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Enhancing the characterization of mRNA lipid nanoparticle drugs and vaccines with new LC-MS solutions
Discover how a quadrupole time-of-flight (QTOF) system can be used for high-resolution quantitation of oligonucleotides.
Achieve better productivity in your elemental analysis: Switch from Flame Atomic Absorption (AAS) to MPAES
The technology and the applications that can be easily resolved by MP-AES.
ASB/OSAC Compliance Testing – One Box, One Analyst, One Instrument
Learn how to implement lean principles into your lab: ASB/OSAC Compliance Testing – One Box, One Analyst, One Instrument
Determination of Optical Properties of Advanced Materials through Angular UV-Vis-NIR Measurements
How angular measurements can be made through the use of a Cary 7000 and its UMA (Universal Measurement Accessory).
Simplified Workflows for Glycan Analysis Combining Speed, Simplicity, and Unrivaled Sensitivity
Current challenges faced with glycan analysis, learn how to develop comprehensive workflow-based solutions.
LC-MS/MS Analysis of Serum Estrogens for Clinical Research
The aim of this presentation is to demonstrate the performance of the ACQUITY UPLC™ I-Class and Xevo™ TQ-Absolute for the quantification of estrogens for clinical research.
The Impact of Reliable Automation in Translational Metabolomics
How automated liquid handling for LC-MS/MS sample preparation contributed to the identification and quantification of over 30 metabolites.
Empower LMS Inventories
In this session we show you how you streamline your documentation and replace paper by electronic recording
Enhance performance with innovative GC Supplies
Join us in this webinar focused on GC supplies specially designed to improve ease-of-use and enhance analytical results, instrument performance and laboratory efficiency.
Which system do I need for dioxin analysis: GC magnetic Sector, GC-MS/MS or GC Orbitrap MS?
Join us for a webinar where our applications specialists will discuss the theory with real-world data. Examples will be given to highlight the advantages of each technique in meeting regulatory criteria.
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