J
James W. Jorgenson
Researcher at University of North Carolina at Chapel Hill
Publications - 216
Citations - 17888
James W. Jorgenson is an academic researcher from University of North Carolina at Chapel Hill. The author has contributed to research in topics: Capillary electrophoresis & Mass spectrometry. The author has an hindex of 67, co-authored 215 publications receiving 17524 citations. Previous affiliations of James W. Jorgenson include Research Triangle Park & Indiana University.
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Automated instrumentation for comprehensive two-dimensional high-performance liquid chromatography of proteins
TL;DR: Three-dimensional (3-D) data representation provides a means of viewing peak profiles in either separation dimension and contour mapping of the 3-D data provides a more reliable means of peak identification from run to run than that provided by single-column elution times.
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Comprehensive On-Line LC/LC/MS of Proteins
TL;DR: This system uses cation-exchange chromatography followed by reversed-phase chromatography (RPLC) for the separation of protein mixtures and can be rapidly separated, desalted, and analyzed for molecular weight in less than 2 h.
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Microcolumn separations and the analysis of single cells
TL;DR: Capillary zone electrophoresis and open tubular liquid chromatography are two examples of an emerging area of analytical instrumentation known as microcolumn separations suitable for the quantitative, multicomponent chemical analysis of single cells.
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Preparation and evaluation of packed capillary liquid chromatography columns with inner diameters from 20 to 50 μm
TL;DR: Etude de l'effet du diametre de la colonne sur la performance de the colonne garnie de silice fondue modifiee par le groupement octyl as mentioned in this paper.
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Minimizing adsorption of proteins on fused silica in capillary zone electrophoresis by the addition of alkali metal salts to the buffers
TL;DR: In this paper, a method for minimizing the adsorption of proteins on fused-silica capillaries in capillary zone electrophoresis was devised, involving the use of K + concentrations of 0.3 M and above in the operating buffer.