N-Glycan Analysis: Better Together
In this brochure, you will learn about Agilent solutions for sample preparation for N-glycans to support your LC/FLD/MS and CE workflows.
Development of a Rapid 2-AB Sample Preparation Workflow for N-Glycan Release and Labeling
In this application note, we will present the development and application of a rapid N-glycan sample preparation workflow using a five-minute in solution deglycosylation step followed by direct on-matrix 2-AB labeling and cleanup. Without the need for a dry down step, samples are ready for analysis in approximately 2 hours.
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Profiling Glycosylation of Monoclonal Antibodies at Three Levels Using the Agilent 6545XT AdvanceBio LC/Q-TOF
Access this application note to discover how our Q-TOF LC/MS solutions can help you in the analysis of glycoforms on the intact and reduced mAbs molecules as well as in the analysis of released glycan.
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Glycopeptide Characterization for Various Monoclonal Antibodies Using the Agilent 6545XT AdvanceBio LC/Q-TOF
In this application note, you will learn about glycopeptide analysis. This workflow shows results not only in glycan-relative quantitation, but also N-glycosylation site(s) information.
Top 10 Cleanroom Problems That Can Be Prevented via Preventative Maintenance (May 2025)
May 16th 2025Cleanrooms require strict environmental control to maintain sterility, prevent contamination, and ensure seamless operations. Without a proactive preventative maintenance (PM) program, various issues can arise, leading to costly downtime, contamination risks, and operational inefficiencies. Below are ten common cleanroom problems that can be effectively mitigated through proper PM practices.
Optimizing cGMP Facility Design Space with a Hybrid Approach (May 2025)
May 16th 2025In this webcast, we review industry drivers and risks for capital construction, with a focus on cleanroom infrastructure, and discuss the goals of using a hybrid approach while demonstrating its application and benefits using real-world examples.
Filter Sizing for Process Optimization in Life Sciences Sterile Filtration
April 24th 2025Bench-scale filterability studies play a critical role in optimizing sterile filtration in biopharmaceutical manufacturing. By guiding the selection and sizing of filters, these studies help streamline processes, improve scalability, and reduce costs. Through data-driven case studies, this paper highlights how the strategic use of pre-filters and membrane materials can maximize throughput and minimize filter fouling.