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Equivalent peak resolution: Characterization of the extent of separation for two components based on their relative peak overlap.
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- Electrophoresis, 2015, v. 36, n. 5, p. 646, doi. 10.1002/elps.201400475
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Simulation of the effects of complex-formation equilibria in electrophoresis: III. Simultaneous effects of chiral selector concentration and background electrolyte pH.
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- Electrophoresis, 2012, v. 33, n. 19/20, p. 3012, doi. 10.1002/elps.201200293
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Preparative-scale isoelectric trapping by recursive electrophoresis in a compartmentalized system having orthogonal primary and secondary pH gradients. Part 2 - Operation in cascade mode.
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- Electrophoresis, 2011, v. 32, n. 20, p. 2805, doi. 10.1002/elps.201100120
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Preparative-scale isoelectric trapping by recursive electrophoresis in a compartmentalized system having orthogonal primary and secondary pH gradients. Part 1 - Construction and standard operation.
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- Electrophoresis, 2011, v. 32, n. 20, p. 2797, doi. 10.1002/elps.201100119
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Synthesis, analytical characterization and initial capillary electrophoretic use in an acidic background electrolyte of a new, single-isomer chiral resolving agent: Heptakis(2- O-sulfo-3- O-methyl-6- O-acetyl)-β-cyclodextrin.
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- Electrophoresis, 2011, v. 32, n. 19, p. 2655, doi. 10.1002/elps.201100104
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Concentration and fractionation by isoelectric trapping in a micropreparative-scale multicompartmental electrolyzer having orthogonal pH gradients. Part 2.
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- Electrophoresis, 2011, v. 32, n. 13, p. 1654, doi. 10.1002/elps.201100084
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Concentration and fractionation by isoelectric trapping in a micropreparative-scale multicompartmental electrolyzer having orthogonal pH gradients. Part 1.
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- Electrophoresis, 2011, v. 32, n. 13, p. 1647, doi. 10.1002/elps.201100083
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A systematic study in CIEF: Defining and optimizing experimental parameters critical to method reproducibility and robustness.
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- Electrophoresis, 2009, v. 30, n. 23, p. 4049, doi. 10.1002/elps.200800690
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Simulation of desalting that occurs during isoelectric trapping separations.
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- Electrophoresis, 2009, v. 30, n. 3, p. 433, doi. 10.1002/elps.200800372
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PVA-based tunable buffering membranes for isoelectric trapping separations.
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- Electrophoresis, 2008, v. 29, n. 20, p. 4247, doi. 10.1002/elps.200800180
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Determination of the operational pH value of a buffering membrane by an isoelectric trapping separation of a carrier ampholyte mixture.
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- Electrophoresis, 2008, v. 29, n. 5, p. 1077, doi. 10.1002/elps.200700698
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Synthesis of mono-6-deoxy-6- N, N, N′, N′, N′-pentamethylethylenediammonio-cyclomaltoheptaose, a single-isomer, monosubstituted, permanently dicationic β-CD and its use for enantiomer separations by CE.
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- Electrophoresis, 2007, v. 28, n. 15, p. 2589, doi. 10.1002/elps.200700028
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The Biflow: An instrument for transfer-loop mediated, continuous, preparative-scale isoelectric trapping separations.
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- Electrophoresis, 2007, v. 28, n. 13, p. 2291, doi. 10.1002/elps.200600770
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Rapid isoelectric trapping in a micropreparative-scale multicompartment electrolyzer.
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- Electrophoresis, 2007, v. 28, n. 12, p. 1851, doi. 10.1002/elps.200600846
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pH transients during salt removal in isoelectric trapping separations: A curse revisited.
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- Electrophoresis, 2007, v. 28, n. 4, p. 587, doi. 10.1002/elps.200600738
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Synthesis of a single-isomer sulfated β-cyclodextrin carrying nonidentical substituents at all of the C2, C3, and C6 positions and its use for the electrophoretic separation of enantiomers in acidic aqueous and methanolic background electrolytes, Part 4;2: Heptakis(2-O-methyl-6-O-sulfo) cyclomaltoheptaose
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- Electrophoresis, 2005, v. 26, n. 20, p. 3849, doi. 10.1002/elps.200500191
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Hydrolytically stable, diaminocarboxylic acid-based membranes buffering in the pH range from 6 to 8.5 for isoelectric trapping separations.
