Ultralow-temperature preservation technique of callus of divaricate saposhnikovia root
A technology of cryopreservation and callus, which is applied in the field of plant tissue culture, can solve the problems that restrict the preservation of windproof germplasm resources, achieve the effect of protecting germplasm resources and reducing the economic cost of preservation
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[0025] (1) Treatment of explants: Select the full harvested parsnip seeds of the year, gently scrub with detergent water, rinse in tap water for 10 minutes, soak in clean water for 8 hours, and then transfer to 50mg / mL gibberellin Soak in solution for 10h, then soak in 75% ethanol solution for 10s in ultra-clean workbench, rinse with sterile water for 3 times, then disinfect with 0.1% mercury liter solution containing 0.01% Tween-20 for 5min, rinse with sterile water for 3 times Finally, blot the moisture on the surface with sterile filter paper for later use.
[0026] (2) Callus induction: use a sterile scalpel to cut 1 knife on the seeds treated in step (1) to create a wound, then inoculate on the induction medium for callus induction culture, and inoculate at 28°C Culture in total darkness until callus formation. The induction medium is: MS+ 4mg / L 2,4-D+ 1mg / L 6-BA+ 0.5mg / L KT+3.5% sucrose+0.5% agar+0.05% activated carbon, the pH value is 5.8.
[0027] (3) Pre-cultivation...
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