Efficient inducing method of in-vitro rhizomes of Polygonatum sibiricum Red
A rhizome and in vitro technology, applied in the field of efficient induction of Polygonatum chinensis in vitro rhizomes, can solve the problems of complicated and complicated tissue culture production process of Polygonatum chinensis, unsuitable for large-scale production, contradictory market demand, etc., and achieve large-scale production application value and survival rate. High, proliferative effect
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Embodiment 1
[0025] Take the rhizomes with buds and wash them, scrub the surface with 75% ethanol, rinse with tap water, soak in 75% ethanol for 30s, rinse with sterilized deionized water twice, sterilize with 2.5% sodium hypochlorite for 5 minutes, rinse with sterilized deionized water for 2 Once again, sterilized with 2.5% sodium hypochlorite for 5 min, rinsed with deionized water for 5 times, blotted the surface moisture of the material with sterile filter paper, cut the material into bud tubers with a diameter of 0.5 cm and placed them on the adventitious bud induction medium (MS+ 6-BA1.0mg / L+2,4-D0.1mg / L+commercially available white sugar 3%+agar powder 5g / L, pH5.8~6.0), 25~27℃, light 1600Lx, light 12h / d After culturing for 35 days, 90% of the explants differentiated into adventitious buds; the tubers with differentiated adventitious buds were cut into 0.5 cm in diameter and placed in adventitious bud growth medium (MS+6-BA0.5mg / L+2,4- D0.1mg / L+ commercially available white sugar 3%+ ...
Embodiment 2
[0028] Take the rhizomes with buds and wash them, scrub the surface with 75% ethanol, rinse with tap water, soak in 75% ethanol for 30s, rinse with sterilized deionized water twice, sterilize with 2.5% sodium hypochlorite for 5 minutes, rinse with sterilized deionized water for 2 Once again, sterilized with 2.5% sodium hypochlorite for 5 min, rinsed with deionized water for 5 times, blotted the surface moisture of the material with sterile filter paper, cut the material into bud tubers with a diameter of 0.5 cm and placed them on the adventitious bud induction medium (MS+ 6-BA1.5mg / L+2,4-D0.2mg / L+commercially available white sugar 3%+agar powder 5g / L, pH5.8~6.0), 25~27℃, light 1600Lx, light 12h / d After culturing for 35 days, 90% of the explants differentiated into adventitious buds; the tubers with differentiated adventitious buds were cut into 0.5 cm in diameter and placed in adventitious bud growth medium (MS+6-BA1.0mg / L+2,4- D0.2mg / L+ commercially available white sugar 3%+ ...
Embodiment 3
[0031] Take the rhizomes with buds and wash them, scrub the surface with 75% ethanol, rinse with tap water, soak in 75% ethanol for 30s, rinse with sterilized deionized water twice, sterilize with 2.5% sodium hypochlorite for 5 minutes, rinse with sterilized deionized water for 2 Once again, sterilized with 2.5% sodium hypochlorite for 5 min, rinsed with deionized water for 5 times, blotted the surface moisture of the material with sterile filter paper, cut the material into bud tubers with a diameter of 0.5 cm and placed them on the adventitious bud induction medium (MS+ 6-BA2.0mg / L+2, 4-D0.5mg / L+commercially available white sugar 3%+agar powder 5g / L, pH5.8~6.0), 25~27℃, light 1600Lx, light 12h / d After culturing for 35 days, 90% of the explants differentiated into adventitious buds; the tubers with differentiated adventitious buds were cut into 0.5 cm in diameter and placed in adventitious bud growth medium (MS+6-BA1.5mg / L+2,4- D0.2mg / L+ commercially available white sugar 3%+...
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