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排序方式: 共有84条查询结果,搜索用时 15 毫秒
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W. S. Holland P. A. R. Ade M. J. Griffin I. D. Hepburn D. G. Vickers C. R. Cunningham P. R. Hastings W. K. Gear W. D. Duncan T. E. C. Baillie E. E. Haller J. W. Beeman 《Journal of Infrared, Millimeter and Terahertz Waves》1996,17(4):669-692
We describe the design and construction of bolometric detectors for SCUBA - the Submillimetre Common-User Bolometer Array for the James Clerk Maxwell Telescope in Hawaii. The instrument contains 131 individual detectors, in two arrays, optimized for the submillimetre atmospheric transmission windows. The detectors are cooled by dilution refrigeration to a temperature of 100 mK, so that the receiver performance will be limited by photon noise from the sky and telescope background in all wavebands. A future paper will describe the performance of the detectors with reference to typical data obtained during the laboratory commissioning period. 相似文献
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In light of the pivotal role that PPARgamma2 plays in the expression of fat specific genes (e.g., A-FABP), we have examined the hypothesis that a rise in PPARgamma2 protein is required for the expression of A-FABP, and that the acceleration of fat cell differentiation by the thiazolidinedione agent, pioglitazone (PIOG), reflects an increase in the abundance of PPARgamma2 mRNA and protein. Western analyses surprisingly revealed that undifferentiated 3T3-L1 fibroblasts contained significant levels of PPARgamma2 protein; that the amount of total cellular PPARgamma2 only increased 2-fold during differentiation; and that the levels of PPARgamma2 protein and mRNA were not increased by PIOG even though fat cell differentiation was accelerated by PIOG as revealed by a 20-fold increase in A-FABP expression. Cell fractionation studies revealed that PPARgamma2 was evenly distributed between the cytosolic and nuclear compartments in both undifferentiated and differentiating 3T3-L1 cells. Immunocytochemical studies with a PPARgamma2-specific antibody indicated that PPARgamma2 was diffusely distributed throughout the cytosol of undifferentiated 3T3-L1 cells, but as the differentiation progressed, the PPARgamma2 became focused around the developing lipid droplets. In contrast to PPARgamma2, undifferentiated 3T3-L1 cells contained no measurable quantities of RXRalpha, but once fat cell differentiation was initiated by treatment with IBMX and dexamethasone, the cellular content of RXRalpha increased several fold. The rise in RXRalpha content paralleled the induction of A-FABP, but the expression of RXRalpha was not enhanced by PIOG. Although the amount of PPARgamma2 and RXRalpha was unaffected by PIOG, gel shift assays revealed that PIOG stimulated PPARgamma2/RXRalpha binding to the adipose response element of A-FABP by 5-fold in less than 12 h. Apparently, RXRalpha rather than PPARgamma2 is the pivotal trans-factor essential for the initiation of terminal fat cell differentiation. However, the high cytsolic content of PPARgamma2 and its association with the lipid droplet of differentiating 3T3-L1 cells suggests PPARgamma2 may possess a cytosolic function in the developing fat cell. 相似文献
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Tests have been made with over 300 dyed or pigmented materials exposed to mercury-tungsten or mercury lamps. The colorations were of a wide range of hue and light-fastness properties (1 to 8 and above) and in several depths on different substrates. The mercury-tungsten fluorescent lamp (500 W) gave results identical with those obtained with daylight or xenon arclight for 75% of the very varied selection of 174 patterns examined, and 25 % were within one-half of a grade, except for five which differed by one grade. When the blue standards are faded in this lamp (at 45% r.h.), they have an average interval factor of about 2.1. The required times of exposure are similar to those for the xenon arclight. The equipment required is extremely simple, and its initial and operating costs are considerably lower than those of methods hitherto used for testing in artificial light. The equipment can readily be used on the laboratory bench and is suitable for routine testing of the light fastness of any coloured material. In addition to the control of humidity, temperature control is possible, though this is not usually necessary. The mercury-vapour lamp (400 W) has also been similarly examined, using 138 patterns. It is not recommended for general use but is valuable for routine sorting tests of materials of very high fastness (BS grading above 7). The blue standard patterns fade, under exposure to these lamps, in the same sequence and with similar interval spacings, as in daylight or xenon light. 相似文献
