Finishing the euchromatic sequence of the human genome

The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead

A Comparison Between FAST and SPS Apparatuses Based on the Sintering of Oxide Ceramics

Field-assisted sintering technique (FAST) and spark plasma sintering (SPS) apparatuses are based on the same technical principles, but differ in design. A current flows directly through the graphite pressing tool, which acts as heating element in both machines. The main differences are the pressing tool geometry and material, current pulsing and the position of the temperature measurements. Tests under identical conditions (same heating schedule, applied load, and pressing tool, as well as similar pulse patterns) were conducted on both types of set-ups. Three different oxide materials were tested: alumina, 8 mol% yttria-stabilized zirconia (8YSZ) and zinc oxide

Multimodal grain size distribution and high hardness in fine grained tungsten fabricated by spark plasma sintering

Preparation of fine grained, hard and ductile pure tungsten for future fusion reactor applications was tested using the bottom-up approach via powder consolidation by spark plasma sintering (SPS) at different temperature (1300-1800 degrees C) and pressure (90-266 MPa) conditions. Pure tungsten powders with an average particle size of about 1 mu m were sintered to high density (about 94%) with almost no grain growth at a temperature below 1400 degrees C and an applied pressure up to 266 MPa. These samples had a multi-modal grain size distribution (resembling the size distribution of the initial powder) and a very high Vickers hardness (up to 530 kg/mm(2)). Above 1500 degrees C fast grain growth occurred and resulted in a drop in hardness. XRD on the surface of bulk samples showed a small amount of tungsten oxides; however, XPS and EDS indicated that these oxides were only surface contaminants and suggested a high purity for the bulk samples. The results demonstrate that SPS can lead to ultrafine and nanocrystalline tungsten if used to consolidate pure nano tungsten powders. (C) 2011 Elsevier B.V. All rights reserved

Integration of a (6)LilnSe(2) thermal neutron detector into a CubeSat instrument

We present a preliminary design for a neutron detection system that is compact, lightweight, and low power consuming, utilizing the CubeSat platform making it suitable for space-based applications. This is made possible using the scintillating crystal lithium indium diselenide ((LiInSe2)-Li-6), the first crystal to include Li-6 in the crystalline structure, and a silicon avalanche photodiode. The schematics of this instrument are presented as well as the response of the instrument to initial testing under alpha radiation. A principal aim of this work is to demonstrate the feasibility of such a neutron detection system within a CubeSat platform. The entire end-to-end system presented here is 10 x 10 x 15 cm(3), weighs 670 g, and requires 5 V direct current at 3 W. (C) 2016 Society of Photo-Optical Instrumentation Engineers (SPIE)National Science Foundation [AST-0849736]This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at [email protected]

Neutron detector development for microsatellites

We present a preliminary design for a novel neutron detection system that is compact, lightweight, and low power consuming, utilizing the CubeSat platform making it suitable for space-based applications. This is made possible using the scintillating crystal lithium indium diselenide ((LiInSe2)-Li-6), the first crystal to include Li-6 in the crystalline structure, and a silicon avalanche photodiode (Si-APD). The schematics of this instrument are presented as well as the response of the instrument to initial testing under alpha, gamma and neutron radiation. A principal aim of this work is to demonstrate the feasibility of such a neutron detection system within a CubeSat platform. The entire end-to-end system presented here is 10 cm x 10 cm x 15 cm, weighs 670 grams and requires 5 V direct current at 3 Watts.This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at [email protected]

Sigma-2 receptor and progesterone receptor membrane component 1 (PGRMC1) are two different proteins: Proofs by fluorescent labeling and binding of sigma-2 receptor ligands to PGRMC1

A controversial relationship between sigma-2 and progesterone receptor membrane component 1 (PGRMC1) proteins, both representing promising targets for the therapy and diagnosis of tumors, exists since 2011, when the sigma-2 receptor was reported to be identical to PGRMC1. Because a misidentification of these proteins will lead to biased future research hampering the possible diagnostic and therapeutic exploitation of the two targets, there is the need to solve the debate on their identity. With this aim, we have herein investigated uptake and distribution of structurally different fluorescent sigma-2 receptor ligands by flow cytometry and confocal microscopy in MCF7 cells, where together with intrinsic sigma-2 receptors, PGRMC1 was constitutively present or alternatively silenced or overexpressed. HCT116 cells, with constitutive or silenced PGRMC1, were also studied. These experiments showed that the fluorescent sigma-2 ligands bind to their receptor irrespective of PGRMC1 expression. Furthermore, isothermal titration calorimetry was conducted to examine if DTG and PB28, two structurally distinct nanomolar affinity sigma-2 ligands, bind to purified PGRMC1 proteins that have recently been revealed to form both apo-monomeric and heme-mediated dimeric forms. While no binding to apo-PGRMC1 monomer was detected, a micromolar affinity to heme-mediated dimerized PGRMC1 was demonstrated in DTG but not in PB28. The current data provide evidence that sigma-2 receptor and PGRMC1 are not identical, paving the pathway for future unbiased research in which these two attractive targets are treated as different proteins while the identification of the true sigma-2 protein further needs to be pursued