A tissue culture method using Pan's Bingdengyulu inflorescence axis as explant
A tissue culture and ice lamp yulu technology is applied to the tissue culture of the succulent Pan's ice lamp yulu, and the tissue culture field with the inflorescence axis of Pan's ice lamp yulu as explants, so as to achieve a large value-added coefficient, improve callus induction rate, The effect of meeting production needs
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Embodiment 1
[0043] A kind of tissue culture method taking Pan's Bingdengyulu inflorescence axis as explants, it comprises the steps:
[0044] 1. Selection and disinfection of explants: At the end of March, the inflorescence rachis of Yulu in full flowering stage was selected as explants. The disinfection method was to rinse with running water for 30 minutes, then disinfect with 75% ethanol for 30 seconds on a sterile operating table, and then use 0.1% The mercuric chloride was sterilized for 8 minutes, and finally washed 6 times with sterile water for 1 minute each time, and the surface moisture was blotted with sterile paper to obtain 50 sterilized explants;
[0045] 2. Induction of callus: the detoxified explants were cut into 2.0cm long segments and inoculated in callus induction medium MS+6-BA 1.5mg / L +NAA0.3 mg / L for induction , control the culture temperature at 23°C, first cultivate in the dark for 24h, then carry out normal light culture, the light time is 10h / day, and the light i...
Embodiment 2
[0052]A kind of tissue culture method taking Pan's Bingdengyulu inflorescence axis as explants, it comprises the steps:
[0053] 1. Selection and disinfection of explants: In mid-April, the inflorescence rachis of Yulu in full flowering stage was selected as explants. The disinfection method was to rinse with running water for 30 minutes, then disinfect with 75% ethanol for 30 seconds on a sterile operating table, and then use 0.1 % mercuric chloride for 8 minutes, and finally washed 6 times with sterile water, each time for 1 minute, and blotted the surface moisture with sterile paper to obtain 50 sterilized explants;
[0054] 2. Induction of callus: the detoxified explants were cut into 2.0cm long segments and inoculated in callus induction medium MS+6-BA 1.5mg / L +NAA0.3 mg / L for induction , control the culture temperature at 27°C, first cultivate in the dark for 24h, then carry out normal light culture, the light time is 14h / day, and the light intensity is 1800lx. After 35 ...
Embodiment 3
[0061] After the explants were sterilized, they were inoculated on the induction medium containing different hormone ratios, and the effects of different medium on the callus induction rate were compared. See Table 1 for details.
[0062] Table 1 Effect of induction medium on callus induction rate
[0063]
[0064] It can be seen from Table 1 that on the MS+6-BA 1.5 mg / L +NAA0.3 mg / L medium, the explants developed best, and the callus induction rate was the highest, which was 100%.
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