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71.
Takeishi S Rant U Fujiwara T Buchholz K Usuki T Arinaga K Takemoto K Yamaguchi Y Tornow M Fujita S Abstreiter G Yokoyama N 《The Journal of chemical physics》2004,120(12):5501-5504
DNA oligo-nucleotides, localized at Au metal electrodes in aqueous solution, are found to be released when applying a negative bias voltage to the electrode. The release was confirmed by monitoring the intensity of the fluorescence of cyanine dyes (Cy3) linked to the 5' end of the DNA. The threshold voltage of the release changes depending on the kind of linker added to the DNA 3'-terminal. The amount of released DNA depends on the duration of the voltage pulse. Using this technique, we can retain DNA at Au electrodes or Au needles, and release the desired amount of DNA at a precise location in a target. The results suggest that DNA injection into living cells is possible with this method. 相似文献
72.
Dreer S Wilhartitz P Piplits K Mayerhofer K Foisner J Hutter H 《Analytical and bioanalytical chemistry》2004,379(4):599-604
Gate oxynitride structures of TFT-LCDs were investigated by SIMS, and successful solutions are demonstrated to overcome difficulties arising due to the charging effects of the multilayer systems, the matrix effect of the method, and the small pattern sizes of the samples. Because of the excellent reproducibility achieved by applying exponential relative sensitivity functions for quantitative analysis, minor differences in the barrier gate-oxynitride composition deposited on molybdenum capped aluminium-neodymium metallisation electrodes were determined between the centre and the edge of the TFT-LCD substrates. No differences were found for molybdenum-tungsten metallisations. Furthermore, at the edge of the glass substrates, aluminium, neodymium, and molybdenum SIMS depth profiles show an exponential trend. With TEM micrographs an inhomogeneous thickness of the molybdenum capping is revealed as the source of this effect, which influences the electrical behaviour of the device.The production process was improved after these results and the aging behaviour of TFT-LCDs was investigated in order to explain the change in control voltage occurring during the lifetime of the displays. SIMS and TEM show an enrichment of neodymium at the interface to the molybdenum layer, confirming good diffusion protection of the molybdenum barrier during accelerated aging. The reason for the shift of the control voltage was finally located by semi-quantitative depth profiling of the sodium diffusion originating from the glass substrate. Molybdenum-tungsten was a much better buffer for the highly-mobile charge carriers than aluminium-neodymium. Best results were achieved with PVD silicon oxynitride as diffusion barrier and gate insulator deposited on aluminium-neodymium metallisation layers. 相似文献
73.
Fast rotation of a Bose-Einstein condensate 总被引:1,自引:0,他引:1
We study the rotation of a 87Rb Bose-Einstein condensate confined in a quadratic plus quartic potential. This trap configuration allows one to increase the rotation frequency of the gas above the trap frequency. In such a fast rotation regime we observe a dramatic change in the appearance of the quantum gas. The vortices which were easily detectable for a slower rotation become much less visible, and their surface density is well below the value expected for this rotation frequency domain. We discuss some possible tracks to account for this effect. 相似文献
74.
The lithiation pathway of 2-chloro and 2-methoxypyridine with LDA and LTMP has been investigated using deuterated probes. The availability of both H-6 and H-3 protons on the pyridine nucleus was found to be critical to ensure complete C-3 lithiation. We thus concluded that the C-3 lithiation was not a straightforward process. A mechanism involving precomplexation of lithium dialkylamides near the H-6 proton and formation of a 3,6-dilithio pyridine intermediate is proposed. 相似文献
75.
Franz Wautier Sabine Wislet-Gendebien Grazyna Chanas Bernard Rogister Pierre Leprince 《BMC neuroscience》2007,8(1):104
Background
Bone marrow stromal cells and radial glia are two stem cell types with neural phenotypic plasticity. Bone marrow mesenchymal stem cells can differentiate into osteocytes, chondrocytes and adipocytes, but can also differentiate into non-mesenchymal cell, i.e. neural cells in appropriate in vivo and in vitro experimental conditions. Likewise, radial glial cells are the progenitors of many neurons in the developing cortex, but can also generate astrocytes. Both cell types express nestin, an intermediate filament protein which is the hallmark of neural precursors. 相似文献76.
