High-frequency somatic embryo regeneration culture medium capable of overcoming clover variety genotype barrier
A technology of variety genotype and regeneration medium, which is applied in the field of high-frequency somatic embryo regeneration and culture to overcome genotype barriers of clover varieties and high-frequency somatic embryo regeneration and cultivation, which can solve the problem of self-incompatibility and difficulty in solving different clover varieties and genes. It can overcome the problems of genotype barriers and the small number of varieties, so as to overcome the barriers of different varieties and genotypes, increase the frequency of regenerated plants, and achieve the effect of efficient and stable genetic transformation.
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[0073] figure 1 Embryotype cells cultured on embryogenic callus induction medium for clover explants; figure 2 It is a somatic embryo developed on the culture medium of embryo subculture for heteroclover; image 3 It is a somatic embryo developed by red clover on the embryo subculture medium; Figure 4 It is a somatic embryo developed on the culture medium of embryo subculture of Clover clover; Figure 5 Torpedo embryos developed from somatic embryos on embryo maturation and germination medium; Figure 6 Cotyledonous embryos developed from somatic embryos on embryo maturation and germination medium; Figure 7 Differentiated seedlings germinated into torpedo embryo subculture; Figure 8 Differentiated seedlings germinated into cotyledon embryo subculture; Figure 9 The seedlings developed from the differentiated seedlings of torpedo embryos; Figure 10 Seedlings developed from differentiated seedlings from cotyledon embryos.
[0074] Such as Figure 1-Figure 10 Shown: ...
Embodiment 1
[0132] A. Embryogenesis callus induction medium (improved SH+8mg / L 2,4-D+0.2mg / L 6-BA+30g / L sucrose+0.3%phytagel)+B. Embryo subculture formation medium ( Improved SH+8mg / L 2,4-D+0.2mg / L 6-BA+50g / L sucrose+0.35% phytagel)+C. Embryo maturation and germination medium (improved MS+30g / L white sugar+0.7% Agar)+D. Seedling growth acclimatization medium (1 / 2 improved MS+20g / L white sugar+0.7% agar), the pH of all above-mentioned mediums is about 5.8 after autoclaving.
Embodiment 2
[0134] A. Embryogenesis callus induction medium (improved SH+8mg / L 2,4-D+0.5mg / L 6-BA+30g / L sucrose+0.3%phytagel)+B. Embryo subculture formation medium ( Improved SH+8mg / L 2,4-D+0.5mg / L 6-BA+50g / L sucrose+0.35% phytagel)+C. Embryo maturation and germination medium (improved MS+30g / L white sugar+0.7% Agar)+D. Seedling growth acclimatization medium (1 / 2 improved MS+20g / L white sugar+0.7% agar), the pH of all above-mentioned mediums is about 5.8 after autoclaving.
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