169 research outputs found

    Automated quantitative analysis of single and double label autoradiographs

    Get PDF
    A method for the analysis of silver grain content in both single and double label autoradiographs is presented. The total grain area is calculated by counting the number of pixels at which the recorded light intensity in transmission dark field illumination exceeds a selected threshold. The calibration tests included autoradiographs with low (3H- thymidin) and high (3H-desoxyuridin) silver grain density. The results are proportional to the customary visual grain count. For the range of visibly countable grain densities in single labeled specimens, the correlation coefficient between the computed values and the visual grain counts is better than 0.96. In the first emulsion of the two emulsion layer autoradiographs of double labeled specimens (3H-14C- thymidin) the correlation coefficient is 0.919 and 0.906. The method provides a statistical correction for the background grains not due to the isotope. The possibility to record 14C tracks by shifting the focus through the second emulsion of the double labeled specimens is also demonstrated. The reported technique is essentially independent of size, shape and density of the grains

    The Seed of Principate: Annona and Imperial Politics

    Get PDF
    From my study of the annona, I propose a new perspective on the transition between the Republic and the Principate. Each of the big three imperial historians account for the Principate in terms of personal politics and preferences of the “great man” Augustus (Div. Aug. 28; Rom. His. 52.1; Ann. 1.2). By contrast, I argue that the Principate represents the long-term political result of growing social inequality in Rome. From an equalitarian society of yodel-men farmers and shepherds in the 2nd BCE, Rome had evolved into an unequal society by the 2nd CE, where the top 11.15% controlled an estimated 40% of the national income.[1] As income inequality arose, the competition between rich and poor, the optimates and populares, over the bounty of the Empire paralyzed the politics of the Roman Republic. In the deadlock of the late Republic, the Senate proved unwilling or unable to respond to the new needs of Rome and its extensive empire. Deadlock devolved into deadly civil war. To rebuild the Roman state from its ruin, Augustus and his successors created the Principate and its governance institutions on the basis of “Republican” precedent. Since Augustus could not equalize the distribution of wealth and power between the Emperor and his Senators, the Principate proved provisional. [1]Scheidel and Friesen 2009: 62

    A Tribute to Reality?

    Get PDF

    Energy Flow in the Hadronic Final State of Diffractive and Non-Diffractive Deep-Inelastic Scattering at HERA

    Get PDF
    An investigation of the hadronic final state in diffractive and non--diffractive deep--inelastic electron--proton scattering at HERA is presented, where diffractive data are selected experimentally by demanding a large gap in pseudo --rapidity around the proton remnant direction. The transverse energy flow in the hadronic final state is evaluated using a set of estimators which quantify topological properties. Using available Monte Carlo QCD calculations, it is demonstrated that the final state in diffractive DIS exhibits the features expected if the interaction is interpreted as the scattering of an electron off a current quark with associated effects of perturbative QCD. A model in which deep--inelastic diffraction is taken to be the exchange of a pomeron with partonic structure is found to reproduce the measurements well. Models for deep--inelastic epep scattering, in which a sizeable diffractive contribution is present because of non--perturbative effects in the production of the hadronic final state, reproduce the general tendencies of the data but in all give a worse description.Comment: 22 pages, latex, 6 Figures appended as uuencoded fil

    Jets and energy flow in photon-proton collisions at HERA

    Get PDF
    Properties of the hadronic final state in photoproduction events with large transverse energy are studied at the electron-proton collider HERA. Distributions of the transverse energy, jets and underlying event energy are compared to \overline{p}p data and QCD calculations. The comparisons show that the \gamma p events can be consistently described by QCD models including -- in addition to the primary hard scattering process -- interactions between the two beam remnants. The differential jet cross sections d\sigma/dE_T^{jet} and d\sigma/d\eta^{jet} are measured

    Разработка интерактивной моделирующей системы технологии низкотемпературной сепарации газа

    Get PDF
    We present a study of J ψ meson production in collisions of 26.7 GeV electrons with 820 GeV protons, performed with the H1-detector at the HERA collider at DESY. The J ψ mesons are detected via their leptonic decays both to electrons and muons. Requiring exactly two particles in the detector, a cross section of σ(ep → J ψ X) = (8.8±2.0±2.2) nb is determined for 30 GeV ≤ W γp ≤ 180 GeV and Q 2 ≲ 4 GeV 2 . Using the flux of quasi-real photons with Q 2 ≲ 4 GeV 2 , a total production cross section of σ ( γp → J / ψX ) = (56±13±14) nb is derived at an average W γp =90 GeV. The distribution of the squared momentum transfer t from the proton to the J ψ can be fitted using an exponential exp(− b ∥ t ∥) below a ∥ t ∥ of 0.75 GeV 2 yielding a slope parameter of b = (4.7±1.9) GeV −2

