Featured Resources
43:00
Harnessing Novel MS Approaches (MAM, IEX-MS) to Accelerate Biotherapeutic Development and Analysis

MAM workflows are implemented differently according to the vagaries of your organisation. Ben Niu speaks to the Astra implementation across product and process characterization to optimise throughput whilst respecting robustness and variability .

56:09
Intact Antibody and Plasma Glycoprotein Analysis with Native MS

Albert Heck talks about how Native MS can provide detailed information about the structural integrity, glycosylation patterns, drug loading and non-covalent interactions of mAbs and other biopharmaceuticals.

20:15
Automated Feedback Control of Protein Characteristics in a Perfusion Bioprocess

“Open-loop control” is standard control strategy for biomanufacturing – Critical Quality Attributes (CQAs) are maintained within set ranges by controlling Critical Process Parameters (CPPs). Mass spectrometry is an ideal tool for PAT.

33:28
質量分析によるオリゴヌクレオチド分析:配列の表示および自動化はもはやシーシュポスの作業(果てしない徒労)ではない

For fast ranking during expression vector design and clone selection, Lonza's setup for high throughput intact MS uses Protein Metric’s parsimonious charge deconvolution algorithm.

38:23
Tackling the Glycan Isomer Challenge for your Biotherapeutics

As minor changes to production processes can influence both glycan structure and composition, glycans must be monitored. However, characterization of N-linked glycosylation is analytically challenging due to innate glycan microheterogeneity.

23:18
EU UGM 2023: Protein Metrics’ MAM application as a robust standard for PTM detection in large scale forced degradation studies

Creating robust standards and high throughput method development for large scale forced degradation studies and PTM reporting

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