Method for rapid propagation and detoxifying of stem tips of fragrant pomelo
A technology of stem tip and pomelo, applied in the field of rapid propagation and detoxification of pomelo stem tip, to avoid the influence of external factors, improve the survival rate, and improve the survival rate
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Embodiment 1
[0025] 1) Primary medium: MS medium + 0.1 mg / L NAA and / or 0.1 mg / L BA, pH 5.6.
[0026] 2) Secondary medium: MS medium + 0.1 mg / L NAA and / or 0.1 mg / L BA + 0.6 mg / L GA, pH 5.6.
[0027] 3) Basic medium: MS medium + 6-BA 0.2mg / L + NAA 0.2mg / L + sucrose 28g / L + agar 6g / L, pH 5.6.
[0028] Taking the configuration of 1L primary medium as an example, the specific preparation process is as follows: weigh the parts of MS medium required for 1L medium to dissolve and mix in sequence; then weigh NAA0.1mg and / or BA0.1mg, respectively added to MS solution to dissolve in turn, constant volume, adjust pH value to 5.6; finally subpackage, sterilize at high temperature 121℃, high pressure 0.1MPa for 15-20 minutes, cool the medium before use.
Embodiment 2
[0030] 1) Primary medium: MS medium + 0.3 mg / L NAA and / or 0.3 mg / L BA, pH 5.8.
[0031] 2) Secondary medium: MS medium + 0.3 mg / L NAA and / or 0.3 mg / L BA + 0.8 mg / L GA, pH 5.8.
[0032] 3) Basic medium: MS medium + 6-BA 0.3mg / L + NAA 0.3mg / L + sucrose 30g / L + agar 7g / L, pH 5.8.
[0033] Taking the configuration of 1L primary medium as an example, the specific preparation process is as follows: Weigh the parts of MS medium required for 1L medium to dissolve and mix in turn; then weigh NAA0.3mg and / or BA0.3mg, respectively added to MS solution to dissolve in turn, constant volume, adjust the pH value to 5.8; finally subpackage, sterilize at high temperature 121℃, high pressure 0.1MPa for 15-20 minutes, cool the culture medium before use.
Embodiment 3
[0035] 1) Primary medium: MS medium + 0.5 mg / L NAA and / or 0.5 mg / L BA, pH 6.0.
[0036] 2) Secondary medium: MS medium + 0.5 mg / L NAA and / or 0.5 mg / L BA + 1.0 mg / L GA, pH 6.0.
[0037] 3) Basic medium: MS medium + 6-BA 0.5mg / L + NAA 0.5mg / L + sucrose 32g / L + agar 8g / L, pH 6.0.
[0038] Taking the configuration of 1L primary medium as an example, the specific preparation process is as follows: Weigh the parts of MS medium required for 1L medium to dissolve and mix in sequence; then weigh NAA0.5mg and / or BA0.5mg, respectively added to MS solution to dissolve in turn, constant volume, adjust pH value to 6.0; finally subpackage, sterilize at high temperature 121℃, high pressure 0.1MPa for 15-20 minutes, cool the medium before use.
[0039] Table 1
[0040]
[0041] It can be seen from Table 1 that the choice of medium components has little effect on tissue culture.
[0042] (2) Rapid propagation and detoxification of grapefruit stem tips
[0043]A method for fast propagati...
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