Rapid propagation method of elaeagnus pungens
A rapid and proliferating culture medium technology, applied in the field of plants, to achieve the effect of large yield, short cycle, and large-scale planting
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Embodiment 1
[0009] Take the stalks with buds of the seeds, soak them in bleaching powder for 3 minutes, remove the surface stains with a brush, wash them with running water for 50 minutes, treat them with 75% alcohol on the ultra-clean workbench for 30 seconds, treat them with mercury chloride for 10 minutes, and rinse them with sterile water for 5-7 minutes. The formula for inserting the sterilized tuber tuber segment into the culture medium is B 5 +NAA0.1mg / L+ZT1mg / l+spermine 0.2mmol / L+10mg / L tetracycline induction medium for bud induction culture, add sucrose 30g / L, agar 6g / L, pH5.8, light 3000lx, induced The buds were put into the proliferation medium B 5 +NAA0.05mg / L+6-BA0.25mg / L+GA 3 0.1mg / L, add 30g / L sucrose, 6g / L agar, PH5.8, light 4000lx, put the clustered shoots cultured by proliferation into rooting medium B 5 +NAA0.1mg / L+3% activated carbon, the rooted test-tube seedlings of the scalloped seedlings were transplanted to the field for seedling hardening, and the survival rate...
Embodiment 2
[0011] Take the stalks with buds of the seeds, soak them in bleaching powder for 3 minutes, remove the surface stains with a brush, wash them with running water for 50 minutes, treat them with 75% alcohol on the ultra-clean workbench for 30 seconds, treat them with mercury chloride for 10 minutes, and rinse them with sterile water for 5-7 minutes. The formula for inserting the sterilized tuber tuber segment into the culture medium is B 5 +NAA0.1mg / L+ZT1mg / l+spermine 0.2mmol / L+10mg / L tetracycline induction medium for bud induction culture, add sucrose 30g / L, agar 6g / L, pH5.8, light 3000lx, induced The buds were put into the proliferation medium B 5 +NAA0.1mg / L+6-BA0.5mg / L+GA 3 0.1mg / L, add 30g / L sucrose, 6g / L agar, PH5.8, light 4000lx, put the clustered shoots cultured by proliferation into rooting medium B 5 +NAA0.3mg / L+3% activated carbon, the rooted test-tube seedlings of the scorpion mustard seedlings were transplanted to the field for hardening and cultivation, and the s...
Embodiment 3
[0013] Take the stalks with buds of the seeds, soak them in bleaching powder for 3 minutes, remove the surface stains with a brush, wash them with running water for 50 minutes, treat them with 75% alcohol on the ultra-clean workbench for 30 seconds, treat them with mercury chloride for 10 minutes, and rinse them with sterile water for 5-7 minutes. The formula for inserting the sterilized tuber tuber segment into the culture medium is B 5 +NAA0.1mg / L+ZT1mg / l+spermine 0.2mmol / L+10mg / L tetracycline induction medium for bud induction culture, add sucrose 30g / L, agar 6g / L, pH5.8, light 3000lx, induced The buds were put into the proliferation medium B 5 +NAA0.1mg / L+6-BA0.25mg / L+GA 3 0.1mg / L, add 30g / L sucrose, 6g / L agar, PH5.8, light 4000lx, put the clustered shoots cultured by proliferation into rooting medium B 5 +NAA0.1mg / L+3% activated carbon, the rooted test-tube seedlings of Sage sativa were transplanted to the field for seedling hardening, and the survival rate of S. sativa...
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