Description
| Product Name | CAT.No | Size |
| Troponin-T High Sensitivity Control | BXC0457A | 3 x 1ml |
Product Description
The Biorex Diagnostics Troponin-T High Sensitivity Control is a human serum–based, ready-to-use quality control material developed to support the accurate and reliable performance of high-sensitivity Troponin-T assays in clinical laboratories. As the detection of very low concentrations of this cardiac biomarker is essential for the early identification of myocardial injury, a dependable control is critical for verifying analytical accuracy, monitoring assay stability, and ensuring confidence in patient results. This control material is formulated to closely resemble patient samples, providing clinically relevant performance and enabling laboratories to assess method precision under routine operating conditions.
The liquid-stable format eliminates the need for reconstitution, reducing preparation time and minimising the risk of handling errors while maintaining long-term consistency between runs. Its robust design allows laboratories to identify shifts in assay calibration, detect systematic or random errors at an early stage, and maintain continuous analytical quality. By confirming the reliability of test performance across multiple batches and instruments, the control plays an important role in supporting rapid and accurate clinical decision-making for patients presenting with suspected acute coronary syndromes.
Suitable for use on major automated and semi-automated immunoassay analysers, the control integrates seamlessly into both high-throughput and routine laboratory workflows. This wide platform compatibility ensures consistent performance regardless of instrumentation, helping laboratories standardise their quality assurance procedures and achieve harmonised results.
Key Features
- Human serum–based material for optimal matrix compatibility and clinically relevant assay verification
- High-sensitivity configuration for monitoring low-level cardiac biomarker measurement
- Liquid-stable, ready-to-use format that streamlines workflow and reduces preparation variability
- Compatibility with a broad range of automated and semi-automated systems
- Supports precision and accuracy assessment across multiple runs, reagent lots, and instruments
Benefits
Routine implementation enables laboratories to maintain stringent internal quality control, ensuring dependable and reproducible results for cardiac testing. The control assists in the early detection of analytical deviations, supports method validation, and contributes to compliance with internationally recognised standards including ISO 15189, CAP, and CLIA. By strengthening assay reliability and reducing the risk of erroneous reporting, it enhances diagnostic confidence and helps clinicians make timely, informed decisions for the effective management of patients with suspected myocardial damage.
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