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Restriction Enzyme Pattern Analysis of Mycobacteria DNA by Capillary Electrophoresis with Laser-Induced Fluorescence Detection
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A new method for rapidly detecting restriction enzyme patterns of Mycobacterium DNA using capillary electrophoresis with laser-induced fluorescence detection (CE-LIFD) was developed.
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The UV-vis absorption and fluorescence spectra, thermal stability of spectral property, phase transition behavior and morphology of the synthesized polymers were investigated.
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With increasing the length of the alkyl side chain, the UV and fluorescence spectra exhibit an obvious blue shift compared with those of the unsubstituted polymer.
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The effective segregation coefficients of W and Sr elements in SrWO4 single crystal are close to 1 by the X-ray fluorescence method.
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Thiols were converted to fluorescent derivatives by precolumn derivatization with monobromobimane.
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The scavenging effect of compounds on hydroxy radicals was detected by fluorescent spectrophotometry.
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QDs were embedded in the polymer beads with the specific functional groups through dissolving and swelling method, which provided the condition for the conjunction of biomolecules and QDs as fluorescent probes.
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A study of using luminophore-doped silica nanoparticles as fluorescent probe in protein microarray assay
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These nanoparticles were further used as fluorescent probes in protein microarray assay for the quantitative detection of protein.
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X-ray diffraction (XRD) was applied to get the parameters of the LBO structure, thermoluminescence (TL) and optically stimulated luminescence (OSL) were measured, and a second-order exponential decay model was fitted to the OSL decay curves.
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The luminescent properties of the samples were investigated and the up-conversion luminescence of Er3+, Ho3+ and Tm3+ doped Sr2CeO4 phosphors was observed.
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Their fluorescence properties were studied by photoluminescence, which indicated that the luminescence wavelength of 5-and 2-substitued-8-hydroxyquinoline derivatives shifted to red in comparison with that of 8-hydroxyquinoline.
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The sensitivity of the luminescence of the strains to certain toxic agents has been compared to that of the test strain Ph.
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Effect of Antibacterial Factors and Biostimulators of Cell Metabolism on Bacterial Luminescence
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The fluorescence properties of the solid complexes and their solutions were investigated in detail.
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The results indicated that the weak election-withdrawing group 4-hydroxymethyl in 4-position of pyridine in 4-HMDPA could weaken the fluorescence intensity of the lanthanide complexes.
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Meanwhile, the fluorescence lifetime of 2-[2-(9-ethyl-9H-carbazol-2yl)-vinyl]-quinolin-8-ol and its zinc complex showed long lifetime in benzene solution.
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In accordance with the fluorescence intensity of organic cell walls, two groups of microfossils were distinguished.
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The DsRed absorbance and circular dichroism spectra revealed that the fluorescence loss was accompanied by protein denaturation.
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