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dc.contributor.authorEryilmaz, E
dc.contributor.authorYillar, Gaye
dc.contributor.authorDeniz, G
dc.contributor.authorYanikkaya-Demirel, G
dc.contributor.authorKuzu-Karsilayan, H
dc.date.accessioned2021-03-03T19:54:34Z
dc.date.available2021-03-03T19:54:34Z
dc.date.issued2002
dc.identifier.citationKuzu-Karsilayan H., Eryilmaz E., Yillar G., Deniz G., Yanikkaya-Demirel G., "Spectrophotometric determination of leukocytes in blood", JOURNAL OF CLINICAL LABORATORY ANALYSIS, cilt.16, sa.5, ss.233-236, 2002
dc.identifier.issn0887-8013
dc.identifier.otherav_5704a023-01d6-4638-b843-3b59f16b44e4
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/61407
dc.identifier.urihttps://doi.org/10.1002/jcla.10049
dc.description.abstractThe determination of leukocyte concentration in human blood depending on the detection of oxidized o-dianisidine in acidic solution is studied. The oxidation of o-dianisidine was carried out by peroxidase enzymes found in leukocytes. The reaction was stopped by the addition of 4N H2SO4 to the solution, and a very stable, colored o-dianisidine derivative was obtained. The calibration graph was plotted with the recorded absorbance values at 400 nm assigned to the y-axis, and leukocyte counts in 1-mL blood samples to the x-axis. The equation of the calibration graph was y=0.0025x+0.0904, with a correlation coefficient of R=0.994. The coefficient of variation and P-value of the method were 4.00% and 0.05%, respectively. (C) 2002 Wiley-Liss, Inc.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.subjectTIBBİ LABORATUVAR TEKNOLOJİSİ
dc.subjectKlinik Tıp
dc.subjectTıp
dc.titleSpectrophotometric determination of leukocytes in blood
dc.typeMakale
dc.relation.journalJOURNAL OF CLINICAL LABORATORY ANALYSIS
dc.contributor.department, ,
dc.identifier.volume16
dc.identifier.issue5
dc.identifier.startpage233
dc.identifier.endpage236
dc.contributor.firstauthorID164184


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