Ginger tissue culture method
A tissue culture, ginger technology, applied in the field of ginger tissue culture, can solve the problems of low reproduction coefficient, slow reproduction, low rooting rate and the like
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Embodiment 1
[0029] A method for rapid propagation of ginger by tissue culture, characterized in that, proceed as follows:
[0030]Pretreatment: take a ginger stem tip with a size of 0.6 cm, infiltrate it with ethanol with a volume concentration of 70% for 30 seconds, then wash it with sterile water, repeat the same ethanol infiltration once, wash it with sterile water, and heat it at 50°C 5min;
[0031] Inoculation
[0032] (1) Inoculate ginger shoot tips after pretreatment in slow-release medium and carry out primary culture, and described slow-release medium is to supplement 6-BA 0.5mg / L, NAA slow-release auxin 2mg / L in MS basal medium , TDZ 0.3mg / L, 2% sucrose, agar 0.55%, adjust the pH to 5.8;
[0033] Among them, NAA sustained-release auxin is made of nano-SiO 2 Disperse in de-ethanol ionized aqueous solution, add NAA, then add PVP k30, mix and heat to 80°C for 30 minutes, stop heating, cool to room temperature, then filter and dry to obtain SiO 2 , The mass ratio of NAA and PVP ...
Embodiment 2
[0036] A method for rapid propagation of ginger by tissue culture, characterized in that, proceed as follows:
[0037] Pretreatment: take a ginger stem tip with a size of 0.8 cm, soak it with ethanol with a volume concentration of 70% for 40 seconds, then wash it with sterile water, repeat the same soaking with ethanol once, wash it with sterile water, and heat it at 50°C 8min;
[0038] Inoculation
[0039] (1) Inoculate ginger shoot tip after pretreatment in slow-release medium and carry out primary culture, and described slow-release medium is to supplement 6-BA 1.5mg / L, NAA slow-release auxin 3mg / L in MS basal medium , TDZ 0.25mg / L, 2% sucrose, agar 0.65%, adjust the pH to 6;
[0040] Among them, NAA sustained-release auxin is made of nano-SiO 2 Disperse in de-ethanol ionized aqueous solution, add NAA, then add PVP k30, mix and heat to 90°C for 20 minutes, stop heating, cool to room temperature, then filter and dry to obtain SiO 2 , The mass ratio of NAA and PVP k30 is ...
Embodiment 3
[0043] A method for rapid propagation of ginger by tissue culture, characterized in that, proceed as follows:
[0044] Pretreatment: take a ginger stem tip with a size of 0.7 cm, soak it with ethanol with a volume concentration of 70% for 35 seconds, then wash it with sterile water, repeat the same soaking with ethanol once, wash it with sterile water, and heat it at 50°C 6min;
[0045] Inoculation
[0046] (1) Ginger stem tip after pretreatment is inoculated in slow-release medium and carries out primary culture, and described slow-release medium is to supplement 6-BA 1mg / L, NAA slow-release auxin 2.5mg / L in MS basal medium , TDZ 0.28mg / L, 2% sucrose, agar 0.6%, adjust the pH to 5.8;
[0047] Among them, NAA sustained-release auxin is made of nano-SiO 2 Disperse in de-ethanol ionized aqueous solution, add NAA, then add PVP k30, mix and heat to 85°C for 25min, stop heating, cool to room temperature, then filter and dry to obtain SiO 2 , The mass ratio of NAA and PVP k30 is...
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