Method for in vitro inducing winter date anther callus
A technology for callus and callus induction, applied in horticultural methods, botany equipment and methods, plant cells, etc., can solve the problems of low callus induction rate, speed up haploid breeding process, etc., and achieve improved induction rate effect
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[0014] From May to June, immature flower buds of winter jujube with a field diameter of 0.3-0.6 cm and calyxes not yet opened were selected, and pretreated in a 4°C refrigerator for 1-3 days. Rinse with running water for 1-2 hours, put the flower buds in 70% ethanol for 30s on the ultra-clean workbench, and then transfer to 0.1% HgCl 2 In the solution for 8 minutes, rinse with sterile water for 3 to 4 times, and then peel off the anthers. When starting the culture, inoculate sterile anthers in MS+maltose 15-20g / L+TDZ 0.5-1.0mg / L +NAA 0-0.5mg / L Dark culture was carried out on the culture medium for three weeks, and then transferred to low light (800-1000 Lux) for culture. Anthers gradually produced yellow-green, loose granular callus, and gradually increased with the extension of culture time. Transfer the initial callus obtained during proliferation culture to MS+maltose 15-20g / L+TDZ 0.1-0.5mg / L +NAA 0-0.5mg / L Proliferation culture was carried out in the culture medium, a...
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