Method for detoxifying radix tetrastigme through vitrification ultralow temperature therapy
A technology of ultra-low temperature vitrification and clover, applied in horticultural methods, botany equipment and methods, plant regeneration, etc., can solve the problems of low plant tissue survival rate and low virus clearance rate, and improve the survival rate of recovery culture, damage reduction effect
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Embodiment 1
[0032] The detoxification steps of trefoil vitrification ultra-low temperature therapy are as follows:
[0033] (1) Sterile seedling cultivation: take the bud stem section with TMV cloverleaf after detection, rinse it with water, soak it with 0.1% mercuric chloride solution for 30min under aseptic conditions, then transfer it to the sodium hypochlorite solution for disinfection and disinfection Afterwards, rinse with sterile water, use sterile paper to blot the moisture on the surface of the bud stem section of A. trifoliate, and transfer it to MS medium containing 6-BA 1.0mg / L and NAA 0.5mg / L. It is 2000Lux, and the light time is 12h·d -1 , cultured at a temperature of 25±1°C for 5 days to obtain sterile seedlings of Clover.
[0034] (2) Pre-cultivation: the aseptic seedlings of A. trilobata cultivated in step (1) are 2000Lux in light intensity, and the light time is 12h·d -1 , and the temperature was 40±2°C to continue culturing for 7 days, and the medium was MS medium con...
Embodiment 2
[0039] The detoxification steps of trefoil vitrification ultra-low temperature therapy are as follows:
[0040](1) Sterile seedling cultivation: take the bud stem section with TMV cloverleaf after detection, rinse it with water, soak it with 0.1% mercuric chloride solution for 30min under aseptic conditions, then transfer it to the sodium hypochlorite solution for disinfection and disinfection Afterwards, rinse with sterile water, use sterile paper to blot the moisture on the surface of the bud stem section of A. trifoliate, and transfer it to MS medium containing 6-BA 1.0mg / L and NAA 0.5mg / L. It is 2000Lux, and the light time is 12h·d -1 , cultured at a temperature of 25±1°C for 5 days to obtain sterile seedlings of Clover.
[0041] (2) Pre-cultivation: the aseptic seedlings of the three-leaf greens cultivated in step (1) are 1800Lux in light intensity, and the light time is 13h·d -1 , and the temperature was 40±2°C for 8 days, and the culture medium was MS medium containin...
Embodiment 3
[0046] The detoxification steps of trefoil vitrification ultra-low temperature therapy are as follows:
[0047] (1) Sterile seedling cultivation: take the bud stem section with TMV cloverleaf after detection, rinse it with water, soak it with 0.1% mercuric chloride solution for 30min under aseptic conditions, then transfer it to the sodium hypochlorite solution for disinfection and disinfection Afterwards, rinse with sterile water, use sterile paper to blot the moisture on the surface of the bud stem section of A. trifoliate, and transfer it to MS medium containing 6-BA 1.0mg / L and NAA 0.5mg / L. It is 2000Lux, and the light time is 12h·d -1 , cultured at a temperature of 25±1°C for 5 days to obtain sterile seedlings of Clover.
[0048] (2) Pre-cultivation: the aseptic seedlings of A. trilobata cultivated in step (1) are 2000Lux in light intensity, and the light time is 12h·d -1 , and the temperature was 40±2°C to continue culturing for 6 days, and the medium was MS medium con...
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