Raoul Mens Sabine Bertho Sylvain Chambon Jan D'Haen Laurence Lutsen Jean Manca Jan Gelan Dirk Vanderzande Peter Adriaensens 《Journal of polymer science. Part A, Polymer chemistry》2011,49(7):1699-1707
The optimization and control of the nanomorphology of thin films used as active layer in bulk heterojunction (BHJ) plastic solar cells is of key importance for a better understanding of the photovoltaic mechanisms and for increasing the device performances. Hereto, solid‐state NMR relaxation experiments have been evaluated to describe the film morphology of one of the “work‐horse” systems poly(2‐methoxy‐5‐(3′,7′‐dimethyloctyloxy)‐1,4‐phenylene‐vinylene)/[6, 6]‐phenyl‐C61butyric acid methyl ester (MDMO‐PPV/PCBM) in a quantitative way. Attention is focused on the influence of the processing solvent (toluene vs. chlorobenzene), the blend composition, and the casting technique, that is, spin coating versus doctor blading. It is demonstrated that independently of the solvent and casting technique, part of the PCBM becomes phase separated from the mixed phase. Whereas casting from toluene results in the development of well‐defined PCBM crystallites, casting from chlorobenzene leads to the formation of PCBM‐rich domains that contain substructures of weakly organized PCBM nanoclusters. The amount and physico‐chemical state of the phase separated PCBM is quantified by solid‐state NMR relaxation times experiments. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
77.
78.
Gerhard Friedrich Thorsten Rose Alexander Wawkuschewski Sabine Kafert-Kasting Britta Laube Lubomir Arseniev Klaus Rissler 《Chromatographia》2008,67(1-2):31-39
In a recently published paper development of a sensitive automated “on-line” solid-phase extraction (SPE)/RP-HPLC assay for
6β-hydroxytestosterone (6β-OHT) with corticosterone as the internal standard (IS) was reported and its potential for quantification
of various testosterone metabolites in culture media reflecting metabolic activity of cultured human and animal hepatocytes
demonstrated [1]. In this following contribution the technique has been extended to determination of another five testosterone metabolites
in cultured rat hepatocytes using an identical “on-line” SPE/RP-HPLC procedure and detection by tandem MS-MS with an atmospheric
pressure chemical ionization (APCI) source in the selected reaction monitoring (SRM) mode as that described in [1]. All six testosterone metabolites, namely 2α-OHT, 2β-OHT, 6α-OHT, 6β-OHT, 7α-OHT and 16α-OHT, could be sufficiently separated
from each other and thus an unequivocal assignment to the individual structures was achieved. Validation data are presented
specifying the limits of quantitation as well as the mean values of the coefficients of variation (CV) for the target analytes
and the accuracy obtained at five different days. Regio- and stereoselective testosterone hydroxylation by rat hepatocytes
was measured in a long-term culture system with and without exposure to rifampicin as an inducer of liver CYP 3A4 activity.
In addition, testosterone hydroxylation was analyzed in cultures of cryopreserved hepatocytes that had been stored at −196 °C.
The rat hepatocytes were cultured after thawing for up to 11 days and induction of testosterone hydroxylase activity could
be demonstrated in cultures which underwent a new cryopreservation protocol.
This paper is dedicated to Professor Hinrich Cramer on the occasion of his 75th birthday. 相似文献
79.
Philippe Gros Sabine Choppin Julien Mathieu Yves Fort 《The Journal of organic chemistry》2002,67(1):234-237
The determination of the initial deprotonation site of 2-chloro- and 2-methoxypyridine during reaction with BuLi-LiDMAE has been investigated. A series of experiments on deuterated regioisomers revealed a direct lithiation at C-6 excluding a potential first classical ortholithiation and lithium equilibration in the reaction medium. These results suggested that the formation of lithium aggregates at the neighboring of the pyridinic nitrogen atom favored BuLi delivery at C-6 as well as 6-lithio intermediate stabilization. 相似文献
80.