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Establishment of a PEG-mediated protoplast transformation system based on DNA and CRISPR/Cas9 ribonucleoprotein complexes for banana

机译:基于DNA和CRISPR / CAS9核糖核酸核糖蛋白复合物的BEG介导的原生质体转化系统的建立

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摘要

Detection of GFP fluorescence in transformed protoplasts by fluorescence microscope. pUbi-GFP plasmid was used for protoplast transformation under different transformation conditions: 40% PEG and 20 min incubation (a), 40% PEG and 30 min incubation (b), 50% PEG and 20 min incubation (c), 50% PEG and 30 min incubation (d). The protoplasts from 50% PEG with 30 min mixing were examined by flow cytometry (e). All pictures were taken after 5 days incubation in darkness. Scale bars are 75 μm
机译:荧光显微镜检测转化原生质体中的GFP荧光。在不同的转化条件下使用Pubi-GFP质粒进行原生质体变换:40%PEG和20分钟孵育(A),40%PEG和30分钟孵育(B),50%PEG和20分钟孵育(C),50%PEG 30分钟孵化(D)。通过流式细胞术(E)检查来自50%PEG的原生质体。在黑暗中孵育5天后,所有图片都是采取的。秤条是75μm

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