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PCR Reverse Blot Hybridization Assay for Screening and Identification of Pathogens in Sepsis

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Figure

TABLE 1 List of reference strains used in this study
TABLE 2 Comparison of conventional methods and PCR-REBA: screening and identification results in 120 clinical isolatesa
FIG 1 Typical PCR results for REBA Sepsis-ID test. Lanes M, 100-bp DNA ladder (Bioneer, Daejeon, South Korea); lane 1, 16S PCR (470 bp, 250 bp); lane 2,aureus S
FIG 2 Typical results of the REBA Sepsis-ID test using reference strains. All Gram-negative bacteria, Gram-positive bacteria, and fungi show strong specifichybridization signals at the positions of the corresponding probes
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