968 research outputs found
Enzyme kinetics for a two-step enzymic reaction with comparable initial enzyme-substrate ratios
We extend the validity of the quasi-steady state assumption for a model double intermediate enzyme-substrate reaction to include the case where the ratio of initial enzyme to substrate concentration is not necessarily small. Simple analytical solutions are obtained when the reaction rates and the initial substrate concentration satisfy a certain condition. These analytical solutions compare favourably with numerical solutions of the full system of differential equations describing the reaction. Experimental methods are suggested which might permit the application of the quasi-steady state assumption to reactions where it may not have been obviously applicable before
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Magnetic characterization of perpendicular recording media
In this paper, we describe techniques for the magnetic characterization of perpendicular recording media. Such measurements made using traditional techniques, such as the vibrating sample magnetometry (VSM) and alternating gradient force magnetometer (AGFM), have to be corrected for the sample shape demagnetizing factor, which is often found not to be equal to -4p. For measurements other than the simple hysteresis loop, such as remanence curves, this correction must be carried out in real time and we describe the method by which this can be achieved and the process for achieving the correct demagnetization of perpendicular films prior to measurements of the isothermal remanent magnetization curve. A further complication is that real perpendicular media have a soft underlayer beneath the recording layer, which swamps and confuses signals from instruments such as VSM or AGFM. Hence, we describe the construction and use of a magnetooptical Kerr effect magnetometer, which does not penetrate significantly into the soft layer and enables the perpendicular layer to be measured independently. We describe the properties of a traditional alloy perpendicular medium and a Co-Pd multilayer system, which in the latter case exhibits multiple switching behavior. We also address the issue of the effect of the soft underlayer on the coupling in similar longitudinal films and find that the presence of the underlayer induces significant additional coupling effects that may well give rise to an increase in noise in recorded signal
Blocking Epidermal Growth Factor Receptor Signaling in HTR-8/SVneo First Trimester Trophoblast Cells Results in Dephosphorylation of PKBα/AKT and Induces Apoptosis
We identified a major peptide signaling target of EGF/EGFR pathway and explored the consequences of blocking or activating this pathway in the first trimester extravillous trophoblast cells, HTR-8/SVneo. A global analysis of protein phosphorylation was undertaken using novel technology (Kinexus Kinetworks) that utilizes SDS-polyacrylamide minigel electrophoresis and multi-lane immunoblotting to permit specific and semiquantitative detection of multiple phosphoproteins. Forty-seven protein phosphorylation sites were queried, and the results reported based on relative phosphorylation at each site. EGF- and Iressa-(gefitinib, ZD1839, an inhibitor of EGFR) treated HTR-8/SVneo cells were subjected to immunoblotting and flow cytometry to confirm the phosphoprotein screen and to assess the effects of EGF versus Iressa on cell cycle and apoptosis. EGFR mediates the phosphorylation of important signaling proteins, including PKBα/AKT. This pathway is likely to be central to EGFR-mediated trophoblast survival. Furthermore, EGF treatment induces proliferation and inhibits apoptosis, while Iressa induces apoptosis
Molecular formations in ultracold mixtures of interacting and noninteracting atomic gases
Atom-molecule equilibrium for molecular formation processes is discussed for
boson-fermion, fermion-fermion, and boson-boson mixtures of ultracold atomic
gases in the framework of quasichemical equilibrium theory. After presentation
of the general formulation, zero-temperature phase diagrams of the
atom-molecule equilibrium states are calculated analytically; molecular, mixed,
and dissociated phases are shown to appear for the change of the binding energy
of the molecules. The temperature dependences of the atom or molecule densities
are calculated numerically, and finite-temperature phase structures are
obtained of the atom-molecule equilibrium in the mixtures. The transition
temperatures of the atom or molecule Bose-Einstein condensations are also
evaluated from these results. Quantum-statistical deviations of the law of mass
action in atom-molecule equilibrium, which should be satisfied in mixtures of
classical Maxwell-Boltzmann gases, are calculated, and the difference in the
different types of quantum-statistical effects is clarified. Mean-field
calculations with interparticle interactions (atom-atom, atom-molecule, and
molecule-molecule) are formulated, where interaction effects are found to give
the linear density-dependent term in the effective molecular binding energies.
