## Abstract A lampβbased fluorescence detection (Flu) system for CE was extended with a wavelengthβresolved (WR) detector to allow recording of full protein emission spectra. WRFlu was achieved using a fluorescence cell that employs optical fibres to lead excitation light from a XeβHg lamp to the c
Time- and Wavelength-Resolved Fluorescence Detection for Capillary Zone Electrophoresis with Axial Excitation
β Scribed by Angela Fultz; Todd M. Branch; Vahid Majidi
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 210 KB
- Volume
- 57
- Category
- Article
- ISSN
- 0026-265X
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β¦ Synopsis
Capillary zone electrophoresis (CZE) has become a powerful tool in separation science. Detection methods for this technique, however, have not yet matured. We describe here two axial optical detection methods with time and wavelength resolution for CZE. CZE separation of rhodamine dyes was carried out in a 200-mm capillary. A 100-mm fiberoptic cable was inserted into the capillary to the edge of the observation window. The fiberoptic was used to transmit laser radiation, which served as the excitation source for fluorescence spectroscopy. Separation of rhodamine 590 from rhodamine 610 and kiton red was achieved. Time-resolved detection allowed the analysis of protein-rhodamine B isothiocyanate conjugates as well as detection of the sensitized fluorescence of fluorescein in the presence of coumarin.
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## Abstract CIEF and CZE are coupled with LIF detection to create an ultrasensitive 2βD separation method for proteins. In this method, two capillaries are joined through a bufferβfilled interface. Separate power supplies control the potential at the injection end of the first capillary and at the
Capillary zone electrophoresis (CZE) was applied to the characterization of highly polar marine toxins that can be difficult to address using traditional chromatographic methods. Separation efficiencies of nearly 400,000 theoretical plates were obtained in just over 10 min. Laser fluorescence detect
A capillary electrophoretic (CE) method is presented for the determination of the collagen crosslinks hydroxylysylpyridinoline (HP) and lysylpyridinoline (LP). Various detection techniques are compared, i.e. UV-Vis diode-array absorbance detection (DAD) and fluorescence detection both in the laser-i