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The polymerase chain reaction (PCR), a sensitive tool for the identificationof specific regions of DNA present in small quantities, was used to detect the presence of T-DNA in 34 Agrobacterium strains from Vitis spp. Oligonucleotide primers, homologous to T-DNA regions from a wide and a narrow host range strain of Agrobacterium tumefaciens, were used to amplify portions of the T-DNA. In most cases the PCR results confirmed pathogenicity tests using detached leaves from Agrobacterium-free muscadine plants and DNA slot blot hybridization (...)
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Lu Dong (1992) studied this question.
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