Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/9523
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dc.contributor.authorJenkins, Margaret Aen
dc.contributor.authorRatnaike, Sujivaen
dc.date.accessioned2015-05-15T22:38:52Z
dc.date.available2015-05-15T22:38:52Z
dc.date.issued2003-06-01en
dc.identifier.citationClinical Chemistry and Laboratory Medicine; 41(6): 747-54en
dc.identifier.govdoc12880137en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/9523en
dc.description.abstractCapillary electrophoresis (CE) has been used in a variety of in-house capillary isoelectric focusing (CIEF) and capillary zone electrophoresis (CZE) assays for the detection of hemoglobin (Hb) variants and the quantitation of HbA2 and HbF. A commercial kit has also been produced for the analysis of hemoglobin variants and thalassemia screening. Though CE methods have been shown to be able to detect many variants, final identification of the variant needs specialized testing such as DNA technology. Over the past 2 years, many instruments that had been used for these hemoglobin variant screening and thalassemia assays have been withdrawn from sale. Although CE HbA1c analysis is available, it cannot compete in turnaround time or cost with automated HPLC commercial instruments that give accurate HbA1c results in 3 or 4 minutes. Hence we do not anticipate a bright future for the analysis of hemoglobin by CE.en
dc.language.isoenen
dc.subject.otherChromatography, High Pressure Liquiden
dc.subject.otherElectrophoresis, Capillary.methodsen
dc.subject.otherFetal Hemoglobin.analysisen
dc.subject.otherHemoglobin A2.analysisen
dc.subject.otherHemoglobins.analysis.classificationen
dc.subject.otherHumansen
dc.subject.otherIsoelectric Focusing.methodsen
dc.subject.otherThalassemia.complicationsen
dc.subject.otherTime Factorsen
dc.titleCapillary electrophoresis of hemoglobin.en
dc.typeJournal Articleen
dc.identifier.journaltitleClinical chemistry and laboratory medicine : CCLM / FESCCen
dc.identifier.affiliationDivision of Laboratory Medicine, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.doi10.1515/CCLM.2003.114en
dc.description.pages747-54en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/12880137en
dc.type.austinJournal Articleen
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
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