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Electrophoresis biophysical

Hedrick, JL Smith, AJ, Size and Charge Isomer Separation and Estimation of Molecular Weights of Proteins by Disc Gel Electrophoresis, Archives of Biochemistry and Biophysics 126, 155, 1968. [Pg.613]

Norden, B Elvingson, C Jonsson, M Akerman, B, Microscopic Behavior of DNA Duing Electrophoresis Electrophoretic Orientation, Quarterly Reviews of Biophysics 24, 103,1991. Nozad, I Carbonell, RG Whitaker, S, Heat Conduction in Multiphase Systems—I Theory and Experiment for Two-Phase Systems, Chemical Engineering Science 40, 843, 1985. [Pg.617]

Zimm, BH Levene, SD, Problems and Prospects in the Theory of Gel Electrophoresis of DNA, Quarterly Reviews of Biophysics 25, 171, 1992. [Pg.624]

Mahmoud Hamdan and Pier Giorgio Righetti Proteomics Today Protein Assessment and Biomarkers Using Mass Spectrometry, 2D Electrophoresis, and Microarray Technology Igor A. Kaltashov and Stephen J. Eyles Mass Spectrometry in Biophysics Confirmation and Dynamics of Biomolecules... [Pg.372]

The application of high-performance capillary zone electrophoresis (HP-CZE) in its various selectivity modes has become a very valuable adjunct to HPLC for the analysis of peptides. For synthetic peptides, in particular, both HPLC and HP-CZE now form essential components of the analytical characterization of these molecules. Increasingly, zonal, micellar, or (biospecific) affinity-based HP-CZE procedures with open tubular capillary systems are adapted to allow resolution with extremely high separation efficiencies (e.g., >105 plates per meter) of synthetic or naturally occurring peptides as part of the determination of their structural, biophysical, or functional properties. Illustrative of these capabilities are the results shown in Figure 19 for the separation of several peptides with different charge and Stokes radius characteristics by HP-CZE. [Pg.609]

B. L. Karger, Y-H. Chu, and F. Foret Capillary electrophoresis of proteins and nucleic acids. Annual Review of Biophysical Biomolecular Structure 24,579(1995). [Pg.50]

Over the past two decades, capillary electrophoresis (CE) has emerged as a powerful and versatile separation tool due to its high sensitivity, resolution, and ability to detect minute quantities of samples (1-11). It is an excellent tool for many types of bioanalyses and is an unparalleled experimental tool for biophysical studies of interactions in biologically relevant media. CE differentiates charged species on the basis of mobility differences under the influence of an applied electric Held. Selectivity can be manipulated by the alteration of... [Pg.75]

D. E. Raymond, A. Manz, and H. M. Widmer, Continuous Sample Pretreatment Using A Free-Flow Electrophoresis Device Integrated Onto A Sihcon Chip, Analytical Chemistry, vol. 66, no. 18, pp. 2858-2865, Sept 1994. H. Morgan, M. P. Hughes, and N. G. Green, Separation of submicron bioparticles by dielectrophoresis, Biophysical Journal, vol. 77, no. 1, PP-516-525, July 1999. [Pg.372]

Purification of luciferase. Luciferase was isolated from the recombinant strain of Echerichia coli SL60 with lux A and B genes of Photobacterium leiognathi from the collection of the Institute of Biophysics (RAS, SB) and purified by ion-exchange chromatography.5 The purity of the luciferase according to Laemmli electrophoresis was 90-95%. [Pg.35]

Dolnik, V., DNA sequencing by capillary electrophoresis (review). Journal of Biochemical and Biophysical Methods 1999, 41,103-119. [Pg.756]


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