In-vitro regeneration culture method for downy grape
A technology of in vitro regeneration and cultivation method, which is applied in the field of agricultural science and achieves the effects of low cost, simple method and good use effect.
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Embodiment 1
[0014] Embodiment 1 of the present invention: the in vitro regeneration and cultivation method of hairy grapes, comprising the following steps,
[0015] Step 1. Establishment of the sterile line: Select the vigorously growing shoots of the "Huaxi-4" grape as explants during the growing season, rinse them under tap water, and soak them in 70% alcohol by volume for 30 seconds. Rinse with sterile water for 3 times, then immerse and disinfect with 0.1% mercury liter solution for 8 minutes, rinse with sterile water for 5 times, cut into single-bud stem segments, and inoculate them on MS medium (add 2.0 mg of per liter of MS medium) 6-benzylpurine, 0.2mg indole acetic acid, 20g sucrose and 5g agar powder, pH5.8-6.0), the temperature of MS medium is 25±1℃, and the light intensity is 40umol·s -1 m -2 , the light time is 12h / d; cultivate and induce until the axillary buds germinate, and obtain the induced axillary bud leaves;
[0016] Step 2, induction of adventitious buds: take the ...
Embodiment 2
[0019] Embodiment 2 of the present invention: the in vitro regeneration and cultivation method of hairy grapes, comprising the following steps,
[0020] Step 1. Establishment of the sterile line: Select the vigorously growing shoots of the “Nongyuan-11” grape as explants during the growing season, rinse them under tap water, and then soak them in 70% alcohol by volume for 30 seconds , washed 3 times with sterile water, then soaked and sterilized with 0.1% mercury liter solution for 8 minutes, rinsed 5 times with sterile water, cut into single-bud stem segments, and inoculated on MS medium (adding 2.0 per liter of MS medium) mg of 6-benzylpurine, 0.2 mg of indole acetic acid, 20 g of sucrose and 5 g of agar powder, pH5.8-6.0), the temperature of MS medium is 25±1°C, and the light intensity is 40umol·s -1 m -2 , the light time is 12h / d; cultivate and induce until the axillary buds germinate, and obtain the induced axillary bud leaves;
[0021] Step 2, induction of adventitious...
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