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- Electrophoresis, 2005, v. 26, n. 13, p. 2511, doi. 10.1002/elps.200500198
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Isoelectric buffers, part 3: Determination of pKa and pI values of diamino sulfate carrier ampholytes by indirect UV-detection capillary electrophoresis.
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- Electrophoresis, 2005, v. 26, n. 13, p. 2503, doi. 10.1002/elps.200500002
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A family of high-buffering capacity diamino sulfate isoelectric buffers for pH-biased isoelectric trapping separations.
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- Electrophoresis, 2005, v. 26, n. 1, p. 3, doi. 10.1002/elps.200406174
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High-buffering capacity, hydrolytically stable, low-p I isoelectric membranes for isoelectric trapping separations.
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- Electrophoresis, 2004, v. 25, n. 20, p. 3323, doi. 10.1002/elps.200406045
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Single-isomer sulfated α-cyclodextrins for capillary electrophoresis. Part 2. Hexakis(6-O-sulfo)-α-cyclodextrin: Synthesis, analytical characterization, and initial screening tests.
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- Electrophoresis, 2004, v. 25, n. 9, p. 1201, doi. 10.1002/elps.200405863
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Preparative-scale, recirculating, pH-biased binary isoelectric trapping separations.
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- Electrophoresis, 2004, v. 25, n. 2, p. 381, doi. 10.1002/elps.200305752
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Synthesis, analytical characterization and initial capillary electrophoretic use in acidic background electrolytes of a new, single-isomer chiral resolving agent: Hexakis(2,3-di-O-acetyl-6-O-sulfo)- α-cyclodextrin.
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- Electrophoresis, 2003, v. 24, n. 15, p. 2487, doi. 10.1002/elps.200305509
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Evolution of the theoretical description of the isoelectric focusing experiment: II. An open system isoelectric focusing experiment is a transient, bidirectional isotachophoretic experiment.
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- Electrophoresis, 2023, v. 44, n. 7/8, p. 675, doi. 10.1002/elps.202200238
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Evolution of the theoretical description of the isoelectric focusing experiment: I. The path from Svensson's steady‐state model to the current two‐stage model of isoelectric focusing.
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- Electrophoresis, 2023, v. 44, n. 7/8, p. 667, doi. 10.1002/elps.202200236
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Evolution of the theoretical description of the isoelectric focusing experiment: III. Carrier ampholyte behavior in transient, bidirectional isotachophoresis.
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- Electrophoresis, 2023, v. 44, n. 7/8, p. 689, doi. 10.1002/elps.202200239
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Front Cover.
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- Electrophoresis, 2023, v. 44, n. 7/8, p. NA, doi. 10.1002/elps.202370041
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Determination of binding constants of multiple charged cyclodextrin complexes by ACE using uncorrected and ionic strength corrected actual mobilities of the species involved.
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- Electrophoresis, 2020, v. 41, n. 7/8, p. 523, doi. 10.1002/elps.201900352
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CE determination of the thermodynamic pK<sub>a</sub> values and limiting ionic mobilities of 14 low molecular mass UV absorbing ampholytes for accurate characterization of the pH gradient in carrier ampholytes‐based IEF and its numeric simulation.
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- Electrophoresis, 2020, v. 41, n. 7/8, p. 514, doi. 10.1002/elps.201900381
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Synthesis, analytical characterization and use of octakis(2,3-di- O-methyl-6- O-sulfo)-γ-cyclodextrin, a novel, single-isomer, chiral resolving agent in low-pH background electrolytes.
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- Electrophoresis, 2003, v. 24, n. 3, p. 351, doi. 10.1002/elps.200390045
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A family of single-isomer, sulfated γ-cyclodextrin chiral resolving agents for capillary electrophoresis: Octa(6- O-sulfo)-γ-cyclodextrin.
