On the longitudinal structure function in the dipole model

We compare new HERA data for the longitudinal structure function $F_{\rm L}$ with the predictions of different variants of the dipole model. In particular we show that the ratio $F_{\rm L}/F_2$ is well described by the dipole models and is rather insensitive to the details of the fit. Fits to $F_2$ are performed with the help of geometrical scaling (GS). Using the property of GS we derive the bounds for $F_{\rm L}/F_2$ both for the different versions of the dipole model and in the general case. Finally we briefly discuss how the higher Fock components of the photon wave function may affect these bounds.Comment: 19 pages, 11 figures, v3 to be published in Acta Physica Polonica

Structure and Dynamics of High Temperature Superconductors

High temperature superconductivity in iron based compounds has presented a series of complex problems to condensed matter physics since being discovered in 2008. The stalwart basis of condensed matter physics is the “strength in numbers aspect of crystalline periodicity. Perfect crystalline periodicity has made possible the reduction of the questions of structural and electronic properties to single dimensions, increasing the tractability of these problems. Nevertheless, modern complex materials stretch these assumptions to their limits, and it is at this point where our work starts. Using neutron and x-ray scattering, we have conducted a series of studies on the structural disorder of iron based superconductors and found it to be ubiquitous. Further, we have investigated the lattice dynamics of the iron-based superconducting systems, and found anomalous phonon behavior, with coupling between the spin and lattice degrees of freedom. These findings together raise questions on the role of structural disorder in complex materials, high temperature superconductivity specifically

Perfomance analysis of libraries for testing web applications on the ASP.NET Core platform

This paper conducts a performance analysis of three libraries: XUnit, NUnit, MSTest, aiming to compare the time performance. The performance was checked using load test, synchronous and asynchronous tests. The synchronous and asynchronous tests were divided into groups of 10, 25, 50 and 100 test cases. The tests were carried out using an inhouse project written on the ASP.NET Core platform

Primary results of 2-dimensional electrophoresis for protein studies of Gentiana kurroo Royle somatic embryos derived from long-term embryogenic cell suspensions

Two-dimensional gel electrophoresis was used to compare protein expression profiles between various stages of Gentiana kurroo Royle somatic embryos. Seven distinct stages (I–VII) were pointed out and measured from long-term embryogenic cell suspension. Isoelectric focusing was done in the pH intervals 3–10, and the second dimension was carried out with 13% SDS-polyacrylamide gel electrophoresis. Dependent on the stage from about 400 (stage IV) to more than 700 (stage II) protein spots were totally detected. The molecular weight of abundant proteins range from 12 to 70 kDa, however, majority of proteins were located between 20–49 kDa spots on the gels. The highest difference in the number of spots appeared in the case of globular embryo (stage I) and elongated cotyledonary stage (stage VII) with differences being about 130 spots. The relevance of embryogenic cell suspension choice for proteomic analysis as well as expediency of the increasing number of particular embryo stages is discussed

Primary results of 2-dimensional electrophoresis for protein studies of Gentiana kurroo Royle somatic embryos derived from long-term embryogenic cell suspensions

Two-dimensional gel electrophoresis was used to compare protein expression profiles between various stages of Gentiana kurroo Royle somatic embryos. Seven distinct stages (I–VII) were pointed out and measured from long-term embryogenic cell suspension. Isoelectric focusing was done in the pH intervals 3–10, and the second dimension was carried out with 13% SDS-polyacrylamide gel electrophoresis. Dependent on the stage from about 400 (stage IV) to more than 700 (stage II) protein spots were totally detected. The molecular weight of abundant proteins range from 12 to 70 kDa, however, majority of proteins were located between 20–49 kDa spots on the gels. The highest difference in the number of spots appeared in the case of globular embryo (stage I) and elongated cotyledonary stage (stage VII) with differences being about 130 spots. The relevance of embryogenic cell suspension choice for proteomic analysis as well as expediency of the increasing number of particular embryo stages is discussed