https://www.selleckchem.com/products/jph203.html
These unexpected patterns included (1) A family in which T0 transgenes and mutations were not transmitted to progeny; (2) A family with four unlinked transgene insertions, including two respectively located at paralogous CRISPR target break sites; (3) A family in which mutations were observed and transmitted, but without evidence of transgene integration nor transmission. CONCLUSIONS Genome resequencing provides high-resolution of transgene integration structures and gene editing events. Segregation patterns of these events can be compli
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