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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Embodiment 1
[0020] Materials: chia sage (salvia hispanica L) seeds as explants,
[0021] 1. Disinfection of explants and waste liquid treatment: choose chia seeds as explants, disinfect them with conventional methods, treat them with 70% alcohol for 30 seconds on a sterile operating table, and then use 0.1% mercuric chloride Disinfect for 10-12 minutes, and finally rinse with sterile water for 5-6 times, and suck out the disinfected alcohol, mercury chloride water and sterile water with a 1000ul pipette;
[0022] 2. Inoculation method and induction of callus and adventitious buds: Sterilized chia seeds were sucked with a 1000ul pipette gun and inoculated in 1 / 2MS+6-BA10.0mg / L+NAA1.0mg / L , on the callus induction medium with a pH value of 5.8, inoculate 10-15 seeds per bottle in the inoculation bottle, culture in the culture room with low light, and keep the temperature at 24±2°C; the seeds start to germinate in about 3 days, and continue to culture for 12 days , began to form callus, and...
Embodiment 2
[0027] Chia sage (salvia hispanica L) seeds are explants, and the basic operation method is consistent with Example 1, but its callus, adventitious bud induction and proliferation medium are 1 / 2MS+6-BA5.0mg / L +NAA0.5mg / L medium, the seeds began to germinate in about 3 days, and after 15 days of continuous culture, callus tissue began to form, and at the same time clustered buds were differentiated, and a complete plant was formed in about 40 days, and a large number of differentiated tissue culture seedlings were obtained after 50 days. The multiplication factor is 4-5.
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