minutes, and then rinse the explants with sterile water until there is no foam. Finally, place the sterilized scales on sterile filter paper to blot the surface moisture for later use.
[0019] (2) Adventitious bud induction: Cut the stem segment with axillary buds about 2cm long in step (1) and inoculate it into the induc...
Embodiment 2
[0024] (1) Disinfection of explants: Sampling should be carried out on sunny days for more than 3 consecutive days and when there is no dew on the branches. The sampling time is between 9 and 10 in the morning. Take the young stems with axillary buds on the branches of Sapindus sativa in the same year as explants, wash off the dirt on the surface, soak in 3% washing powder dilution solution for more than 30 minutes, and then rinse under running water for more than 2 hours, turn to Go to the ultra-clean workbench for sterilization. Soak in 75% ethanol solution for 30s, rinse with sterile water for 5 times, then disinfect with 0.15% mercuric solution for 5 minutes, and then rinse the explants with sterile water until there is no foam. Finally, place the sterilized scales on sterile filter paper to blot the surface moisture for later use.
[0025] (2) Adventitious bud induction: Cut the stem segment with axillary buds about 2cm long in step (1) and inoculate it into the indu...
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