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. 2011 Jan;49(1):419-22.
doi: 10.1128/JCM.01871-10. Epub 2010 Nov 17.

Novel multiplex oligonucleotide-conjugated bead suspension array for rapid identification of enterovirus 71 subgenogroups

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Novel multiplex oligonucleotide-conjugated bead suspension array for rapid identification of enterovirus 71 subgenogroups

Y Wu et al. J Clin Microbiol. 2011 Jan.

Abstract

A high-throughput multiplex bead suspension array was developed for the rapid subgenogrouping of EV71 strains, based on single nucleotide polymorphisms observed within the VP1 region with a high sensitivity as low as 1 PFU. Of 33 viral isolates and 55 clinical samples, all EV71 strains were successfully detected and correctly subgenogrouped.

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Figures

FIG. 1.
FIG. 1.
Schematic representation of the multiplex suspension array system for EV71 subgenogrouping. The VP1 region was amplified by consensus primers, and the RT-PCR product was purified by ExoSAP-IT. ASPE was performed, and only perfectly complementary strands would be amplified. The ASPE products were labeled using biotin-dCTP (black stars), and hybridized to their complementary anti-tag oligonucleotide sequences on the beads or microspheres. The complex was subjected to the Luminex reader and was identified by both lasers and streptavidin-phycoerythrin (SAPE).

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