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Lynne Baillie Lee Morton David C. Moffat Stephen Uzor 《Personal and Ubiquitous Computing》2011,15(1):13-24
Location-based games offer opportunities for us to learn more about people’s interactions and feelings towards the environment
they are in as well as to understand more about the mental models and locations associated with known environments, e.g. a
university campus with its associations of learning. In our study, we wanted to manipulate the activities in a game to take
advantage of certain locations in the hope of producing certain emotional reactions. However, it is not enough to simply produce
these reactions; one must also have a way of capturing any emotions produced whether these are the ones expected or not. The
objective of this paper, therefore, was to trial a new methodology for location-based games that aims at capturing the players’
emotional reactions to the activities in a game whilst in certain locations. In order to test the methodology, we designed
a location-based game that can be played on any Bluetooth-enabled mobile phone that has an accelerometer. The game has been
designed to interweave with a persons’ normal activity. As a result, there is little distinction between gaming time and non-gaming
time. 相似文献
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Despite recent advances in the application of data-dependent liquid chromatography/tandem mass spectrometry (LC/MS/MS) to the identification of drug metabolites in complex biological matrixes, a prior knowledge of the likely routes of biotransformation of the therapeutic agent of interest greatly facilitates the detection and structural characterization of its metabolites. Thus, prediction of the [M + H]+ m/z values of expected metabolites allows for the construction of user-defined MS(n) protocols that frequently reveal the presence of minor drug metabolites, even in the presence of a vast excess of coeluting endogenous constituents. However, this approach suffers from inherent user bias, as a result of which additional "survey scans" (e.g., precursor ion and constant neutral loss scans) are required to ensure detection of as many drug-related components in the sample as possible. In the present study, a novel approach to this problem has been evaluated, in which knowledge-based predictions of metabolic pathways are first derived from a commercial database, the output from which is used to formulate a list-dependent LC/MS(n) data acquisition protocol. Using indinavir as a model drug, a substructure similarity search on the MDL metabolism database with a similarity index of 60% yielded 188 "hits", pointing to the possible operation of two hydrolytic, two N-dealkylation, three N-glucuronidation, one N-methylation, and several aromatic and aliphatic oxidation pathways. Integration of this information with data-dependent LC/MS(n) analysis using an ion trap mass spectrometer led to the identification of 18 metabolites of indinavir following incubation of the drug with human hepatic postmitochondrial preparations. This result was accomplished with only a single LC/MS(n) run, representing significant savings in instrument use and operator time, and afforded an accurate view of the complex in vitro metabolic profile of this drug. 相似文献
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In this study, treatment efficacies of a nonionic surfactant vesicle formulation of sodium stibogluconate (SSG-NIV) and of several formulations of amphotericin B were compared in a murine model of visceral leishmaniasis. Treatment with multiple doses of AmBisome, Abelcet, and Amphocil (total dose, 12.5 mg of amphotericin B/kg of body weight) resulted in a significant suppression of parasite burdens in liver (P < 0.0005) and spleen (P < 0.0005) compared with those of controls, with Abelcet having the lowest activity. Only AmBisome and Amphocil gave significant suppression of parasites in bone marrow (compared to control values, P < 0.005). In the acute-infection model, single-dose treatments of SSG-NIV (296 mg of SbV/kg), SSG solution (296 mg of SbV/kg), or AmBisome (8 mg of amphotericin B/kg) were equally effective against liver parasites (compared to control values, P < 0.0005). SSG-NIV and AmBisome treatment also significantly suppressed parasites in bone marrow and spleen (P < 0.005), with SSG-NIV treatment being more suppressive (>98% suppression in all three sites). Free-SSG treatment failed to suppress spleen or bone marrow parasites. Infection status influenced treatment outcome. In the chronic-infection model, the AmBisome single-dose treatment was less effective in all three infection sites and the SSG-NIV single-dose treatment was less effective in the spleen. The results of this study suggest that the antileishmanial efficacy of SSG-NIV compares favorably with those of the novel amphotericin B formulations. 相似文献