Medicinal anoectochilus Formosan tissue culture one-step seedling establishment fast replication method
A technology for tissue culture and clematis, which is applied in horticultural methods, botanical equipment and methods, cultivation, etc., can solve the problems of long cultivation time, high cost, and lack of development of clematis, and achieve good growth results
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Embodiment 1
[0034] 1) Medium preparation
[0035] (1) Preparation: take 1 / 2MS as the basic medium, add 6-BA2mg, NAA1.0mg, brassinolide 0.05mg, banana 100g, agar 6.5g and sucrose 25g per liter, the medium after mixing the above substances The pH value was adjusted to 5.6;
[0036] (2) Packing: Heat the prepared medium until the agar is completely dissolved, and evenly pack it into clean culture bottles while hot, about 50ml per bottle, and cover it after cooling slightly;
[0037] (3) Sterilization: put the culture bottle added with the culture medium into the autoclave for sterilization in time, the sterilization conditions are: sterilize at 121° C. and 105 kPa for 15 minutes, take out the culture bottle in time after sterilization, and cool it for later use.
[0038] 2) Explant treatment
[0039] (1) Cleaning: Select healthy plants that grow naturally and are free from diseases and insect pests, clean the plants with water added with a little soap powder, and then rinse with running wa...
Embodiment 2
[0051] 1) Medium preparation
[0052] (1) Preparation: take 1 / 2MS as the basic medium, add 6-BA 2mg, NAA 1.5mg, brassinolide 0.05mg, banana 100g, agar 6.5g and sucrose 25g per liter, and adjust the pH to 5.6;
[0053](2) Packing: Heat the prepared medium until the agar is completely dissolved, and evenly pack it into clean culture bottles while hot, about 50ml per bottle, and cover it after cooling slightly;
[0054] (3) Sterilization: put the culture bottle added with the culture medium into the autoclave for sterilization in time, the sterilization conditions are: sterilize at 121° C. and 105 kPa for 15 minutes, take out the culture bottle in time after sterilization, and cool it for later use.
[0055] 2) Explant treatment
[0056] (1) Cleaning: Select healthy plants that grow naturally and are free from diseases and insect pests, clean the plants with water added with a little soap powder, and then rinse with running water for 2 hours;
[0057] (2) Disinfection: Under as...
Embodiment 3
[0068] 1) Medium preparation
[0069] (1) Preparation: take 1 / 2MS as the basic medium, add 6-BA 2mg, NAA 1.5mg, brassinolide 0.05mg, banana 100g, agar 6.5g and sucrose 25g per liter, and adjust the pH to 5.6;
[0070] (2) Packing: Heat the prepared medium until the agar is completely dissolved, and evenly pack it into clean culture bottles, each bottle is about 50ml, and cover it after cooling slightly;
[0071] (3) Sterilization: put the culture bottle added with the culture medium into the autoclave for sterilization in time, the sterilization conditions are: sterilize at 121° C. and 105 kPa for 15 minutes, take out the culture bottle in time after sterilization, and cool it for later use.
[0072] 2) Explant
[0073] The more robust tissue culture sterile seedlings (plants) were selected as explants.
[0074] 3) Vaccination
[0075] Remove the leaves of the aseptic seedlings cultured under sterile conditions, cut the stems into several stem segments with a length of abou...
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