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DETECTION OF DNA-PSORALEN PHOTOADDUCTS in situ 总被引:1,自引:0,他引:1
ZOFIA ZAREBSKA† MARIA JARZABEK-CHORZELSKA ‡ GENOWEFA RZSA WIESLAW GLISKI MARIA PAWIKA TADEUSZ CHORZELSKI STEFANIA JABLOKA 《Photochemistry and photobiology》1984,39(3):307-312
Abstract— An immunological method, with the use of specific immune serum, has been developed for detection of 8-methoxypsoralen (8-MOP) photoadducts to DNA, formed in situ in cell nuclei, after combined treatment with 8MOP and UV-A irradiation (Zarçbska et al. , 1978). Lymphocytes fixed on slides or in suspension, and cryostat sections of different mammalian tissues, served as antigenic substrate, after treatment with 8-MOP and UV-A in vitro. Specific fluorescence in these substrates was detected in the nuclei after treatment with 30 ˜ 140 kJ/m2 UV-A in the presence of 0.1-0.3 μg/cm2 8-MOP. PHA-stimulated-lymphocytes appeared to be the most sensitive substrate.
However, hairless mice treated with high doses of UV-A in vivo , 70 ˜ 360 kJ/m2 did not reveal a specific fluorescence of epidermal nuclei, unless a high local concentration of 8-MOP was attained.
The apparent discrepancy in the level of photoadduct detection between the in vitro and in vivo treated specimens was explained by the low number of DNA-8-MOP-photoadducts formed in vivo under these experimental conditions. The relevance of these findings to the role of DNA-8-MOP-photoadducts formed during PUVA photochemotherapy is discussed. 相似文献
However, hairless mice treated with high doses of UV-A in vivo , 70 ˜ 360 kJ/m
The apparent discrepancy in the level of photoadduct detection between the in vitro and in vivo treated specimens was explained by the low number of DNA-8-MOP-photoadducts formed in vivo under these experimental conditions. The relevance of these findings to the role of DNA-8-MOP-photoadducts formed during PUVA photochemotherapy is discussed. 相似文献
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Vereshchagin Anatoly N. Karpenko Kirill A. Elinson Michail N. Minaeva Alexandra P. Goloveshkin Alexander S. Hansford Karl A. Egorov Mikhail P. 《Molecular diversity》2020,24(4):1327-1342
Molecular Diversity - A novel five-component diastereoselective synthesis of polysubstituted 2-piperidinones is reported. The Knoevenagel condensation–Michael addition–Mannich cascade... 相似文献
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Hendargo HC Bower BA Reinstein AS Shepherd N Tao YK Izatt JA 《Optics Communications》2011,284(19):4847-4851
Spectral domain phase microscopy (SDPM) is an extension of spectral domain optical coherence tomography (SDOCT) that exploits the extraordinary phase stability of spectrometer-based systems with common-path geometry to resolve sub-wavelength displacements within a sample volume. This technique has been implemented for high resolution axial displacement and velocity measurements in biological samples, but since axial displacement information is acquired serially along the lateral dimension, it has been unable to measure fast temporal dynamics in extended samples. Depth-Encoded SDPM (DESDPM) uses multiple sample arms with unevenly spaced common path reference reflectors to multiplex independent SDPM signals from separate lateral positions on a sample simultaneously using a single interferometer, thereby reducing the time required to detect unique optical events to the integration period of the detector. Here, we introduce DESDPM and demonstrate the ability to acquire useful phase data concurrently at two laterally separated locations in a phantom sample as well as a biological preparation of spontaneously beating chick cardiomyocytes. DESDPM may be a useful tool for imaging fast cellular phenomena such as nervous conduction velocity or contractile motion. 相似文献
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Hassan M. BortehNicholas J. Ferrell Randall T. ButlerSusan V. Olesik Derek J. Hansford 《Applied Surface Science》2011,258(1):230-235
In this work, the use of patterned proteins and peptides for the deposition of gold nanoparticles on several substrates with different surface chemistries is presented. The patterned biomolecule on the surface acts as a catalyst to precipitate gold nanoparticles from a precursor solution of HAuCl4 onto the substrate. The peptide patterning on the surfaces was accomplished by physical adsorption or covalent attachment. It was shown that by using covalent attachment with a linker molecule, the influence of the surface properties from the different substrates on the biomolecule adsorption and subsequent nanoparticle deposition could be avoided. By adjusting the reaction conditions such as pH or HAuCl4 concentration, the sizes and morphologies of deposited gold nanoparticle agglomerates could be controlled. Two biomolecules were used for this experiment, 3XFLAG peptide and bovine serum albumin (BSA). A micro-transfer molding technique was used to pattern the peptides on the substrates, in which a pre-patterned poly(dimethylsiloxane) (PDMS) mold was used to deposit a lift-off pattern of polypropylmethacrylate (PPMA) on the various substrates. The proteins were either physically adsorbed or covalently attached to the substrates, and an aqueous HAuCl4 solution was applied on the substrates with the protein micropatterns, causing the precipitation of gold nanoparticles onto the patterns. SEM, AFM, and Electron Beam Induced Current (EBIC) were used for characterization. 相似文献
5.
