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Explore a range of resources related to our PAXgene tubes, kits and devices, including handbooks (instructions for use), brochures, technical notes and posters. View or download these documents to find out more about the full line of PAXgene products.



Link Voss, T. et al. (2021) Sensitivity assessment of workflows detecting rare circulating cell-free DNA targets: A study design proposal. PLOS ONE 16(7): e0253401 768165 References
QIAsymphony PAXgene Blood ccfDNA Kit (CE-IVD) 768566 FAQs
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Integrated Workflow for Blood Collection, ccfDNA Stabilization and Extraction for Non-Invasive Prenatal Testing (Ullius, AMP 2016) 768566 Posters
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PAXgene Blood ccfDNA Tube CE-IVD - For Stabilization of ccfDNA from Whole Blood Brochures
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PAXgene Blood ccfDNA System Transport Concept Technical Notes
Link Webinar - Considerations when generating diagnostic samples for ccfDNA analysis (March 2020) Videos and Webinars
Link Lampignano, R. et al. (2020) Multicenter Evaluation of Circulating Cell-Free DNA Extraction and Downstream Analyses for the Development of Standardized (Pre)analytical Workflows. Clin. Chem. doi: 10.1373/clinchem.2019.306837 768165 References
Link Solakoglu, Ö. et al. (2019) Characterization of circulating DNA in plasma of patients after allogeneic bone grafting. Clin. Oral Investig. [Epub ahead of print] doi: 10.1007/s00784-019-02867-3 768165 References
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Performance Comparison of PAXgene and Streck Stabilization Blood Collection Tubes for ccfDNA Testing White Papers
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Guidance Documentation for User Evaluation of Blood Collection Tubes for ccfDNA Applications White Papers
Link Zhou, R., et al. (2018) Using digital PCR to detect HER2 amplification in breast and gastric cancer patients. Frontiers Lab. Med. 2, 102. doi: 10.1016/j.flm.2018.11.002 768165 References
Link QIAsymphony PAXgene Blood ccfDNA Kit CE 768566 Safety Data Sheets
Link SDS PAXgene Blood ccfDNA Tube (CE-IVD) 768165 Safety Data Sheets
Link PAXgene Blood ccfDNA Tube (CE-IVD) IVD Handbook Handbooks
Link Zhou, R. et al. (2018) A digital PCR assay development to detect EGFR T790M mutation in NSCLC patients. Frontiers Lab. Med. 2, 89. doi: 10.1016/j.flm.2018.08.002 768165 References