Rapid breeding method based on tissue culture for helleborus thibetanus
A technique of tissue culture and iron chopsticks, applied in horticultural methods, botany equipment and methods, horticulture, etc., can solve the problems of large market demand, limited supply of seedlings, low germination rate, etc., and achieve the maintenance of female parent traits and low cost The effect of reducing and increasing the reproduction speed
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Embodiment 1
[0034] A method for rapidly breeding iron chopsticks based on tissue culture, comprising the following steps:
[0035] (1) The preparation of the culture medium, including the components and contents of the culture medium at each stage of tissue culture:
[0036] 1.1. Bud induction medium: MS+BA 3mg / L+NAA 0.3mg / L;
[0037] 1.2. Adventitious bud proliferation medium: MS+6-BA 2.0mg / L+NAA 0.2mg / L;
[0038] 1.3. Strong seedling medium: MS+6-BA 1.0mg / L+NAA 0.1mg / L;
[0039] 1.4. Rooting medium: MS+NAA 0.2mg / L+IBA 0.2mg / L;
[0040] The pH of the above-mentioned various media is 5.8, add 30g / L sucrose, 6g / L agar, culture temperature is 22°C, light is 2000Lx;
[0041] (2) Tissue culture of iron chopsticks:
[0042] 2.1. Obtaining sterile materials
[0043] Iron chopsticks dig out the small buds above the ground in March in spring, wash them with tap water for 1 hour, put them on the ultra-clean workbench, soak them in 75% ethanol for 30 seconds, soak them in 1‰ mercury liter for ...
Embodiment 2
[0053] A method for rapidly breeding iron chopsticks based on tissue culture, comprising the following steps:
[0054] (1) The preparation of the culture medium, including the components and contents of the culture medium at each stage of tissue culture:
[0055] 1.1. Bud induction medium: MS+BA 1mg / L+NAA 0.1mg / L;
[0056] 1.2. Adventitious bud proliferation medium: MS+6-BA 1.0mg / L+NAA 0.1mg / L;
[0057] 1.3. Strong seedling medium: MS+6-BA 0.5mg / L+NAA 0.1g / L;
[0058] 1.4. Rooting medium: MS+NAA 0.1mg / L+IBA 0.1mg / L;
[0059]The pH of the above-mentioned various media is 5.8, add 30g / L sucrose, 6g / L agar, culture temperature is 21°C, light is 1900Lx;
[0060] (2) Tissue culture of iron chopsticks:
[0061] 2.1. Obtaining sterile materials
[0062] Iron chopsticks dig out the small buds above the ground in March in spring, wash them with tap water for 1 hour, put them on the ultra-clean workbench, soak them in 75% ethanol for 30 seconds, soak them in 1‰ mercury liter for 15...
Embodiment 3
[0072] A method for rapidly breeding iron chopsticks based on tissue culture, comprising the following steps:
[0073] (1) The preparation of the culture medium, including the components and contents of the culture medium at each stage of tissue culture:
[0074] 1.1. Bud induction medium: MS+BA 5mg / L+NAA 0.5mg / L;
[0075] 1.2. Adventitious bud proliferation medium: MS+6-BA 3.0mg / L+NAA 0.3mg / L;
[0076] 1.3. Strong seedling medium: MS+6-BA 1.5mg / L+NAA 0.2mg / L;
[0077] 1.4. Rooting medium: MS+NAA 0.3mg / L+IBA 0.3mg / L;
[0078] The pH of the above various media is 5.8, add 30g / L sucrose, 6g / L agar, culture temperature is 23°C, light is 2100Lx;
[0079] (2) Tissue culture of iron chopsticks:
[0080] 2.1. Obtaining sterile materials
[0081] Iron chopsticks dig out the small shoots of the aboveground part in March in spring, wash them with tap water for 1 hour, put them on the ultra-clean workbench, soak them in 75% ethanol for 30 seconds, soak them in 1‰ mercury liter for 1...
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