Bioprocessing Application Notes & Case Studies

  1. LC-UV-Based Synthetic Peptide Impurity Tracking And Reporting 7/29/2025

    Explore a UPLC-UV method using Empower 3 Software to assess synthetic peptide purity. Learn how integrated tools streamline impurity tracking, data reporting, and compliance in peptide analysis workflows.

  2. Characterization And Impurity Profiling Of Combined Amylin And GLP-1 Analogs 7/29/2025

    GLP-1 receptor agonists are transforming diabetes and weight loss treatment. Discover how to enable precise impurity analysis and characterization of complex, fatty acid-modified peptide therapeutics.

  3. Identification Of GLP-1 Analog Oligomeric States Using SEC-MALS 7/29/2025

    Discover how SEC-MALS enables precise characterization of GLP-1a therapeutics to ensure formulation integrity and enhance safety, efficacy, and regulatory confidence.

  4. Development Of A High Sensitivity SPE-LC-MS/MS Assay 7/29/2025

    Achieve ultra-sensitive glucagon quantification with ionKey/MS, μElution SPE, and advanced MS fragmentation to deliver low LOD, reduced sample loss, and enhanced confidence in results.

  5. Quantification Of Exenatide Using Xevo TQD 7/29/2025

    Discover a highly sensitive and reliable LC-MS/MS method for quantifying exenatide in plasma that is powered by advanced sample prep and optimized column chemistries.

  6. Application Of LC-UV/MS Workflows To Increase Efficiency 7/29/2025

    Discover how LC-UV/MS workflows help overcome analytical challenges in GLP-1 analog development to streamline impurity identification and boost lab efficiency in research.

  7. Accelerating Method Development And Manufacturing Of GLP-1 Analogs 7/29/2025

    Explore a streamlined LC-UV/MS workflow that empowers labs to meet rising GLP-1 drug demand with faster, more informed decisions that enhance compliance and impurity detection efficiency.

  8. Comprehensive Workflow For The Quantification Of Peptides And Proteins 7/29/2025

    Biologics are transforming medicine, with semaglutide leading the way. Discover how an automated LC-MS/MS workflow enables high-sensitivity quantification of peptides in plasma.

  9. Gene Therapy In-Use And Device Compatibility Studies 7/28/2025

    Discover an essential aspect of development that ensures gene therapy products remain safe, stable, and effective throughout preparation and administration by simulating real-world clinical conditions.

  10. Achieving Compliance With Confidence: The GxP Framework 7/28/2025

    Understand how to confidently meet GxP compliance in the life sciences. Explore a framework encompassing people, processes, products, and services for regulatory adherence and data integrity.