In-vitro embryo cultivation method for measuring vitality of cynomorium seeds
A viability and embryo culture technology, applied in horticultural methods, botanical equipment and methods, applications, etc., can solve the problems of not completely eliminating seed dormancy, declining seed viability, low seed germination rate, etc. , fast and safe rejection, good repeatability
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Embodiment 1
[0050] The first isolated embryo culture method for measuring the viability of Cynomorium cynomorium seeds comprises the following steps:
[0051] a) take wild fully mature Cynomorium cynomorium seeds 500g;
[0052] b) Cynomorium seeds are put into the cleaning machine, cleaned at a wind speed of 12.6m / s, then coarsely screened with a 1.62mm sieve, and then finely screened with a 0.60mm sieve to obtain clean seeds;
[0053] c) Removal of appendages: Soak in 1% NaOH solution for 3 minutes under stirring to obtain seeds without appendages, and the removal rate reaches 100%;
[0054] d) Hard fruit removal: Randomly select 400 seeds without appendages obtained in step c), conduct 4 repeated experiments of 100 seeds each time, and treat Cynomorium cynomorium seeds with 1mol / L NaOH solution for 5 hours;
[0055] e) Remove the seed coat and take out the seed kernel: squeeze the peel with tweezers, take out the seed kernel, and obtain the peeled seed kernel;
[0056] f) Culture of i...
Embodiment 2
[0060] The second method for culturing in vitro embryos used for the determination of Cynomorium seed viability comprises the following steps:
[0061] a) take wild fully mature Cynomorium cynomorium seeds 500g;
[0062] b) Clarity treatment: put Cynomorium cynomorium seeds into the cleaning machine, clean them with a wind speed of 10m / s, then use a 1.5 sieve to carry out coarse screening to the seeds, and then use a 0.40mm sieve to carry out fine screening to the seeds to obtain clean seed;
[0063] c) Removal of appendages: scald the seeds with hot water at 90°C, cool to room temperature and ensure that the seeds are soaked in water for 24 hours, then rub with nylon gauze, the removal rate is 96.7%;
[0064] d) Hard fruit removal: Randomly select 400 seeds without appendages obtained in step c), and conduct 4 repeated experiments of 100 seeds each time, and treat Cynomorium cynomorium seeds with 1.5mol / L NaOH solution for 4 hours;
[0065] e) Remove the seed coat and take ...
Embodiment 3
[0070] The third method for in vitro embryo culture for Cynomorium seed viability assay comprises the following steps:
[0071] a) take wild fully mature Cynomorium cynomorium seeds 500g;
[0072] b) Clarity treatment: Put Cynomorium cynomorium seeds into the cleaning machine, clean them with a wind speed of 15m / s, then use a 1.8 sieve to carry out coarse screening to the seeds, then use a 0.8mm sieve to carry out fine screening to the seeds to obtain clean seed;
[0073] c) Removal of appendages: scald the seeds with hot water at 100°C, cool to room temperature and ensure that the seeds are soaked in water for 24 hours, then rub with nylon gauze, the removal rate is 94%;
[0074] d) Hard fruit removal: Randomly select 400 seeds without appendages obtained in step c), conduct 4 repeated experiments of 100 seeds each time, and treat Cynomorium cynomorium seeds with 2.0mol / L NaOH solution for 3 hours;
[0075] e) Remove the seed coat and take out the seed kernel: squeeze the p...
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