Method for improving germination rate of paphiopedilum seeds preserved at ultra-low temperature by using sodium hypochlorite to treat
A technology of cryopreservation and sodium hypochlorite, which is applied in the field of plant protection biology and biology, can solve the problem of low germination rate of Paphiopedilum seeds, and achieve the effect of improving the germination rate of seeds
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Embodiment 1
[0013] (1) Collection and cryopreservation of seeds
[0014] Select robust Paphiopedilum armeniacum S.C.Chen&F.Y.Liu plants for artificial self-pollination during the flowering stage, collect fully mature and uncracked capsules within 4 months after pollination, and use the capsules on the ultra-clean workbench. Soak in alcohol with a volume fraction of 70% for 30 seconds, then sterilize with 0.1% mercuric chloride solution for 20 minutes, rinse with sterile water for 4 times, cut the capsules, put 8 grams of powdery mature seeds into the sterilized diameter Dehydrate on sterile filter paper with a diameter of 12 cm in a 15 cm petri dish, and 15 grams of dried discolored silica gel have been placed under the filter paper in each petri dish. After putting in the seeds, seal the culture dish with parafilm and dehydrate for 96 hours. After the seeds were dehydrated, put the seeds into 2mL cryovials and put them into liquid nitrogen at -196°C for storage. Some of the unpreserved ...
Embodiment 2
[0018] (1) Collection and cryopreservation of seeds
[0019] Select the vigorous Paphiopedilum emersonii Koop.&P.J.Cribb plant to carry out artificial self-pollination during the flowering stage, collect mature and uncracked capsules within 7 months after pollination, and place the capsules on the ultra-clean workbench. Soak in alcohol with a volume fraction of 75% for 45 seconds, then sterilize with a mercury solution of 0.15% mass fraction for 15 minutes, rinse with sterile water for 5 times, cut the capsules, and put 10 grams of powdery mature seeds into the sterilized Dehydration was carried out on sterile filter paper with a diameter of 12 cm in a petri dish with a diameter of 15 cm, and 20 grams of dried discolored silica gel had been placed under the filter paper in each petri dish. After placing the seeds, seal the culture dish with parafilm and dehydrate for 72 hours. After the seeds were dehydrated, put the seeds into 2mL cryovials and put them into liquid nitrogen ...
Embodiment 3
[0023] (1) Collection and cryopreservation of seeds
[0024] Select robust Paphiopedilum helenae Aver. plants to carry out artificial self-pollination at the flowering stage, collect mature and uncracked capsules within 9 months after pollination, and use a volume fraction of 80% of the capsules on the ultra-clean workbench After soaking in alcohol for 30 seconds, sterilize with 0.2% mercuric chloride solution for 10 minutes, rinse with sterile water for 6 times, cut the capsules, and put 14 grams of powdery mature seeds into a sterilized 15 cm diameter petri dish 22 grams of dried discolored silica gel have been placed under the filter paper in each Petri dish. After placing the seeds, seal the culture dish with parafilm and dehydrate for 48 hours. After the seeds were dehydrated, put the seeds into 2mL cryovials and put them into liquid nitrogen at -196°C for storage. Some of the unpreserved dehydrated seeds were used to determine the water content, and the water content of...
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