Zostera marina somatic embryo induction method
A technology of somatic embryos and macrophylla, applied in horticultural methods, botanical equipment and methods, plant regeneration, etc., can solve problems such as patents and literature that have not been reported, and achieve improved surface disinfection effect, short acquisition time, and avoidance of Effects of risk of genetic mutation in cells
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Embodiment 1
[0016] Embodiment 1: a method for inducing eosinophila somatic embryos, its implementation steps include:
[0017] (1) Selection of explants: take the flower branch of Eelium eosinophila as the explant donor, take the healthy young spathe inflorescence, scrape off the attached organisms on the surface, wash it in sea water and transfer it to the ultra-clean workbench Inside, soak in 10% hydrogen peroxide solution for 15-20min, rinse with sterilized sea water for 3 times, peel off the bract leaves outside the spathe inflorescence to obtain a sterile inflorescence;
[0018] (2) Induction culture of somatic embryos: Cut the sterile inflorescences into 3-5mm long explant fragments, inoculate them in the induction medium, and cultivate them at 16°C, under dark conditions and under 1000lux light conditions, every half a month Transfer once. After 17 days, small protrusions could be seen on the inflorescence, and after about 30 days, these small protrusions could be seen to develop ...
Embodiment 2
[0019] Embodiment 2: a kind of induction method of eosinopsis somatic embryo, its implementation steps are:
[0020] (1) Selection of explants: take the flower branch of Eelium eosinophila as the explant donor, take the healthy young spathe inflorescence, scrape off the attached organisms on the surface, wash it in sea water and transfer it to the ultra-clean workbench Inside, soak in 10% hydrogen peroxide solution for 15-20min, rinse with sterilized sea water for 3 times, peel off the bract leaves outside the spathe inflorescence to obtain a sterile inflorescence;
[0021] (2) Induction culture of somatic embryos: Cut the sterile inflorescences into 3-5mm long explant fragments, inoculate them in the induction medium, culture them at 16-20°C in the dark, and transfer them every half a month . After 20 days, small protrusions can be seen on the inflorescence, and after about 30 days, these small protrusions can be seen to develop into somatic embryos, which do not go through ...
Embodiment 3
[0022] Embodiment 3: a kind of induction method of eosinopsis somatic embryo, its implementation steps are:
[0023] (1) Selection of explants: take the flower branch of Eelium eosinophila as the explant donor, take the healthy young spathe inflorescence, scrape off the attached organisms on the surface, wash it in sea water and transfer it to the ultra-clean workbench Inside, soak in 10% hydrogen peroxide solution for 15-20min, rinse with sterilized sea water for 3 times, peel off the bract leaves outside the spathe inflorescence to obtain a sterile inflorescence;
[0024] (2) Induction culture of somatic embryos: Cut the sterile inflorescences into 3-5mm long explant fragments, inoculate them in the culture medium, culture them at 16-20°C in the dark, and transfer them every half month. After 23 days, small protrusions could be seen on the inflorescence, and after about 34 days, these small protrusions could be seen to develop into somatic embryos, which did not go through t...
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