CE‐SDS method development, validation, and best practice—An overview

Author:

Sänger–van de Griend Cari E.12ORCID

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

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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