ROTAVIRUS DETECTION BY DOT BLOT HYBRIDIZATION ASSAY USING A NONRADIOACTIVE SYNTHETIC OLIGODEOXYNUCLEOTIDE PROBE
dc.contributor.author | FERNANDEZ, J | |
dc.contributor.author | SANDINO, A | |
dc.contributor.author | YUDELEVICH, A | |
dc.contributor.author | AVENDANO, LF | |
dc.contributor.author | VENEGAS, A | |
dc.contributor.author | HINRICHSEN, V | |
dc.contributor.author | SPENCER, E | |
dc.date.accessioned | 2025-01-23T19:22:18Z | |
dc.date.available | 2025-01-23T19:22:18Z | |
dc.date.issued | 1992 | |
dc.description.abstract | A synthetic oligodeoxynucleotide of 40 nucleotides corresponding to nucleotides 33-72 of the gene coding for the viral protein VP7 of rotavirus. was used as a nucleic acid probe to develop a non-radioactive hybridization method for rotavirus detection. The probe was labelled at the 3' end with biotin-7-dATP. The sensitivity and specificity of the dot blot hybridization assay for rotavirus detection was evaluated with 303 stool specimens. The results indicate that the hybridization assay has a higher sensitivity than both PAGE and EIA. Among the rotavirus strains tested 37 different electropherotypes were found. The results suggest that rotavirus diagnosis by dot hybridization using a non-radioactive probe may become routine laboratory procedure because it is simple, highly specific and very sensitive. | |
dc.fuente.origen | WOS | |
dc.identifier.issn | 0950-2688 | |
dc.identifier.uri | https://repositorio.uc.cl/handle/11534/99010 | |
dc.identifier.wosid | WOS:A1992HK03200018 | |
dc.issue.numero | 1 | |
dc.language.iso | en | |
dc.pagina.final | 184 | |
dc.pagina.inicio | 175 | |
dc.revista | Epidemiology and infection | |
dc.rights | acceso restringido | |
dc.subject.ods | 03 Good Health and Well-being | |
dc.subject.odspa | 03 Salud y bienestar | |
dc.title | ROTAVIRUS DETECTION BY DOT BLOT HYBRIDIZATION ASSAY USING A NONRADIOACTIVE SYNTHETIC OLIGODEOXYNUCLEOTIDE PROBE | |
dc.type | artículo | |
dc.volumen | 108 | |
sipa.index | WOS | |
sipa.trazabilidad | WOS;2025-01-12 |