Factory breeding method for virus-free seedlings of salviae miltiorrhizae
A technology of virus-free seedlings and salvia miltiorrhiza, applied in horticultural methods, botanical equipment and methods, gardening tools/equipment, etc., can solve problems such as unstable production of salvia miltiorrhiza and degradation of seedling vitality, and achieve prevention and control of salvia miltiorrhiza virus and well-developed root system , the effect of high detoxification rate
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Embodiment 1
[0054] 1. Materials
[0055] 1. Salvia miltiorrhiza: Triploid salvia miltiorrhiza (cultivated by the chromosome laboratory of Nankai University, Research on the cultivation and sustainable utilization of triploid salvia miltiorrhiza, Chinese Herbal Medicine, February 2012, Volume 43, No. 2, 375-379)
[0056] 2. Mercury: purchased from Shanghai Biological Engineering Co., Ltd.
[0057] 3. Initial proliferation medium: 1 / 2MS, 30g / L sugar, 6g / L agar, 0.5mg / L 6-BA, 0.2mg / L NAA, pH 5.8. Prepared by weight / volume ratio, the solvent is water. Use after routine autoclaving.
[0058] 4. Dedifferentiation proliferation medium: 1 / 2MS, 30g / L white sugar, 6g / L agar, 1mg / L 6-BA, pH 5.8. Prepared by weight / volume ratio, the solvent is water. Use after routine autoclaving.
[0059] 5. Induction medium: 1 / 2MS, 30g / L sugar, 6g / L agar, 0.2mg / L NaA, pH 5.8. The solvent is water.
[0060] 6. Root induction differentiation medium: 1 / 2MS, 30g / L white sugar, 6g / L agar, 0.5mg / L IBA, pH 5.8. Pr...
Embodiment 2
[0071] 1. Materials
[0072] 1. Salvia miltiorrhiza: triploid salvia miltiorrhiza (cultivated by the chromosome laboratory of Nankai University, (cultivated by the chromosome laboratory of Nankai University, research on the cultivation and sustainable utilization of triploid salvia miltiorrhiza), Chinese herbal medicine, February 2012, volume 43 Issue 2, 375-379))
[0073] 2. Mercury: purchased from Shanghai Biological Engineering Co., Ltd.
[0074] 3. Initial proliferation medium: 1 / 2MS, 25g / L sugar, 6g / L agar powder, 0.5mg / L 6-BA, 0.2mg / L IBA, pH 5.8. Prepared by weight / volume ratio, the solvent is water. It was filtered with a 22 μm microporous membrane and used after conventional autoclaving.
[0075] 4. Dedifferentiation proliferation medium: 1 / 2MS, 25 / L sugar, 6.5g / L agar powder, 1mg / L 6-BA, pH 5.8. Prepared by weight / volume ratio, the solvent is water. Use after routine autoclaving.
[0076] 5. Induction medium: 1 / 2MS, 25g / L sugar, 6.5g / L agar powder, 0.2mg / L IBA,...
Embodiment 3
[0087] Embodiment 3 Salvia miltiorrhiza root virus-free seedling industrialized breeding culture medium
[0088] Consists of one or more of the following media:
[0089] 1. Initial proliferation medium: 1 / 2MS, 30g / L sugar, 6.2g / L agar powder, 0.5mg / L 6-BA, 0.2mg / LNAA, pH 5.8. Prepared by weight / volume ratio, the solvent is water. Use after routine autoclaving.
[0090] 2. Dedifferentiation proliferation medium: 1 / 2MS, 30g / L sugar, 6.2g / L agar, 1mg / L 6-BA, pH 5.8. Prepared by weight / volume ratio, the solvent is water. Use after routine autoclaving.
[0091] 3. Induction medium: 1 / 2MS, 30g / L sugar, 6.2g / L agar powder, 0.2mg / L NAA, pH 5.8. The solvent is water.
[0092] 4. Root induction differentiation medium: 1 / 2MS, 30g / L white sugar, 6.2g / L agar, 0.2mg / L IBA, pH 5.8. Prepared according to weight / volume ratio, and used after filtration with 22μm microporous membrane and conventional autoclaving. The solvent is water.
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