Novel method for tissue culture rapid propagation of acer paimatum
A technology of the Acer palmatum group and a new method, which is applied in the biological field, can solve the problems of low cutting propagation coefficient, unfavorable industrial production, and increased production costs, and achieve the effects of shortening the propagation time, convenient operation, and low cost
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Embodiment 1
[0018] Example 1: A method for tissue culture and rapid propagation of Acer with chicken feet, which comprises the following steps:
[0019] S1. explant explants: collect disease-free young stems of Acer, cut into 2cm-long stems, rinse in running water for 5 minutes, and absorb water;
[0020] S2. Sterilization: put the rinsed explants into the ultra-clean workbench, disinfect with 70% alcohol for 13s, rinse with sterile water for 4 times, and then put them into 0.1% mercuric chloride for sterilization 5min, rinse 4 times with sterile water, and place on sterile paper to dry;
[0021] S3. Start-up culture: inoculate the sterilized explants in a start-up medium for culture, wherein the start-up medium is WPM+GA 3 0.1mg / L+TDZ 0.05 mg / L+sucrose 30g / L+agar 5g / L, pH 5.5, culture conditions: light intensity 2800LX, light time 14h, temperature 23°C, culture time 14d, axillary bud elongation after initiation of culture 2cm;
[0022] S4. Rooting culture: choose the stem segment o...
Embodiment 2
[0023] Example 2: A method for tissue culture and rapid propagation of Acer with chicken feet, which comprises the following steps:
[0024] S1. Cut out explants: collect disease-free young stems of Acer chinensis, cut them into 3 cm long stems, rinse in running water for 10 minutes, and absorb water;
[0025] S2. Sterilization: put the rinsed explants into the ultra-clean workbench, disinfect with 75% alcohol for 18s, rinse with sterile water for 6 times, and then put them into 0.2% mercuric chloride for sterilization 10min, rinse with sterile water 6 times, and place on sterile paper to dry;
[0026] S3. Start-up culture: inoculate the sterilized explants in a start-up medium for culture, wherein the start-up medium is WPM+GA 3 0.1mg / L+TDZ 0.05mg / L+sucrose 30g / L+agar 5g / L, pH 6.5, culture conditions: light intensity 3200LX, light time 18h, temperature 25°C, culture time 21d, axillary bud elongation after initiation of culture 4cm;
[0027] S4. Rooting culture: choose t...
Embodiment 3
[0028] Example 3: A method for tissue culture and rapid propagation of Acer with chicken feet, which comprises the following steps:
[0029] S1. Cut out explants: collect disease-free young stems of Acer, cut into 2.5cm-long stems, rinse in running water for 8 minutes, and absorb water;
[0030] S2. Sterilization: put the rinsed explants into the ultra-clean workbench, disinfect with 73% alcohol for 15s, rinse with sterile water for 5 times, and then put them into 0.2% mercuric chloride for sterilization 8min, rinse with sterile water 5 times, and place on sterile paper to dry;
[0031] S3. Start-up culture: inoculate the sterilized explants in a start-up medium for culture, wherein the start-up medium is WPM+GA 3 0.1mg / L+TDZ 0.05mg / L+sucrose 30g / L+agar 5g / L, pH 5.5~6.5, culture conditions: light intensity 3000LX, light time 15h, temperature 24°C, culture time 18d, after starting the culture, axillary buds Elongate 3cm;
[0032] S4. Rooting culture: select the stem segme...
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