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 to 5.8-6.2, sterilize with high pressure steam for 20 minutes, cultivate at 22-28°C, light-dark cycle 16h / 8h, light intensity 2000-2500lx, 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 after 18 days. In ...
Embodiment 2
[0030] The culture procedures were all carried out as in Example 1, except that the first stage added 6-BA 1.1 mg / l, 2,4-D 2.2 mg / l and LH 400 mg / l (the same below), and the second stage The first passage was 2,4-D0.9mg / l, 6-BA was 0.45mg / l, the second passage was 2,4-D0.5mg / l, 6-BA was 0.25mg / l, the third The second subculture is 2,4-D0.5mg / l, 6-BA is 0.25mg / l, and the third stage is to transfer the embryogenic callus obtained by subculture to no growth regulator, add 400mg / l hydrolyzed milk protein modification B 5 performed on culture medium.
Embodiment 3
[0032] The culture procedures were all carried out according to Example 1, except that the first stage added 6-BA1.3mg / l, 2,4-D 1.9mg / l and 500mg / l (units the same below), and the second stage The first passage was 2,4-D1.25mg / l, 6-BA was 0.65mg / l, the second passage was 2,4-D0.65mg / l, 6-BA was .035mg / l, the third The subculture is 2,4-D0.65mg / l, 6-BA is 0.35mg / l, in the third stage, the embryogenic callus obtained by subculture is transferred to no growth regulator, and 460mg / l hydrolyzed milk protein is added the B 5 performed on culture medium.
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