CE‐SDS method development, validation, and best practice—An overview-Reference-Cited by-同舟云学术

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

Published:2019-06-06 Issue: Volume: Page:
ISSN:0173-0835
Container-title:ELECTROPHORESIS
language:en
Short-container-title:ELECTROPHORESIS

Author:

Sänger–van de Griend Cari E.¹²^ORCID

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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