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To establish a nucleic acid assay for detection of based on recombinase-aided isothermal amplification (RAA) assay. The gene of was selected as the target gene, and the specific primers and fluorescent probes for RAA assay were designed, screened and synthesized to establish a fluorescent RAA assay for detection of . The sensitivity of the fluorescent RAA assay was evaluated using different copy numbers of target gene sequence-contained recombinant plasmids and various concentrations of genomic DNA as templates, and the specificity of th
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