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Comparison of the Automated Fluorescence Microscopic Viability Test With the Conventional and Flow Cytometry Methods

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dc.contributor.authorKim, Jang Su-
dc.contributor.authorNam, Myung Hyun-
dc.contributor.authorAn, Seong Soo A.-
dc.contributor.authorLim, Chae Seung-
dc.contributor.authorHur, Dae Sung-
dc.contributor.authorChung, Chanil-
dc.contributor.authorChang, Jun Koon-
dc.date.accessioned2021-09-07T21:25:00Z-
dc.date.available2021-09-07T21:25:00Z-
dc.date.created2021-06-14-
dc.date.issued2011-
dc.identifier.issn0887-8013-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/114918-
dc.description.abstractThe cell viability test is an essential tool in any laboratory, performing cell-based studies and clinical laboratory tests. The trypan blue exclusion method is the most popular assay for its simple concept among various diagnostic tools. However, several disadvantages include time-consuming and labor-intensive steps with low precision. In this study, we evaluated a new technique for the automatic cell viability measurement with microscopic cell counter and microchip. Upon blood draw from 11 healthy volunteers, Mononuclear cells were separated immediately from the heparinized whole blood, and the viable cells were diluted from 100 to 1%. The cell viability tests were performed simultaneously with following three methods: the conventional manual trypan blue exclusion method; the flow cytometry measurement with propidium iodide stain; and the newly developed microscopic cell counter with microchip. Linearities, precisions, and correlations from three methods were analyzed and compared. The correlations data from the microscopic cell counter were in good agreement with both the conventional trypan blue method (r=0.99, P<0.05) and the flow cytometry (r=0.99, P<0.05), respectively. The precision (2.0-6.2%) and linearity from the microscopic cell counter method with microchip were superior in comparison with the conventional method. The microscopic cell counter with microchip performed well with high precision, linearity, and efficient running time than both the manual trypan blue and the flow cytometry methods. J. Clin. Lab. Anal. 25:90-94, 2011. (C) 2011 Wiley-Liss, Inc.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-BLACKWELL-
dc.subjectDIACETATE PROPIDIUM IODIDE-
dc.subjectCELL VIABILITY-
dc.subjectQUANTIFICATION-
dc.subjectAPOPTOSIS-
dc.subjectCOUNTER-
dc.titleComparison of the Automated Fluorescence Microscopic Viability Test With the Conventional and Flow Cytometry Methods-
dc.typeArticle-
dc.contributor.affiliatedAuthorNam, Myung Hyun-
dc.contributor.affiliatedAuthorLim, Chae Seung-
dc.identifier.doi10.1002/jcla.20438-
dc.identifier.scopusid2-s2.0-79952667695-
dc.identifier.wosid000288397500006-
dc.identifier.bibliographicCitationJOURNAL OF CLINICAL LABORATORY ANALYSIS, v.25, no.2, pp.90 - 94-
dc.relation.isPartOfJOURNAL OF CLINICAL LABORATORY ANALYSIS-
dc.citation.titleJOURNAL OF CLINICAL LABORATORY ANALYSIS-
dc.citation.volume25-
dc.citation.number2-
dc.citation.startPage90-
dc.citation.endPage94-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMedical Laboratory Technology-
dc.relation.journalWebOfScienceCategoryMedical Laboratory Technology-
dc.subject.keywordPlusDIACETATE PROPIDIUM IODIDE-
dc.subject.keywordPlusCELL VIABILITY-
dc.subject.keywordPlusQUANTIFICATION-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusCOUNTER-
dc.subject.keywordAuthorviability-
dc.subject.keywordAuthortrypan blue-
dc.subject.keywordAuthorpropidium iodide-
dc.subject.keywordAuthorflow cytometry-
dc.subject.keywordAuthormicroscopic cell counter-
dc.subject.keywordAuthormicrochip-
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