Validation of the primerdesign quantitative allele specific amplification kit for the detection of JAK2V617F mutation

dc.contributor.authorVaz, Deborah
dc.contributor.authorNetshidzivhani, Tshiphiri
dc.contributor.authorPotgieter, Johan
dc.contributor.emaildeborah.vaz@up.ac.za
dc.date.accessioned2026-03-20T11:40:28Z
dc.date.available2026-03-20T11:40:28Z
dc.date.issued2026-03
dc.descriptionDATA AVAILABILITY STATEMENT : The data that supports the findings of this study are available in the Supporting Information of this article. Additional data may be obtained from the corresponding author upon reasonable request. The Appendix S1 provides methodological and analytical data supporting this study's findings. This includes PrimerDesign Quasa kit PCR protocols, comparative accuracy, precision, and analytical sensitivity results, WHO reference standard analyses, UK NEQAS performance data, and additional statistical analyses, including linear regression of WHO-assigned versus measured values.
dc.description.abstractINTRODUCTION : Janus Kinase 2 (JAK2) is a tyrosine kinase involved in cellular signalling. A point mutation in codon 617 of JAK2 (JAK2V617F) causes a gain-of-function effect that stimulates proliferation of myeloid cells. The aim of this study was to evaluate the Primerdesign quantitative allele-specific amplification (Quasa) kit for the detection of JAK2V617F. METHODS : Specimens previously evaluated using real-time PCR with melting curve analysis were analysed using the Quasa kit on the Bio-Rad CFX 96 platform. Results of the two PCR tests were compared to evaluate the accuracy of the kit. For intra-assay precision, samples were analysed in duplicate on the same run, and for inter-assay variation, the same known samples were tested on three non-consecutive days. The analytical sensitivity and quantitative analysis of the assay were determined using the World Health Organization (WHO) 1st International Reference Panel for Genomic JAK2V617F (United Kingdom Official Medicines Control Laboratory) and the United Kingdom National External Quality Assessment Service (UK NEQAS) results of their JAK2 p.val617phe (V617F) Mutation Status Programme. RESULTS : Concordance of the qualitative test results between the test methods was 100%. Precision experiments confirmed repeatability and reproducibility. Analytical sensitivity was confirmed at 0.1%. CONCLUSION : The PrimerDesign Quasa kit for the detection of JAK2V617F is a sensitive and reliable assay that yields reproducible qualitative results. The kit is commercially available and has, in addition, the potential for quantitative analysis when samples are analysed in duplicate. This kit assay validation may be valuable to laboratories offering or interested in offering JAK2V617F mutational testing.
dc.description.departmentHaematology
dc.description.librarianhj2026
dc.description.sdgSDG-03: Good health and well-being
dc.description.sponsorshipSupported by the Development Fund of the Department of Haematology at the University of Pretoria.
dc.description.urihttps://onlinelibrary.wiley.com/journal/10982825
dc.identifier.citationVaz, D., Netshidzivhani, T. and Potgieter, J. (2026), Validation of the Primerdesign Quantitative Allele Specific Amplification Kit for the Detection of JAK2V617F Mutation. Journal of Clinical Laboratory Analysis, 40: e70180: 1-8. https://doi.org/10.1002/jcla.70180.
dc.identifier.issn0887-8013 (print)
dc.identifier.issn1098-2825 (online)
dc.identifier.other10.1002/jcla.70180
dc.identifier.urihttp://hdl.handle.net/2263/109102
dc.language.isoen
dc.publisherWiley
dc.rights© 2026 The Author(s). Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. This is an open access article under the terms of the Creative Commons Attribution License.
dc.subjectJanus Kinase 2 (JAK2)
dc.subjectJAK2V617F
dc.subjectPolymerase chain reaction (PCR)
dc.subjectQuantitative allele specific amplification (Quasa)
dc.titleValidation of the primerdesign quantitative allele specific amplification kit for the detection of JAK2V617F mutation
dc.typeArticle

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