CE‐SDS method development, validation, and best practice—An overview
Author:
Affiliation:
1. Kantisto BV Baarn The Netherlands
2. Faculty of PharmacyDepartment of Medicinal ChemistryUppsala University Uppsala Sweden
Publisher
Wiley
Subject
Clinical Biochemistry,Biochemistry,Analytical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/elps.201900094
Reference91 articles.
1. Kenneth S. Wätzig H. Sänger‐van de Griend C. E. Invalid rates workshop: CE‐SDS presented at CE in the Biotechnology & Pharmaceutical Industries.The 17th symposium on the practical applications for the analysis of proteins nucleotides & small molecules September 20–24 2015 Brooklyn.https://www.casss.org/page/InvalidRates.
2. Shapiro M. An FDA perspective on the implementation of state‐of‐the‐art analytical methods for the development of therapeutic proteins.Presented at WCBP Washington DC 2018.https://www.casss.org/page/SP.
3. High-performance electrophoresis: the electrophoretic counterpart of high-performance liquid chromatography
4. High-performance capillary electrophoresis of SDS-protein complexes using UV-transparent polymer networks
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