As your partner in clinical testing, we understand the impact of your accuracy and speed on decisions made by healthcare professionals, researchers, and scientists. That’s why our unparalleled portfolio of analytical solutions is backed by guaranteed quality and reliable delivery. Our application-optimized reagents, reference materials, and tools empower every stage of your workflow. And our team supports you with expert technical assistance, for example to design and run lab developed tests (LDTs) for clinical diagnostics. Whether you’re performing LC-MS, PCR, or ELISA testing methods, we’ll help you raise your precision, so that healthcare professionals can trust their decisions.
Select your preferred diagnostic method to review its workflow and directly purchase analytical products.
LC-MS is a powerful analytical technique used more and more in clinical laboratories to analyze complex mixtures and identify and quantify various substances, such as drugs, metabolites, and biomarkers, in patient samples. It offers, often in combination with distinct and robust sample preparation techniques -depending on sample and analyte type, high sensitivity, selectivity, allowing for accurate and fast results for targeted determinations and screenings. LC-MS is particularly valuable in detecting low concentrations of analytes and in identifying unknown compounds, making it an essential tool for enhancing patient care and improving treatment outcomes in today's clinical labs in hospitals. Fundament for reliable results are suitable standards such as certified reference materials to ensure accurate identifications and quantifications.
Effective sample prep is critical to accurate and efficient analysis. Improve your analysis and protect your instrument by concentrating and purifying your sample
Reference materials are a critical component of analytical testing workflows and broader quality assurance schemes. Qualify and calibrate your instruments and assays.
Columns, solvents, reagents and accessories have a critical impact on the accuracy, reliability and efficiency of your analysis. Leverage the available technical resources to optimize your approach.
PCR testing is used to analyze the presence, length, or sequence of DNA or RNA. The PCR workflow starts with sample collection, followed by sample preparation, and concludes with DNA/RNA target-specific amplification. Typically, the post-amplification analysis is performed via qPCR in which quantification is performed in real time during the amplification cycles. An alternative is end-point PCR in which results are determined after the amplification cycles have been completed. A key goal in preparing a DNA or RNA library for next generation sequencing is to maximize complexity while reducing PCR or other amplification-introduced biases, as the quality of the resulting library can strongly impact NGS results.
Enzyme-linked immunosorbent assay (ELISA) is an immunoassay technique widely used for high-throughput screening and quantification of antibodies, proteins, peptides, and other small molecules. ELISAs are typically run on a 96-well plate format. Plates can be supplied ready to use for in vitro diagnostics (IVDs) or prepared in-house for lab-developed tests (LDTs).
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