JP/ZH: Currently, only the Luminex LTG section and the Service & Support pages regarding Luminex LTG are available in Japanese/Chinese.
A Multi-Center Clinical Evaluation of the Luminex NxTAG® Respiratory Pathogen Panel (For IVD Use) in Patients with Signs and Symptoms of Respiratory Tract Infection
Analytical Specificity Evaluation of the NxTAG® Respiratory Pathogen Panel Assay
Assessment of a High Throughput Next Generation Multiplex Respiratory Pathogen Panel
Assessment of Nasopharyngeal Swab Sample Stability for Use with Luminex NxTAG® Respiratory Pathogen Panel
Automation of Luminex® NxTAG® Respiratory Pathogen Panel (RUO)
Comparison of Luminex NxTAG Respiratory Pathogen Panel (RPP) and CLART® PneumoVir for the Diagnosis of Respiratory Pathogens in Bronchoalveolar Lavage Samples
Declaration of Conformity for NxTAG Respiratory Pathogen Panel
Detection of Influenza A H1 Subtype, Parainfluenza Viruses, Coronaviruses, Adenovirus, Enterovirus D68, Chlamydophila Pneumoniae and Mycoplasma Pneumoniae with Luminex NxTAG® Respiratory Pathogen Panel (For IVD Use) in Clinical and Contrived Specimens
Development and Validation of Fragment and Sequencing Assays as Composite Comparator Method for NxTAG® Respiratory Pathogen Panel
Development of a Semi-Quantitative Women’s Health Bacterial Panel on the Luminex® NxTAG® Platform
Environmental Monitoring and Cleaning
Evaluation of Luminex® NxTAG® Respiratory Pathogen Panel (RPP) on Nasopharyngeal Swabs
Evaluation of the Limit of Detection and Analytical Reactivity of the NxTAG® Respiratory Pathogen Panel
Evaluation of the Luminex® NxTAG® Respiratory Pathogen Panel
Evaluation of the Multi-Site Reproducibility of the NxTAG® Respiratory Pathogen Panel
Limit of Detection Study for the NxTAG® Respiratory Pathogen Panel Demonstrates Sensitivity of 102 to 104 Gene Copies/ml (EU Only)
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