A method for rapid propagating China red nouelia
A fast and fast technology of Rhizoma sinensis, which is applied in the field of plant regeneration of tissue culture technology, can solve the problems of slow multiplication speed of tissue culture seedlings, low survival rate of transplanting, difficulty in rooting, etc., and achieves simple and easy cultivation method, good growth effect, light browning effect
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Embodiment 1
[0034] (1) Selection of explants
[0035] Use grafting or cuttings to propagate a small amount of Sinus sinensis seedlings, spray fungicides regularly, and plant Sinus sinensis in the greenhouse in late January or early February of the following year. At the end of February and early March, the new shoots grow to 15-25 cm, cut the new shoots and cut them into 1.5-2.5cm stem segments, rinse them with running water first, shake them with 70% alcohol for 15-50 seconds on an ultra-quiet platform, and then place them in 0.2% mercury chloride and 10% calcium hypochlorite for 3-8 minutes, and finally rinsed with sterile water for 3-5 times, as explants for tissue culture and rapid propagation of Red Sinensis; the experimental results showed that using 0.2% mercuric chloride Used in conjunction with 10% calcium hypochlorite, the disinfection effect is good, the pollution rate is only 24.2%, and the pollution rate is low. The new shoots cultivated in the greenhouse in February and Marc...
Embodiment 2
[0045]In the cultivation process of tissue culture seedlings in this embodiment, the inoculation medium used is 1 / 2MS basic medium with the addition of 0.5mg / L of BA and 0.1mg / L of NAA; the used expansion medium is 1 / 2MS basic The BA of 1.0mg / L and the NAA of 0.1mg / L are added to the culture medium; The rooting medium used is the IBA of 0.5mg / L added to the 1 / 2MS basal medium; In the present embodiment, other cultivation steps are the same as in Example 1 .
Embodiment 3
[0047] In the cultivation process of the tissue culture seedlings in this embodiment, the inoculation medium used is 1 / 2MS basic medium with the addition of 1.5mg / L of BA and 1.0mg / L of NAA; the used expansion medium is 1 / 2MS basic The BA of 2.5mg / L and the NAA of 1.0mg / L are added in the medium; The rooting medium used is the IBA of 2.5mg / L added to the 1 / 2MS basic medium; In the present embodiment, other cultivation steps are identical with embodiment 1 .
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