Method for establishing woodbine high frequency regeneration system through somatic embryogenesis way
A high-frequency regeneration and systematic technology, applied in the field of plant cell engineering, can solve the problems of large seasonal restrictions, restrictions, and low regeneration rate of explants, and achieve the effects of normal plant development, uniform traits, and easy genetic engineering operations
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Embodiment 1
[0022] In this experiment, the seeds of N. chinensis imported from Canada were used. Soak the seeds of N. chinensis in tap water at room temperature for 10 to 15 hours, then sterilize the surface with 70% alcohol for 2 minutes, rinse them twice with sterile water, and then wash them with 0.1% Mercury Chloride (HgCl 2 ) surface sterilization for 10 minutes, rinsed with sterile water 5 times, cut out the embryos with tweezers and a scalpel and inoculated them in the culture medium containing 6-BA 2.3mg / l, 2,4-D 3.8mg / l, 600mg / l hydrolyzed milk protein Improved B 5 culture medium (Table 1). The medium contains 30g / L sucrose and 6.5g / L agar. Use 1mol / L NaOH or HCl to adjust the pH value to 5.8-6.2, sterilize with high pressure steam for 20 minutes, culture temperature at 22-28°C, light-dark cycle 16h / 8h, light intensity 2000-25001x, relative humidity 60%-70%. 30 days to replace the fresh medium.
[0023] The callus began to appear in 10-12 days, and the callus grew rapidly aft...
Embodiment 2
[0030] The culture procedures were all carried out according to Example 1, except that in the first stage, 1.1mg / l 6-BA, 2.2mg / l 2,4-D and 400mg / l hydrolyzed milk protein LH were added to the culture medium, and in the second stage 0.9mg / l 2,4-D and 0.45mg / l 6-BA were added to the first subculture medium, and 0.5mg / l 2,4-D and 0.25mg / l 6-BA were added to the second subculture medium. l 6-BA, supplemented with 0.5mg / l 2,4-D and 0.25mg / l 6-BA in the third subculture medium, the embryogenic callus obtained by subculture in the third stage was transferred to Growth regulator, supplemented with 600mg / l hydrolyzed milk protein B 5 performed on culture medium.
Embodiment 3
[0032] The culture procedures were all carried out according to Example 1, except that in the first stage, 1.3mg / l 6-BA, 1.9mg / l 2,4-D and 500mg / l hydrolyzed milk protein LH were added to the medium, and in the second stage Add 1.25mg / l 2,4-D and 0.65mg / l 6-BA to the first subculture medium, add 0.65mg / l 2,4-D and 0.35mg / l to the second subculture medium 6-BA, 0.65mg / l 2, 4-D and 0.35mg / l 6-BA were added to the third subculture medium, and the embryogenic callus obtained by subculture was transferred to no growth medium in the third stage. Regulator, B with additional 580 mg / l hydrolyzed milk protein 5 performed on culture medium.
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