    Nonlinear Beam Propagation in a Class of Complex Non-PT -Symmetric Potentials

    Get PDF
    The subject of PT-symmetry and its areas of application have been blossoming over the past decade. Here, we consider a nonlinear Schr\"odinger model with a complex potential that can be tuned controllably away from being PT-symmetric, as it might be the case in realistic applications. We utilize two parameters: the first one breaks PT-symmetry but retains a proportionality between the imaginary and the derivative of the real part of the potential; the second one, detunes from this latter proportionality. It is shown that the departure of the potential from the PT -symmetric form does not allow for the numerical identification of exact stationary solutions. Nevertheless, it is of crucial importance to consider the dynamical evolution of initial beam profiles. In that light, we define a suitable notion of optimization and find that even for non PT-symmetric cases, the beam dynamics, both in 1D and 2D -although prone to weak growth or decay- suggests that the optimized profiles do not change significantly under propagation for specific parameter regimes

    A series of Fas receptor agonist antibodies that demonstrate an inverse correlation between affinity and potency

    Get PDF
    Receptor agonism remains poorly understood at the molecular and mechanistic level. In this study, we identified a fully human anti-Fas antibody that could efficiently trigger apoptosis and therefore function as a potent agonist. Protein engineering and crystallography were used to mechanistically understand the agonistic activity of the antibody. The crystal structure of the complex was determined at 1.9 Å resolution and provided insights into epitope recognition and comparisons with the natural ligand FasL (Fas ligand). When we affinity-matured the agonist antibody, we observed that, surprisingly, the higher-affinity antibodies demonstrated a significant reduction, rather than an increase, in agonist activity at the Fas receptor. We propose and experimentally demonstrate a model to explain this non-intuitive impact of affinity on agonist antibody signalling and explore the implications for the discovery of therapeutic agonists in general

    Importance of dose-schedule of 5-aza-2'-deoxycytidine for epigenetic therapy of cancer

    Get PDF
    <p>Abstract</p> <p>Background</p> <p>The inactivation of tumor suppressor genes (TSGs) by aberrant DNA methylation plays an important role in the development of malignancy. Since this epigenetic change is reversible, it is a potential target for chemotherapeutic intervention using an inhibitor of DNA methylation, such as 5-aza-2'-deoxycytidine (DAC). Although clinical studies show that DAC has activity against hematological malignancies, the optimal dose-schedule of this epigenetic agent still needs to be established.</p> <p>Methods</p> <p>Clonogenic assays were performed on leukemic and tumor cell lines to evaluate the <it>in vitro </it>antineoplastic activity of DAC. The reactivation of TSGs and inhibition of DNA methylation by DAC were investigated by reverse transcriptase-PCR and Line-1 assays. The <it>in vivo </it>antineoplastic activity of DAC administered as an i.v. infusion was evaluated in mice with murine L1210 leukemia by measurement of survival time, and in mice bearing murine EMT6 mammary tumor by excision of tumor after chemotherapy for an <it>in vitro </it>clonogenic assay.</p> <p>Results</p> <p>Increasing the DAC concentration and duration of exposure produced a greater loss of clonogenicity for both human leukemic and tumor cell lines. The reactivation of the TSGs (<it>p57KIP2 </it>in HL-60 leukemic cells and <it>p16CDKN2A </it>in Calu-6 lung carcinoma cells) and the inhibition of global DNA methylation in HL-60 leukemic cells increased with DAC concentration. In mice with L1210 leukemia and in mice bearing EMT6 tumors, the antineoplastic action of DAC also increased with the dose. The plasma level of DAC that produced a very potent antineoplastic effect in mice with leukemia or solid tumors was > 200 ng/ml (> 1 μM).</p> <p>Conclusion</p> <p>We have shown that intensification of the DAC dose markedly increased its antineoplastic activity in mouse models of cancer. Our data also show that there is a good correlation between the concentrations of DAC that reduce <it>in vitro </it>clonogenicity, reactivate TSGs and inhibit DNA methylation. These results suggest that the antineoplastic action of DAC is related to its epigenetic action. Our observations provide a strong rationale to perform clinical trials using dose intensification of DAC to maximize the chemotherapeutic potential of this epigenetic agent in patients with cancer.</p
    corecore