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- Electrophoresis, 2003, v. 24, n. 1/2, p. 130, doi. 10.1002/elps.200390005
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Nonaqueous capillary electrophoretic separation of basic enantiomers using octakis(2,3- O-dimethyl-6- O-sulfo)-γ-cyclodextrin, a new, single-isomer chiral resolving agent.
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- Electrophoresis, 2002, v. 23, n. 3, p. 456, doi. 10.1002/1522-2683(200202)23:3<456::AID-ELPS456>3.0.CO;2-X
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A capillary electrophoretic system with an improved gas-phase chemiluminescence nitrogen detector.
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- Electrophoresis, 2001, v. 22, n. 17, p. 3824, doi. 10.1002/1522-2683(200109)22:17<3824::AID-ELPS3824>3.0.CO;2-5
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Heptakis(2- O-methyl-3,6-di- O-sulfo)- β-cyclodextrin: A single-isomer, 14-sulfated β-cyclodextrin for use as a chiral resolving agent in capillary electrophoresis.
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- Electrophoresis, 2001, v. 22, n. 15, p. 3152, doi. 10.1002/1522-2683(200109)22:15<3152::AID-ELPS3152>3.0.CO;2-I
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Improved preparative-scale, continuous, free-flow electrophoretic separation of the enantiomers of terbutaline utilizing equal-but-opposite enantiomer mobilities.
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- Electrophoresis, 2001, v. 22, n. 13, p. 2639, doi. 10.1002/1522-2683(200108)22:13<2639::AID-ELPS2639>3.0.CO;2-T
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Separation selectivity patterns in the capillary electrophoretic separation of anionic enantiomers by octakis-6-sulfato-γ-cyclodextrin.
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- Electrophoresis, 2001, v. 22, n. 7, p. 1394, doi. 10.1002/1522-2683(200105)22:7<1394::AID-ELPS1394>3.0.CO;2-E
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Experimental verification of a predicted, previously unseen separation selectivity pattern in the capillary electrophoretic separation of noncharged enantiomers by octakis(2,3-diacetyl-6-sulfato)-γ-cyclodextrin.
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- Electrophoresis, 2000, v. 21, n. 15, p. 3249, doi. 10.1002/1522-2683(20000901)21:15<3249::AID-ELPS3249>3.0.CO;2-C
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Experimental verification of a predicted, hitherto unseen separation selectivity pattern in the nonaqueous capillary electrophoretic separation of weak base enantiomers by octakis (2,3-diacetyl-6-sulfato)-γ-cyclodextrin.
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- Electrophoresis, 2000, v. 21, n. 10, p. 2016, doi. 10.1002/1522-2683(20000601)21:10<2016::AID-ELPS2016>3.0.CO;2-L
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Use of single-isomer, multiply charged chiral resolving agents for the continuous, preparative-scale electrophoretic separation of enantiomers based on the principle of equal-but-opposite analyte mobilities.
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- Electrophoresis, 2000, v. 21, n. 10, p. 2010, doi. 10.1002/1522-2683(20000601)21:10<2010::AID-ELPS2010>3.0.CO;2-K
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Preparative-scale isoelectric focusing separation of enantiomers using a multicompartment electrolyzer with isoelectric membranes.
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- Electrophoresis, 2000, v. 21, n. 4, p. 762, doi. 10.1002/(SICI)1522-2683(20000301)21:4<762::AID-ELPS762>3.0.CO;2-Y
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Nonaqueous capillary electrophoretic separation of basic enantiomers using heptakis(2,3-dimethyl-6-sulfato)-β-cyclodextrin.
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- Electrophoresis, 1999, v. 20, n. 13, p. 2794, doi. 10.1002/(SICI)1522-2683(19990901)20:13<2794::AID-ELPS2794>3.0.CO;2-4
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A simple method for the determination of isoelectric points of ampholytes with closely spaced pKa values using pressure-mediated capillary electrophoresis.
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- Electrophoresis, 1998, v. 19, n. 18, p. 3166, doi. 10.1002/elps.1150191819
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Capillary electrophoretic separations of enantiomers using cyclodextrin-containing background electrolytes.
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- Electrophoresis, 1997, v. 18, n. 12/13, p. 2305, doi. 10.1002/elps.1150181221
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