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Please use this identifier to cite or link to this item: https://saber.ucv.ve/jspui/handle/10872/13285
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dc.contributor.authorPérez de Súarez, Eva-
dc.contributor.authorPérez-Schael, Irene-
dc.contributor.authorPerozo-Ruggeri, Gladys-
dc.contributor.authorde Dávila, Delia-
dc.contributor.authorRömer, Hans-
dc.contributor.authorTapia, Félix J.-
dc.date.accessioned2016-02-16T02:35:26Z-
dc.date.available2016-02-16T02:35:26Z-
dc.date.issued1987-
dc.identifier.issn1878-3503-
dc.identifier.urihttp://hdl.handle.net/10872/13285-
dc.description.abstractHuman anti-Encamoeba histolytica immunoglobulin was used to detect Entamoeba histolytica in 74 positive samples from several different sources, using an indirect immunoperoxidase method. In 73 samples, the protozoan was easily identified. Trophozoites and cysts of all cultured Entamoeba strains examined were strongly stained and as few as 3 trophozoites per microscope slide could be detected. In addition, 51 negative control samples were also tested and non-specific reactions were not observed. These pre1iminary results show that this method is both sensitive and specific, and can easily detect trophozoites and cysts of different E. histolytica strains.es_VE
dc.language.isoenes_VE
dc.publisherTransactions of the Royal Society of Tropical Medicine and Hygienees_VE
dc.relation.ispartofseriesVol. 81;Nº 4-
dc.subjectimmunoglobulines_VE
dc.subjectimmunoperoxidasees_VE
dc.subjectprotozoanes_VE
dc.subjectTrophozoiteses_VE
dc.subjectmicroscopees_VE
dc.subjectcystses_VE
dc.titleImmunocytochemical detection of Entamoeba histolyticaes_VE
dc.typeArticlees_VE
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