Apple rootstock tissue culture rapid seedling raising method
A tissue culture and rootstock technology, applied in the field of plant tissue culture, can solve problems such as not being able to meet actual production needs, and achieve the effect of reducing production difficulty and shortening time
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Embodiment 1
[0043] Embodiment 1. Qingzhen No. 1 tissue culture rapid seedling raising method
[0044] First, the in vitro budded branches are sterilized to obtain sterile seedlings. The method is as follows: 1. Pick and cut annual robust branches with young buds during the dormant period, soak them in bromogeramine for 20 minutes, scrub the surface of the branches with a brush (especially near the buds), and then rinse them with running water. 2. Use fruit branch scissors to cut obliquely into 6-8cm stem segments in water, make sure each segment has 2-3 buds, and place them in a clean tissue culture bottle. 3. Fill a 240ml tissue culture bottle with 3 / 4 pure water, cover it tightly with a lid without a gas-permeable membrane, sterilize it in an autoclave at 125°C for 30 minutes to prepare sterile water, and cool it for later use. 4. Open the inoculator sterilizer placed in the ultra-clean workbench, insert tools such as surgical scissors, scalpels, and gun-like tweezers into the inoculat...
Embodiment 2
[0054] Embodiment two, the inventive method compares with conventional method
[0055] 1. Test materials and methods
[0056] 1.1 Materials
[0057] Green Anvil No. 1
[0058] 1.2 Test method
[0059] The conventional culture and the culture method of the present invention are adopted respectively; the method of the present invention is the method of Example 1. The general method is as follows:
[0060] Select the leaves of the explants, wash them with detergent, and rinse them under running water for about 30 minutes; then wash them with 75% alcohol and 1g·L -1 The mercuric chloride solution was disinfected for 30s and 8min, and then rinsed with sterile water for 3-5 times. Place the leaves on sterile filter paper, cut off the leaf margins and tips with a scalpel, and cut them into leaf blocks.
[0061] The culture medium and culture time used in each stage are as follows:
[0062] The basic medium is MS.
[0063] Differentiation medium: MS+5.0mg·L -1 6-BA+0.3mg·L -...
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