摘要
The use of transfer DNA (T DNA) as a mutagen has been developed for tagging genes in many crops, and results showed that T-DNA insertion is a random event, and that the inserted genes are stable through multiple generations. Through sequencing PCR-amplified fragments adjacent to the inserted elements, we can construct the T-DNA flanking database,which would be useful for cloning the genes tagged by T-DNA.
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出处
《棉花学报》
CSCD
北大核心
2002年第z1期48-,共1页
Cotton Science
