Stachys sieboldii stem tip detoxification and rapid propagation technology
A technique for detoxification of the shoot tip and Lithopteryxa, which is applied in the technical field of detoxification and rapid propagation of the shoot tip of the Codonthodera, can solve the problems of low emergence rate, low regeneration rate of adventitious buds, long seedling period and the like, and achieves The effect of solving the problem of reproduction and supply, reducing the harm of virus disease and increasing the yield
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Embodiment 1
[0029] A kind of detoxification and rapid propagation technology of caddis silkworm stem tip, consisting of the following steps:
[0030] (1) Start-up culture of caddis silkworm rhizomes: use the underground rhizomes of caddis worm cultivated in the field as explants, sterilize with 0.12% mercury chloride for 15 minutes, and then inoculate them with various hormone types and ratios. The starter culture was carried out on the MS medium of MS+6-BA 0.7 mg / L + NAA 0.15 mg / L, and the adventitious buds could be directly induced through the axillary buds on the rhizomes.
[0031] (2) Proliferation culture of adventitious buds of caddis worm: first induce adventitious bud clusters through the axillary buds on the rhizomes, cut off the adventitious bud clusters for proliferation culture, and the composition of the medium is MS+6-BA3.0mg / L+GA 3 0.5mg / L; Adventitious bud elongation medium is MS+6-BA 0.8mg / L+ NAA 0.6 mg / L+ GA 3 0.8 mg / L.
[0032] (3) Shoot apex stripping and inoculation...
Embodiment 2
[0039] A kind of detoxification and rapid propagation technology of caddis silkworm stem tip, consisting of the following steps:
[0040] (1) Start-up culture of caddis silkworm rhizomes: use the underground rhizomes of caddis silkworms cultivated in the field as explants, sterilize with 0.1% mercury chloride for 18 minutes, and then inoculate them with different hormone types and ratios. Adventitious buds can be induced directly through the axillary buds on the rhizomes. The medium is MS+6-BA 1.0 mg / L + NAA 0.1 mg / L.
[0041] (2) Proliferation culture of adventitious buds of caddis worm: first induce adventitious bud clusters through the axillary buds on the rhizomes, cut off the adventitious bud clusters for proliferation culture, and the proliferation medium is MS+6-BA4.5 mg / L+ GA 3 1.0 mg / L; Adventitious bud elongation medium with MS+6-BA 1.5mg / L+ NAA 0.4 mg / L+ GA 3 1.0 mg / L.
[0042] (3) Shoot apex stripping and inoculation: Take the above-mentioned aseptic test tube s...
Embodiment 3
[0049] A kind of detoxification and rapid propagation technology of caddis silkworm stem tip, consisting of the following steps:
[0050] (1) Start-up culture of caddis silkworm rhizomes: use the underground rhizomes of caddis silkworms cultivated in the field as explants, sterilize with 0.06% mercury chloride for 25 minutes, and then inoculate them with different hormone types and ratios. Adventitious buds can be induced directly through the axillary buds on the rhizomes. The medium is MS+6-BA 1.8 mg / L + NAA 0.25 mg / L.
[0051] (2) Proliferation culture of adventitious buds of caddis worm: the adventitious bud clusters were first induced through the axillary buds on the rhizomes, and the adventitious bud clusters were cut off for proliferation culture. The proliferation medium was MS+6-BA 5.0 mg / L+ GA 3 1.8 mg / L; Adventitious bud elongation medium with MS+6-BA 2.8mg / L+ NAA 1.0mg / L+ GA 3 2.0 mg / L.
[0052] (3) Shoot apex stripping and inoculation: Take the above-mentioned as...
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