This method is applied to calculations of zero-temperature phase diagrams,
where new phases with coexisting local-equilibrium states are shown to appear
in the case of strongly repulsive interactions.Comment: 35 pages, 14 figure
First-principles kinetic Monte Carlo simulations for heterogeneous catalysis, applied to the CO oxidation at RuO2(110)
We describe a first-principles statistical mechanics approach enabling us to
simulate the steady-state situation of heterogeneous catalysis. In a first step
density-functional theory together with transition-state theory is employed to
obtain the energetics of all relevant elementary processes. Subsequently the
statistical mechanics problem is solved by the kinetic Monte Carlo method,
which fully accounts for the correlations, fluctuations, and spatial
distributions of the chemicals at the surface of the catalyst under
steady-state conditions. Applying this approach to the catalytic oxidation of
CO at RuO2(110), we determine the surface atomic structure and composition in
reactive environments ranging from ultra-high vacuum (UHV) to technologically
relevant conditions, i.e. up to pressures of several atmospheres and elevated
temperatures. We also compute the CO2 formation rates (turnover frequencies).
The results are in quantitative agreement with all existing experimental data.
We find that the high catalytic activity of this system is intimately connected
with a disordered, dynamic surface ``phase'' with significant compositional
fluctuations. In this active state the catalytic function results from a
self-regulating interplay of several elementary processes.Comment: 18 pages including 9 figures; related publications can be found at
http://www.fhi-berlin.mpg.de/th/th.htm
Nonequilibrium orientational patterns in two-component Langmuir monolayers
A model of a phase-separating two-component Langmuir monolayer in the
presence of a photo-induced reaction interconvering two components is
formulated. An interplay between phase separation, orientational ordering and
treaction is found to lead to a variety of nonequilibrium self-organized
patterns, both stationary and traveling. Examples of the patterns, observed in
numerical simulations, include flowing droplets, traveling stripes, wave
sources and vortex defects.Comment: Submitted to the Physical Review
Hawtreyan 'credit deadlock' or Keynesian 'liquidity trap'? Lessons for Japan from the great depression
This paper outlines the ideas of Ralph Hawtrey and Lauchlin Currie on the need for monetised fiscal deficit spending in 1930s USA to combat the deep depression into which the economy had been allowed to sink. In such exceptional circumstances of 'credit deadlock' in which banks were afraid to lend and households and business afraid to borrow, the deadlock could best be broken through the spending of new money into circulation via large fiscal deficits. This complementarity of fiscal and monetary policy was shown to be essential, and as such indicates the potential power of monetary policy - in contrast to the Keynesian "liquidity trap" view that it is powerless This lesson was not learned by the Japanese authorities in their response to the asset price collapse of 1991-92, resulting in a lost decade as ballooning fiscal deficits were neutralised throughout the 1990s by unhelpfully tight monetary policy with the Bank of Japan refusing to monetise the deficits
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Chemical Technology Division. Annual technical report, 1995
Highlights of the Chemical Technology (CMT) Division`s activities during 1995 are presented. In this period, CMT conducted research and development in the following areas: (1) electrochemical technology, including advanced batteries and fuel cells; (2) methods for treatment of hazardous waste and mixed hazardous/radioactive waste; (3) the reaction of nuclear waste glass and spent fuel under conditions expected for an unsaturated repository; (4) processes for separating and recovering selected elements from waste streams, concentrating low-level radioactive waste streams with advanced evaporator technology, and producing {sup 99}Mo from low-enriched uranium; (5) electrometallurgical treatment of different types of spent nuclear fuel in storage at Department of Energy sites; and (6) physical chemistry of selected materials in environments simulating those of fission and fusion energy systems
Two-Species Annihilation with Drift: A Model with Continuous Concentration-Decay Exponents
We propose a model for diffusion-limited annihilation of two species, or , where the motion of the particles is subject to a drift. For equal
initial concentrations of the two species, the density follows a power-law
decay for large times. However, the decay exponent varies continuously as a
function of the probability of which particle, the hopping one or the target,
survives in the reaction. These results suggest that diffusion-limited
reactions subject to drift do not fall into a limited number of universality
classes.Comment: 10 pages, tex, 3 figures, also available upon reques
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