Method for growing cell embryos of Dendrobium huoshanense
A technology of somatic embryos and Dendrobium huoshanense, applied in the field of plant tissue culture, can solve the problems of inconsistent developmental stages of somatic embryos, low survival rate of regenerated plants, large differences in size, etc., and achieve effective protection, medicinal value, and operation. simple craftsmanship
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Embodiment 1
[0027] A method for somatic embryogenesis of Dendrobium Huoshanense comprises the following steps:
[0028] Step 1, induction of sterile test-tube plantlets
[0029] Mature fruits of wild Dendrobium huoshanense produced in Taipingfan Township, Huoshan County, Anhui Province were taken, and the surface was disinfected with 1% sodium hypochlorite aqueous solution for 60 min, and then rinsed with sterile double distilled water for 3 times, and then the fruit was cut open and the seeds were taken out , and the seeds were sprinkled on MS solid medium, and cultivated for 7 months at a temperature of 22 ± 2°C, a light intensity of 2000 lux, and a daily light of 12 hours to obtain 4 cm long sterile test-tube plantlets of Dendrobium huoshanense, see figure 1 .
[0030] Step 2, induction of embryogenic callus
[0031] Take the morphological lower end of the nodal stem section of sterile test-tube plantlets, insert it into a solid permeable medium with a controlled oxidation-reduction...
Embodiment 2
[0037] A method for somatic embryogenesis of Dendrobium Huoshanense comprises the following steps:
[0038] Step 1. Induction of sterile test-tube seedlings: take the mature fruit of wild Dendrobium huoshanense produced in Taipingfan Township, Huoshan County, Anhui Province, first disinfect the surface with 1% sodium hypochlorite aqueous solution for 60 minutes, and then rinse with sterile double distilled water for 5 minutes. Then cut the fruit, take out the seeds, sprinkle the seeds on MS solid medium, and cultivate them for 7 months at a temperature of 22±2°C, a light intensity of 2500 lux, and 12 hours of light per day to obtain 5 cm long Huoshan Dendrobium sterile test-tube seedlings.
[0039] Step 2, induction of embryogenic callus: Take the morphological lower end of the nodal stem segment of the sterile test tube plantlet, insert it into a solid permeable medium with a controlled redox potential of -0.03 volts, and place it at a temperature of 22±2°C 1. Induced and cu...
Embodiment 3
[0043] A method for somatic embryogenesis of Dendrobium Huoshanense comprises the following steps:
[0044] Step 1. Induction of sterile test-tube seedlings: take the mature fruit of wild Dendrobium huoshanense produced in Taipingfan Township, Huoshan County, Anhui Province, first disinfect the surface with 1% sodium hypochlorite aqueous solution for 60 min, and then rinse with sterile double distilled water for 4 Then cut the fruit, take out the seeds, sprinkle the seeds on MS solid medium, and cultivate them for 6 months at a temperature of 22±2°C, a light intensity of 3000 lux, and 12 hours of light per day to obtain 6 cm long Huoshan Dendrobium sterile test-tube seedlings.
[0045] Step 2. Induction of embryogenic callus: take the morphological lower end of the nodal stem segment of the sterile test-tube plantlet, insert it into a solid permeable medium with a controlled redox potential of -0.02 volts, and place it at a temperature of 22±2°C , Induced and cultured in the ...
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