Tissue culture method of dianella ensifolia
A technology of tissue culture of Suga orchid japonica, applied in horticultural methods, botanical equipment and methods, plant regeneration, etc., can solve problems such as large market demand and limited supply of seedlings, so as to improve the propagation speed and seedling quality The effect of uniformity
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Embodiment 1
[0023] Procurement of sterile materials
[0024] Take the small buds that germinate from the base of Sugamophyllum japonica, wash them with tap water for 2 hours, put them on a clean bench, soak them in 75% ethanol for 30 seconds, soak them in 1‰ mercury liter for 15 minutes, wash them with sterile water 5-6 times, and put them on a clean bench. Blot the water on the surface with filter paper, cut the base of the buds into 1cm lengths, and inoculate them on the bud induction medium. The nutritional components of the medium are MS+6-BA1. The composition is 30g / L sucrose, 6g / L agar, the pH value of the medium is controlled at 5.8, the culture temperature is controlled at 24°C, and the light is 70μmol / ms, and the bud induction culture is carried out.
[0025] Bud differentiation and proliferation
[0026] Four weeks after the budlets were inoculated on the budlet induction medium, the budlets began to swell, and yellow-green protrusions appeared, and obvious callus tissue could ...
Embodiment 2
[0034] Procurement of sterile materials
[0035] Take the small buds that germinate from the base of Sugamophyllum japonica, wash them with tap water for 2 hours, put them on a clean bench, soak them in 75% ethanol for 30 seconds, soak them in 1‰ mercury liter for 15 minutes, wash them with sterile water 5-6 times, and put them on a clean bench. Blot the water on the surface with filter paper, cut the base of the buds into 1cm lengths, and inoculate them on the bud induction medium. The nutrient composition of the medium is MS+6-BA2. The composition is 30g / L sucrose, 6g / L agar, the pH value of the medium is controlled at 5.8, the culture temperature is controlled at 24°C, and the light is 70μmol / ms, and the bud induction culture is carried out.
[0036] Bud differentiation and proliferation
[0037] Four weeks after the budlets were inoculated on the budlet induction medium, the budlets began to swell, and yellow-green protrusions appeared, and obvious callus tissue could be ...
Embodiment 3
[0045] Procurement of sterile materials
[0046] Take the small buds that germinate from the base of Sugamophyllum japonica, wash them with tap water for 2 hours, put them on a clean bench, soak them in 75% ethanol for 30 seconds, soak them in 1‰ mercury liter for 15 minutes, wash them with sterile water 5-6 times, and put them on a clean bench. Blot the water on the surface with filter paper, cut the base of the buds into 1cm lengths, and inoculate them on the bud induction medium. The nutrient composition of the medium is MS+6-BA3. The composition is 30g / L sucrose, 6g / L agar, the pH value of the medium is controlled at 5.8, the culture temperature is controlled at 25°C, and the light is 80μmol / ms, and the bud induction culture is carried out.
[0047] Bud differentiation and proliferation
[0048] Four weeks after the budlets were inoculated on the budlet induction medium, the budlets began to swell, and yellow-green protrusions appeared, and obvious callus tissue could be ...
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