A kind of tissue culture method of North American holly
A technology of tissue culture and holly, applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of low reproduction coefficient and achieve the effects of high survival rate, pure quality, and strong branches
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Embodiment 1
[0023] On the morning of June 13, 2012, healthy and typical ornamental plants were selected from the female seedlings of North American holly, and the semi-lignified branches of the year were collected. Cut off the leaves after collection, while retaining the 1.2cm petiole, rinse with tap water, soak in detergent solution for 6 minutes, and then rinse with tap water for 1 hour for later use; on the ultra-clean workbench, cut the cleaned branches into 2.5cm single Buds and stems are disinfected sequentially, soaked in 75% alcohol solution for 30 seconds, rinsed with sterile water for 5 times, soaked in 1‰ mercury liter solution for 6 minutes, and shaken continuously to make the disinfection complete, and finally rinsed with sterile water for 8 times; then Use a sterile knife to cut off the 0.2cm dead tissue at the upper and lower ends of the stem segment, and insert the treated stem segment plant morphological lower end into the prepared induction differentiation medium: the for...
Embodiment 2
[0029] On the morning of May 14, 2013, healthy and typical ornamental plants were selected from the female seedlings of North American holly, and the semi-lignified branches of the year were collected. Cut off the leaves after collection, while retaining the 1.0cm petiole, rinse with tap water, soak in detergent solution for 8 minutes, and then rinse with tap water for 1 hour for later use; on the ultra-clean workbench, cut the cleaned branches into 2.2cm single buds The stems are soaked in 75% alcohol solution for 30s in turn, after pouring off the alcohol, rinse with sterile water for 5 times, then add 1‰ mercury liter solution to soak for 6 minutes, shake continuously during this period, pour out the mercury liter solution and rinse with sterile water 8 times for standby; then use a sterile knife to cut off the 0.25cm dead tissue at the upper and lower ends of the stem segment, and insert the lower end of the stem segment plant morphology into the prepared differentiation in...
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