A kind of tissue culture method of Qingniao Shou
A technology of tissue culture and longevity of blue birds, which is applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of prolonged production cycle, low success rate, and few materials.
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Embodiment 1
[0025] A method for tissue culture of Jade Bird Shou, comprising the steps of:
[0026] 1) Materials: use the female parent of Jade Bird Shou (such as figure 1 Shown) fleshy leaves as explants, use cotton thread to strip the selected Jade Bird Shou plant leaves into individual leaves, first clean the Jade Bird Shou leaves with a detergent containing 60% linear alkylbenzene sulfonate sodium, and pour them out after cleaning. Remove the washing liquid, then rinse the leaves washed with washing powder under tap water for 30 minutes, put the leaves at 4°C overnight, and rinse the leaves under running water for 2 hours the next day.
[0027] 2) Sterilization of materials: Place the explants of Jade Bird Shou that have been cleaned above in a beaker on a clean bench and soak them in 75% alcohol for 30 seconds, rinse them with sterile water for 2-3 times after soaking, and then rinse them with sterile water. Quickly pour the cultured part of Jade Bird Shou into 0.1% mercuric acid so...
Embodiment 2
[0032] The disinfection time of mercuric chloride has a great influence on the bacterial contamination of explants. Short disinfection time will result in incomplete sterilization and serious bacterial contamination; too long disinfection time will result in excessive sterilization and browning of explants. And die. Therefore, use the optimal disinfection time to provide sterile explants for later callus induction. The experiment was carried out in three batches, each batch had the same number of inoculations, and the average of the experimental results of the three batches was taken, and Table 1 was obtained. It can be seen from Table 1 that the optimal disinfection time for mercuric chloride with a concentration of 0.1% is 5 minutes. The sterilizing result of 3 minutes is not ideal, the bacterial contamination is serious, the bacterial contamination rate reaches 100%, and the explants eventually die due to bacterial contamination; the sterilization time of 4.5 minutes can a...
Embodiment 3
[0036] Different concentrations of the same growth hormone have different effects, too high or too low concentration may cause callus non-induction behavior or cause the induction time to be too long.
[0037] The sterile explants in the MS medium were transferred to the medium of MS+6-BA 1.0 mg / L+NAA 0.1-0.4 mg / L, pH 5.8-6.0. The experiment was carried out in three batches, each batch had the same number of inoculations, and the average number of the three batches of experiments was taken, and Table 2 was obtained. It can be seen from Table 2 that NAA of 0.1mg / L and 0.4mg / L failed to induce callus, and the induction rate of NAA concentration of 0.2mg / L and 0.3mg / L could reach 50%, but it was obvious that 0.2mg / L NAA in L is the most favorable hormone concentration for callus induction, because it can grow callus in the shortest time.
[0038] Table 2 The results of different concentrations of NAA inducing the callus of Qingtiao Shou
[0039]
[0040]
[0041] The call...
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