Eugene Kenneth Cairncross Geoffrey Spearing Hansford 《ournal of non Newtonian Fluid Mechanics》1978,3(3):203-220
Tangential and radial velocity profiles were measured for the flow about a sphere rotating slowly in a Newtonian fluid, contained in a rectangular tank. Velocities were determined from enlarged streak photographs of aluminium particles moving in a collimated “sheet” of light, at several planes through the flow field. Similar velocity profiles were measured for the flow of a 1.50% Natrosol 250 H solution about two spheres of different diameters rotating in two different sized rectangular tanks. A set of velocity distributions were also measured for a sphere rotating in a 0.9% Natrosol 250 H solution. A dye tracer study of the flow about a sphere rotating in this liquid is presented as well. Both Natrosol solutions exhibited viscoelastic behaviour. The Newtonian fluid study was carried out at a Reynolds number of 1.2 and the viscoelastic fluid studies were within the Reynolds number range of 0.05–1.24.The zero shear viscosities of the Natrosol solutions were measured using the falling-sphere method. The non-Newtonian material parameters were obtained by fitting the theoretical curves to the measured velocity data. The values of the elastic and shear thinning parameters for the two liquids obtained in the different geometrical and dynamical situations are compared. 相似文献
6.
ABSTRACT. Let G be the group ?[t, t ?1] x ?. By studying the action of the braid group Bn on the set Gn , we obtain representations of Bn into a wreath product of the symmetric group and the general linear group over ?[t, t ?1]. This in particular recovers the Burau representation of the braid group. Furthermore, some quotients of the braid group are obtained by using the representations found. 相似文献
7.
The ν5(A2u) and ν7(Eu) C–F stretching fundamentals of hexafluoroethane, C2F6, have been recorded in a supersonic jet by diode laser absorption spectroscopy. The parallel 51oband is accompanied by five satellite bands, of which three have been assigned to hot bands. A fourth satellite band arises from12CF313CF3. Transitions satisfying 0 ≤KΔK≤ 7 of the perpendicular 71oband are unperturbed while those having −10 ≤KΔK≤ 7 can be fitted assuming anRz-Coriolis interaction with a state lying at νp= 1256 cm−1. A second localized perturbation affects lines withKΔK≥ 8. The band origins are 1117.10736 (7) cm−1(51o) and 1252.96950 (17) cm−1(71o, 0 ≤KΔK≤ 7), and the rotational constantB0= 0.0615759 (27) cm−1. 相似文献
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KA Saeed FO Ayorinde BE Eribo M Gordon L Collier 《Rapid communications in mass spectrometry : RCM》1999,13(19):1951-1957
Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS) was used for the characterization of a partially transesterified poly(beta-hydroxyalkanoate), PHA, polymer produced by the bacterial strain Alcaligenes eutrophus using saponified vegetable oils as the sole carbon sources. The transesterification was carried out separately under acidic and basic conditions to obtain PHA oligomers weighing less than 10 kDa. The intact oligomers were detected in their cationized [M + Na](+) and [M + K](+) forms by MALDI-TOFMS. A composition analysis, using the MALDI-TOF spectra, indicate that the oligomers obtained via acid catalysis were terminated with a methyl 3-hydroxybutyrate end group, and those obtained by base catalysis had a methyl crotonate (olefinic) termination. In addition to HB (hydroxy butyrate), the oligomers were found to contain a small percentage of HV (hydroxy valerate). This was independently confirmed using gas chromatography/mass spectrometry (GC/MS). In comparison, the analysis of a commercial PHA polymer, transesterified under identical conditions, only showed the presence of HB, i.e. a pure PHB homopolymer. Copyright 1999 John Wiley & Sons, Ltd. 相似文献