Temperature dependence of the axial magnetic effect in two-color quenched QCD

The axial magnetic effect is the generation of an equilibrium dissipationless energy flow of chiral fermions in the direction of the axial (chiral) magnetic field. At finite temperature the dissipationless energy transfer may be realized in the absence of any chemical potentials. We numerically study the temperature behavior of the axial magnetic effect in quenched SUd2_ lattice gauge theory. We show that in the confinement (hadron) phase the effect is absent. In the deconfinement transition region the conductivity quickly increases, reaching the asymptotic T2 behavior in a deep deconfinement (plasma) phase. Apart from an overall proportionality factor, our results qualitatively agree with theoretical predictions for the behavior of the energy flow as a function of temperature and strength of the axial magnetic field

Axial magnetic effect in two-color quenched lattice QCD

The Axial Magnetic Effect manifests itself as an equilibrium energy flow of massless fermions induced by the axial (chiral) magnetic field. Here we study the Axial Magnetic Effect in the quenched SU(2) lattice gauge theory with massless overlap fermions at finite temperature. We numerically observe that in the low-temperature hadron phase the effect is absent due to the quark confinement. In the high-temperature deconfinement phase the energy flow is an increasing function of the temperature which reaches the predicted asymptotic T2 behavior at high temperatures. We find, however, that energy flow is about one order of magnitude lower compared to a theoretical prediction

Temperature dependence of the axial magnetic effect in two-color quenched QCD

The Axial Magnetic Effect is the generation of an equilibrium dissipationless energy flow of chiral fermions in the direction of the axial (chiral) magnetic field. At finite temperature the dissipationless energy transfer may be realized in the absence of any chemical potentials. We numerically study the temperature behavior of the Axial Magnetic Effect in quenched SU(2) lattice gauge theory. We show that in the confinement (hadron) phase the effect is absent. In the deconfinement transition region the conductivity quickly increases, reaching the asymptotic $T^2$ behavior in a deep deconfinement (plasma) phase. Apart from an overall proportionality factor, our results qualitatively agree with theoretical predictions for the behavior of the energy flow as a function of temperature and strength of the axial magnetic field.Comment: 5 pages, 1 figur

Instrumentation for Millimeter-wave Magnetoelectrodynamic Investigations of Low-Dimensional Conductors and Superconductors

We describe instrumentation for conducting high sensitivity millimeter-wave cavity perturbation measurements over a broad frequency range (40-200 GHz) and in the presence of strong magnetic fields (up to 33 tesla). A Millimeter-wave Vector Network Analyzer (MVNA) acts as a continuously tunable microwave source and phase sensitive detector (8-350 GHz), enabling simultaneous measurements of the complex cavity parameters (resonance frequency and Q-value) at a rapid repetition rate (approx. 10 kHz). We discuss the principal of operation of the MVNA and the construction of a probe for coupling the MVNA to various cylindrical resonator configurations which can easily be inserted into a high field magnet cryostat. We also present several experimental results which demonstrate the potential of the instrument for studies of low-dimensional conducting systems.Comment: 20 pages including fig

Development of a real-time PCR for the specific detection of Waddlia chondrophila in clinical samples

Waddlia chondrophila is considered as an emerging human pathogen likely involved in miscarriage and lower respiratory tract infections. Given the low sensitivity of cell culture to recover such an obligate intracellular bacteria, molecular-based diagnostic approaches are warranted. We thus developed a real-time PCR that amplifies Waddlia chondrophila DNA. Specific primers and probe were selected to target the 16S rRNA gene. The PCR specifically amplified W. chondrophila but did not amplify other related-bacteria such as Parachlamydia acanthamoebae, Simkania negevensis and Chlamydia pneumoniae. The PCR exhibited a good intra-run and inter-run reproducibility and a sensitivity of less than ten copies of the positive control. This real-time PCR was then applied to 32 nasopharyngeal aspirates taken from children with bronchiolitis not due to respiratory syncytial virus (RSV). Three samples revealed to be Waddlia positive, suggesting a possible role of this Chlamydia-related bacteria in this settin

Gene transfer of cytoprotective and immunomodulatory molecules for prevention of cardiac allograft rejection

Current treatments of heart transplantation are limited by incomplete effectiveness, significant toxicity, and failure to prevent chronic rejection. Genetic manipulation of the donor heart at the time of removal offers the unique opportunity to produce a therapeutic molecule within the graft itself, while minimizing systemic effects. Cytoprotective approaches including gene transfer of heme oxygenase (HO)-1, endothelial nitric oxide synthase, and antisense oligodeoxynucleotides specific for nuclear factor (NF)-κB or intercellular adhesion molecule (ICAM)-1 reduced ischaemia-reperfusion injury and delayed cardiac allograft rejection in small animals. Exogenous overexpression of immunomodulatory cytokines such as interleukin (IL)-4, IL-10 and transforming growth factor-β, as well as gene transfer of inhibitors of pro-inflammatory cytokines also delayed graft rejection. Gene transfer-based blockade of T-cell costimulatory activation with CTLA4-Ig or CD40-Ig resulted in long-lasting graft survival and donor-specific unresponsiveness, as manifested by acceptance of a second graft from the original donor strain but rejection of third-party grafts. Similar results were obtained with donor major histocompatibility complex class I gene transfer into bone marrow cells. Gene therapy approaches to chronic rejection included gene transfer of HO-1, soluble Fas, tissue plasminogen activator and antisense oligodeoxynucleotides specific for the anti-apoptotic mediator Bcl-x or the E2F transcription factor. Despite major experimental advances, however, gene therapy for heart transplantation has not entered the clinical arena yet. Fundamental questions regarding the most suitable vector, the best gene, and safety issues remain unanswered. Well-controlled studies that compare gene therapy with established treatments in non-human primates are needed before clinical trials can be starte

Special formulas involving polygonal numbers and Horadam numbers

Some convolution-type identities involving polygonal numbers and Horadam numbers are derived. The method of proof is to properly relate the generating functions to each other. Additionally, we prove a general non-convolutional result involving these number families and discuss some of the consequences

Cancer Tissue Engineering: A Novel 3D Polystyrene Scaffold for In Vitro Isolation and Amplification of Lymphoma Cancer Cells from Heterogeneous Cell Mixtures

Isolation and amplification of primary lymphoma cells in vitro setting is technically and biologically challenging task. To optimize culture environment and mimic in vivo conditions, lymphoma cell lines were used as a test case and were grown in 3-dimension (3D) using a novel 3D tissue culture polystyrene scaffold with neonatal stromal cells to represent a lymphoma microenvironment. In this model, the cell proliferation was enhanced more than 200-fold or 20,000% neoplastic surplus in 7 days when less than 1% lymphoma cells were cocultured with 100-fold excess of neonatal stroma cells, representing 3.2-fold higher proliferative rate than 2D coculture model. The lymphoma cells grew and aggregated to form clusters during 3D coculture and did not maintained the parental phenotype to grow in single-cell suspension. The cluster size was over 5-fold bigger in the 3D coculture by day 4 than 2D coculture system and contained less than 0.00001% of neonatal fibroblast trace. This preliminary data indicate that novel 3D scaffold geometry and coculturing environment can be customized to amplify primary cancer cells from blood or tissues related to hematological cancer and subsequently used for personalized drug screening procedures