Rapid propagation method for malus halliana
A fast technology, applied in the field of rapid propagation of Begonia, can solve the problems of long cultivation time, low survival rate, and large individual differences of Begonia, and achieves short cultivation period, high survival rate, and easy to solve problems. The effect of low cutting survival rate
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Embodiment 1
[0016] A kind of rapid breeding method of crabapple, comprising the following steps:
[0017] (1) Cut off the terminal buds of 3-4-year-old robust branches, soak the cut terminal buds in alum for 10 minutes, then rinse them with clean water, dry them naturally in the shade, then soak them in hydrogen peroxide for 2 minutes, 75% medical Rinse with alcohol for 20 s, and finally rinse with double distilled water; place the terminal buds after rinsing on the primary culture medium, and after culturing for 15 days, obtain the terminal bud callus of Begonia chinensis; the primary medium is: MS As the basic medium, add 0.1 mg / L 6-benzylpurine, 0.1 mg / L zeatin, 0.5 g / L gibberellin, 0.5 mg / L ammonia water, 30 g / L glucose and 3.0 g / L agar, adjust The pH value of the induction medium was 5.8-6.2; the culture conditions were: the culture temperature was 25 °C, the light intensity was 2000 Lux, and the light time was 10 h / d.
[0018] (2) Place the callus of the top buds of Begonia chinens...
Embodiment 2
[0022] A kind of rapid breeding method of crabapple, comprising the following steps:
[0023] (1) Cut off the terminal buds of 3-4-year-old robust branches, soak the cut terminal buds in alum for 10 minutes, then rinse with clean water, dry the rinsed terminal buds naturally, and then soak them in hydrogen peroxide for 3 minutes, 75% medical use Rinse with alcohol for 20 s, and finally rinse with double distilled water; place the terminal buds after rinsing on the primary culture medium, and after culturing for 20 days, obtain the terminal bud callus of Begonia chinensis; the primary medium is: MS As the basic medium, add 2.0 mg / L 6-benzylpurine, 1.0 mg / L zeatin, 3.0 g / L gibberellin, 3.0 mg / L ammonia water, 50 g / L glucose and 5.0 g / L agar, adjust The pH value of the induction medium was 5.8-6.2; the culture conditions were as follows: the culture temperature was 30 °C, the light intensity was 3000 Lux, and the light time was 12 h / d.
[0024] (2) Place the callus of the top bu...
Embodiment 3
[0028] A kind of rapid breeding method of crabapple, comprising the following steps:
[0029] (1) Cut off the terminal buds of 3-4-year-old robust branches, soak the cut terminal buds in alum for 10 minutes, then rinse them with clean water, dry them naturally in the shade, then soak them in hydrogen peroxide for 2.5 minutes, 75% medical Rinse with alcohol for 20 s, and finally rinse with double distilled water; place the terminal buds after rinsing on the primary culture medium, and after culturing for 17 days, obtain the terminal bud callus of Begonia chinensis; the primary medium is: MS As the basic medium, add 1.0 mg / L 6-benzylpurine, 0.6 mg / L zeatin, 2.0 g / L gibberellin, 2.0 mg / L ammonia water, 40 g / L glucose and 4.0 g / L agar, adjust The pH value of the induction medium was 5.8-6.2; the culture conditions were as follows: the culture temperature was 27 °C, the light intensity was 2500 Lux, and the light time was 11 h / d.
[0030] (2) Place the callus of the top buds of Be...
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