Tissue culturing method for chia
A technology of sage and tissue culture, applied in the field of bioengineering, can solve the problems that the tissue culture of sage has not been reported, and achieves the effects of shortening the culture time, large quantity and easy sampling.
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[0019] Example 1
[0020] Source: Salvia hispanica (salvia hispanica L) seeds as explants,
[0021] 1. Disinfection of explants and treatment of waste liquid: use Chia sage seeds as explants, disinfect by conventional methods, treat with 70% alcohol on a sterile operating table for 30 seconds, and then use 0.1% mercury Sterilize for 10-12 minutes, and finally rinse with sterile water for 5-6 times. Use a 1000ul pipette to suck out the sterilized alcohol, mercury and sterile water;
[0022] 2. Inoculation method and induction of callus and adventitious buds: The seeds of Salvia officinalis after disinfection are sucked with a 1000ul pipette and inoculated in 1 / 2MS+6-BA10.0mg / L+NAA1.0mg / L , PH 5.8 callus induction medium, inoculate 10-15 seeds per bottle in the inoculation bottle, cultivate in low light in the culture room, keep the temperature at 24±2℃; the seeds begin to germinate in about 3 days, and continue to cultivate for 12 days , Start to form callus, and at the same time d...
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[0026] Example 2
[0027] The seeds of Salvia hispanica L are explants. The basic operation method is the same as that in Example 1, but the medium for callus, adventitious bud induction and proliferation is 1 / 2MS+6-BA5.0mg / L +NAA0.5mg / L medium, the seeds begin to germinate in about 3 days, and after 15 days of continuous cultivation, callus will begin to form, and cluster buds will be differentiated at the same time. Complete plants will be formed in about 40 days, and a large number of differentiated tissue culture seedlings will be obtained after 50 days. The multiplication factor is 4~5.
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