Rapid breeding method for malus micromalus tissue culture
A technology of tissue culture and Begonia, which is applied in the field of rapid plant propagation, can solve the problems of small reproduction coefficient, limited success of tissue culture to individual species, slow research progress, etc., and achieves the effect of superior tissue growth conditions and avoiding tissue browning
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Embodiment 1
[0017] 1. Inoculate the young shoots of crabapple plants on the induction medium to induce initial protocorms the size of sesame seeds; the specific composition and content of the induction medium are: KN0 3 1200mg / L, NH 4 N0 3 1000mg / L, KH 2 P0 4 110mg / L, MgS0 4 230mg / L, CaCl 2 200mg / L, KI 0.83mg / L, MnS0 4 22.3mg / L, ZnS0 8.6mg / L, Na 2 -EDTA 37.3mg / L, FeS0 4 27.8mg / L, 20-30mg / L sucrose, 0.01-0.5mglL 6-BA, 0.01g / L activated carbon, 4g / L agarose, pH 5.0;
[0018] Two, the initial protocorm is transferred to the proliferation medium for proliferation culture, every four weeks, after the proliferated initial protocorm is cut, subculture is carried out, so that the protocorm proliferates rapidly, and the medium used for subculture is the same as described The proliferation medium is the same; the proliferation medium is a liquid-solid two-phase medium with improved MS as the basic medium and additional components, in which the upper layer is a liquid phase medium...
Embodiment 2
[0022] 1. Inoculate the young shoots of crabapple plants on the induction medium to induce initial protocorms the size of sesame seeds; the specific composition and content of the induction medium are: KN0 3 1300mg / L, NH 4 N0 3 1200mg / L, KH 2 P0 4 120mg / L, MgS0 4 250mg / L, CaCl 2 250mg / L, KI 0.83mg / L, MnS0 4 22.3mg / L, ZnS0 4 8.6mg / L, Na 2 -EDTA 37.3mg / L, FeS0 4 27.8mg / L, sucrose 25mg / L, 6-BA 0.2mg / L, activated carbon 0.08g / L, agarose 4.5g / L, pH 5.2;
[0023] Two, the initial protocorm is transferred to the proliferation medium for proliferation culture, every four weeks, after the proliferated initial protocorm is cut, subculture is carried out, so that the protocorm proliferates rapidly, and the medium used for subculture is the same as described The proliferation medium is the same; the proliferation medium is a liquid-solid two-phase medium with improved MS as the basic medium and additional components, in which the upper layer is a liquid phase medium and t...
Embodiment 3
[0025] 1. Inoculate the young shoots of crabapple plants on the induction medium to induce initial protocorms the size of sesame seeds; the specific composition and content of the induction medium are: KN0 3 1500mg / L, NH 4 N0 3 1350mg / L, KH 2 P0 4 140mg / L, MgS0 4 300mg / L, CaCl 2 280mg / L, KI 0.83mg / L, MnS0 4 22.3mg / L, ZnS0 4 8.6mg / L, Na 2 -EDTA 37.3mg / L, FeS0 4 27.8mg / L, 30mg / L sucrose, 0.5mg / L 6-BA, 0.1g / L activated carbon, 5g / L agarose, pH 5.4;
[0026] Two, the initial protocorm is transferred to the proliferation medium for proliferation culture, every four weeks, after the proliferated initial protocorm is cut, subculture is carried out, so that the protocorm proliferates rapidly, and the medium used for subculture is the same as described The proliferation medium is the same; the proliferation medium is a liquid-solid two-phase medium with improved MS as the basic medium and additional components, in which the upper layer is a liquid phase medium and the ...
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