Proliferation culture medium formula in blueberry tissue culture
A proliferation medium and tissue culture technology, applied in the field of plant tissue culture, can solve the problems of long rooting time, low reproduction coefficient, high management cost, etc., and achieve the effect of easy preparation, short time and high proliferation efficiency
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Embodiment 1
[0026] In March, take lingonberry sharpblue (the current production variety) about 15 cm from the middle and upper part of the current year's branches as explants, rinse with tap water for 15 minutes, gently scrub with gauze to remove stains, rinse with tap water for 15 minutes, and cut the rinsed branches into Small sections of 4-5cm, with 2-4 buds left for each section, put them in an ultra-clean workbench for disinfection. Disinfection procedure: 75% ethanol for 30 seconds, 0.1% mercury liter for 15 minutes (add 2-3 drops of Tween 80) and shake from time to time, then rinse with sterile water 4 times, 3 minutes each time. Cut off 0.5cm at both ends of the sterilized branches, then cut the branches into small sections of 1-2cm, keep 1-2 buds in each section, and finally inoculate the cut stem sections with buds into the pre-prepared added 0.5mg.L -1 On ordinary MS medium of ZT, culture at 25°C under 1500-2500Lex light for 2 weeks, and the light time is 12 hours / day. After 2
Embodiment 2
[0028] In March, take the middle and upper part of the lingonberry No. 3 variety (the current production variety) as explants, rinse with tap water for 15 minutes, gently scrub with gauze to remove stains, and then rinse with tap water for 15 minutes. Cut the final branches into small sections of 4-5cm, leave 2-4 buds in each section, and put them in an ultra-clean workbench for disinfection. Disinfection procedure: 75% ethanol for 30 seconds, 0.1% mercury liter for 15 minutes (add 2-3 drops of Tween 80) and shake from time to time, then rinse with sterile water 4 times, 3 minutes each time. Cut off 0.5cm at both ends of the sterilized branches, then cut the branches into small sections of 1-2cm, keep 1-2 buds in each section, and finally inoculate the cut stem sections with buds into the pre-prepared added 0.5mg.L -1 On ordinary MS medium of ZT, culture at 25°C under 1500-2500Lex light for 2 weeks, and the light time is 12 hours / day. After 2 weeks, the germinated shoots were
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