Scientific and effective Sichuan radix aconiti lateralis preparata breeding method
A scientific technology of Radix Aconiti, which is applied in the field of propagation of Radix Aconitiae, can solve the problems of poor disease resistance, low yield, instability, etc., and achieve the effects of poor disease resistance, high differentiation rate, high rooting rate, and high survival rate
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Embodiment 1
[0030] In this embodiment, the shoot tip of the Aconite plant in Pingwu Aconite Provenance Base of Sichuan was selected as the explant, and the callus was induced by tissue culture for rapid propagation, including the following main steps:
[0031] Step 1: Selection and disinfection of explants
[0032] In the Sichuan Pingwu Fuzi Provenance Base, in March, the shoot tip of the annual robust Aconitum plant was selected as the explant (as the inoculation material), and treated at a low temperature of 4°C for 3 days; rinsed with tap water, and treated with 75% alcohol for 15-15 20s, soak in 0.1% mercury chloride solution for 10-12min, pour off the mercury solution, and wash with sterile water for 4-5 times; peel off the stem tip and cut it into 0.2mm length, and set aside;
[0033] The second step: inoculation and induction of callus
[0034] Use MS as the basic medium, add NAA 0.1mg / L+6-BA1.0mg / L to the basic medium as the medium for inducing callus, and inoculate the explants ...
Embodiment 2
[0043] In this embodiment, the leaves of Aconite fruticosa plants in Sichuan Pingwu Aconite Provenance Base are selected as explants, and rapid propagation is carried out through tissue culture, including the following main steps:
[0044] Step 1: Selection and disinfection of explants
[0045] In the Sichuan Pingwu Aconite Provenance Base, in March, the leaves of the annual robust Aconitum plant were selected as explants (as inoculation materials), treated at a low temperature of 4°C for 3 days; rinsed with tap water, and treated with 70% alcohol for 15-20s , soak in 0.1% mercuric acid solution for 10-12 minutes, pour off the mercuric solution, and wash it with sterile water for 4-5 times; cut the leaves into 1cm×1cm squares for later use;
[0046] Step 2: Induction of Callus
[0047] Use MS as the basic medium, add NAA0.2mg / L+6-BA4.0mg / L to the basic medium as the medium for inducing callus, and inoculate the explants treated in the first step above by conventional methods ...
Embodiment 3
[0056] In this embodiment, the stem section of the Aconite plant and the stem section with axillary buds in the Sichuan Pingwu Aconite Provenance Base are selected as explants, and the callus is induced by tissue culture for rapid propagation, including the following main steps:
[0057] Step 1: Selection and disinfection of explants
[0058] In the Sichuan Pingwu Fuzi Provenance Base, in March, the stem section of the annual strong Aconite plant and the stem section with axillary buds were selected as explants (as inoculation materials), treated at a low temperature of 4°C for 3 days; rinsed with tap water, Treat with 70% alcohol for 15-20 seconds, soak in 0.1% mercuric acid solution for 10-12 minutes, pour out the mercuric acid solution, and wash it with sterile water for 4-5 times; cut the stems and stems with axillary buds into about 1.5cm, stand-by;
[0059] The second step: inoculation and induction of callus
[0060] Use MS as the basic medium, add NAA0.2mg / L+6-BA2.0m...
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