Sensitivity and specificity of polymerase chain reaction for the detection of toxoplasma gondll dna added to laboratory samples

dc.contributor.authorRachatawan Chiabchalarden_US
dc.contributor.authorชตวรรณ เฉียบฉลาดen_US
dc.contributor.authorJitbanjong Tangpong Wiengcharoenen_US
dc.contributor.authorจิตรบรรจง ตั้งปอง เวียงเจริญen_US
dc.contributor.authorYaowalark Sukthanaen_US
dc.contributor.authorเยาวลักษณ์ สุขธนะen_US
dc.contributor.otherMahidol University. Faculty of Tropical Medicine. Department of Protozoologyen_US
dc.date.accessioned2016-04-04T06:57:37Z
dc.date.accessioned2021-09-02T05:58:04Z
dc.date.available2016-04-04T06:57:37Z
dc.date.available2021-09-02T05:58:04Z
dc.date.created2016-04-04
dc.date.issued2004
dc.descriptionJoint International Tropical Medicine Meeting 2004: Ambassador Hotel, Thailand 29 November-1 December 2004: abstract. Bangkok: Faculty of Tropical Medicine, Mahidol University; 2004. p.218.en
dc.description.abstractCurrent diagnosis of Toxoplasmosis mostly relies on serological detection of specific toxoplasma immunoglobulin, mouse inoculation or tissue culture of the clinical specimens. Detection of Toxo;lasma gondii DNA using polymerase chain reaction (PCR) saves time and labors. We, therefore, studied the sensitivity and specificity of PCR to detect T.gondii DNA by aliquoting various concentration of tachyzoites in laboratory specimens from 60 positive and 10 negative buffy-coat sample containing as few as 0.25 parasites in the presence of 100,000 human leukocytes and the result was impressive with 100% specificity.en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/63423
dc.language.isoengen_US
dc.rightsMahidol Universityen_US
dc.subjectToxoplasmosisen_US
dc.titleSensitivity and specificity of polymerase chain reaction for the detection of toxoplasma gondll dna added to laboratory samplesen_US
dc.typeProceeding Posteren_US

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