431 research outputs found
Spin flip from dark to bright states in InP quantum dots
We report measurements of the time for spin flip from dark (non-light
emitting) exciton states in quantum dots to bright (light emitting) exciton
states in InP quantum dots. Dark excitons are created by two-photon excitation
by an ultrafast laser. The time for spin flip between dark and bright states is
found to be approximately 200 ps, independent of density and temperature below
70 K. This is much shorter than observed in other quantum dot systems. The rate
of decay of the luminescence intensity, approximately 300 ps, is not simply
equal to the radiative decay rate from the bright states, because the rate of
decay is limited by the rate of conversion from dark excitons into bright
excitons. The dependence of the luminescence decay time on the spin flip time
is a general effect that applies to many experiments.Comment: 3 figure
The Utility of Video Diaries for Organizational Research
This article assesses the utility of video diaries as a method for organization studies. While it is frequently suggested that video-based research methodologies have the capacity to capture new data about the minutiae of complex organizational affairs, as well as offering new forms of dissemination to both academic and professional audiences, little is known about the specific benefits and drawbacks of video diaries. We compare video diaries with two established and “adjacent” methods: traditional diary studies (written or audio) and other video methods. We evaluate each in relation to three key research areas: bodily expressions, identity, and practice studies. Our assessment of video diaries suggests that the approach is best used as a complement to other forms of research and is particularly suited to capturing plurivocal, asynchronous accounts of organizational phenomena. We use illustrations from an empirical research project to exemplify our claims before concluding with five points of advice for researchers wishing to employ this method
Search for Anisotropy of Ultra-High Energy Cosmic Rays with the Telescope Array Experiment
We study the anisotropy of Ultra-High Energy Cosmic Ray (UHECR) events
collected by the Telescope Array (TA) detector in the first 40 months of
operation. Following earlier studies, we examine event sets with energy
thresholds of 10 EeV, 40 EeV, and 57 EeV. We find that the distributions of the
events in right ascension and declination are compatible with an isotropic
distribution in all three sets. We then compare with previously reported
clustering of the UHECR events at small angular scales. No significant
clustering is found in the TA data. We then check the events with E>57 EeV for
correlations with nearby active galactic nuclei. No significant correlation is
found. Finally, we examine all three sets for correlations with the large-scale
structure of the Universe. We find that the two higher-energy sets are
compatible with both an isotropic distribution and the hypothesis that UHECR
sources follow the matter distribution of the Universe (the LSS hypothesis),
while the event set with E>10 EeV is compatible with isotropy and is not
compatible with the LSS hypothesis at 95% CL unless large deflection angles are
also assumed. We show that accounting for UHECR deflections in a realistic
model of the Galactic magnetic field can make this set compatible with the LSS
hypothesis.Comment: 10 pages, 9 figure
Surface Affinity of the Hydronium Ion: The Effective Fragment Potential and Umbrella Sampling
The surface affinity of the hydronium ion in water is investigated with umbrella sampling and classical molecular dynamics simulations, in which the system is described with the effective fragment potential (EFP). The solvated hydronium ion is also explored using second order perturbation theory for the hydronium ion and the empirical TIP5P potential for the waters. Umbrella sampling is used to analyze the surface affinity of the hydronium ion, varying the number of solvent water molecules from 32 to 256. Umbrella sampling with the EFP method predicts the hydronium ion to most probably lie about halfway between the center and edge of the water cluster, independent of the cluster size. Umbrella sampling using MP2 for the hydronium ion and TIP5P for the solvating waters predicts that the solvated proton most probably lies about 0.5–2.0 Å from the edge of the water cluster independent of the cluster size
1, 9-Pyrazoloanthrones Downregulate HIF-1α and Sensitize Cancer Cells to Cetuximab-Mediated Anti-EGFR Therapy
Cetuximab, a monoclonal antibody that blocks the epidermal growth factor receptor (EGFR), is currently approved for the treatment of several types of solid tumors. We previously showed that cetuximab can inhibit hypoxia-inducible factor-1 alpha (HIF-1α) protein synthesis by inhibiting the activation of EGFR downstream signaling pathways including Erk, Akt, and mTOR. 1, 9-pyrazoloanthrone (1, 9 PA) is an anthrapyrazolone compound best known as SP600125 that specifically inhibits c-jun N-terminal kinase (JNK). Here, we report 1, 9 PA can downregulate HIF-1α independently of its inhibition of JNK. This downregulatory effect was abolished when the oxygen-dependent domain (ODD) of HIF-1α (HIF-1α-ΔODD, the domain responsible for HIF-1α degradation) was experimentally deleted or when the activity of HIF-1α prolyl hydroxylase (PHD) or the 26S proteasomal complex was inhibited, indicating that the 1, 9 PA downregulates HIF-1α by promoting PHD-dependent HIF-1α degradation. We found that the combination of 1, 9 PA and cetuximab worked synergistically to induce apoptosis in cancer cells in which cetuximab or 1, 9 PA alone had no or only weak apoptotic activity. This synergistic effect was substantially decreased in cancer cells transfected with HIF-1α-ΔODD, indicating that downregulation of HIF-1α was the mechanism of this synergistic effect. More importantly, 1, 9 PA can downregulate HIF-1α in cancer cells that are insensitive to cetuximab-induced inhibition of HIF-1α expression due to overexpression of oncogenic Ras (RasG12V). Our findings suggest that 1, 9 PA is a lead compound of a novel class of drugs that may be used to enhance the response of cancer cells to cetuximab through a complementary effect on the downregulation of HIF-1α
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