436 research outputs found

    イ ノ キモゾウ ニツイテ ホイ

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    Continuum-discretized coupled-channels method for four-body nuclear breakup in 6^6He+12^{12}C scattering

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    We propose a fully quantum-mechanical method of treating four-body nuclear breakup processes in scattering of a projectile consisting of three constituents, by extending the continuum-discretized coupled-channels method. The three-body continuum states of the projectile are discretized by diagonalizing the internal Hamiltonian of the projectile with the Gaussian basis functions. For 6^6He+12^{12}C scattering at 18 and 229.8 MeV, the validity of the method is tested by convergence of the elastic and breakup cross sections with respect to increasing the number of the basis functions. Effects of the four-body breakup and the Borromean structure of 6^6He on the elastic and total reaction cross sections are discussed.Comment: 5 pages, 6 figures, uses REVTeX 4, submitted to Phys. Rev.

    Are spectroscopic factors from transfer reactions consistent with asymptotic normalisation coefficients?

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    It is extremely important to devise a reliable method to extract spectroscopic factors from transfer cross sections. We analyse the standard DWBA procedure and combine it with the asymptotic normalisation coefficient, extracted from an independent data set. We find that the single particle parameters used in the past generate inconsistent asymptotic normalization coefficients. In order to obtain a consistent spectroscopic factor, non-standard parameters for the single particle overlap functions can be used but, as a consequence, often reduced spectroscopic strengths emerge. Different choices of optical potentials and higher order effects in the reaction model are also studied. Our test cases consist of: 14^{14}C(d,p)15^{15}C(g.s.) at Edlab=14E_d^{lab}=14 MeV, 16^{16}O(d,p)17^{17}O(g.s.) at Edlab=15E_d^{lab}=15 MeV and 40^{40}Ca(d,p)41^{41}Ca(g.s.) at Edlab=11E_d^{lab}=11 MeV. We underline the importance of performing experiments specifically designed to extract ANCs for these systems.Comment: 15 pages, 12 figures, Phys. Rev. C (in press

    Inelastic scattering of protons from 6,8^{6,8}He and 7,11^{7,11}Li in a folding model approach

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    The proton-inelastic scattering from 6,8^{6,8}He and 7,11^{7,11}Li nuclei are studied in a folding model approach. A finite-range, momentum, density and isospin dependent nucleon-nucleon interaction (SBM) is folded with realistic density distributions of the above nuclei. The renormalization factors NR_R and NI_I on the real and volume imaginary part of the folded potentials are obtained by analyzing the respective elastic scattering data and kept unaltered for the inelastic analysis at the same energy. The form factors are generated by taking derivatives of the folded potentials and therefore required renormalizations. The β\beta values are extracted by fitting the p + 6,8^{6,8}He,7,11^{7,11}Li inelastic angular distributions. The present analysis of p + 8^8He inelastic scattering to the 3.57 MeV excited state, including unpublished forward angle data (RIKEN) confirms L = 2 transition. Similar analysis of the p + 6^6He inelastic scattering angular distribution leading to the 1.8 MeV (L = 2) excited state fails to satisfactorily reproduce the data.Comment: one LaTeX file, five PostScript figure

    A Polymerase-chain-reaction Assay for the Specific Identification of Transcripts Encoded by Individual Carcinoembryonic Antigen (CEA)-gene-family Members

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    Carcinoembryonic antigen (CEA) is a tumor marker that belongs to a family of closely related molecules with variable expression patterns. We have developed sets of oligonucleotide primers for the specific amplification of transcripts from individual CEA-family members using the reverse transcriptase/ polymerase chain reaction (RT/PCR). Specific primer sets were designed for CEA, non-specific cross-reacting antigen (NCA), biliary glycoprotein (BGP), carcinoembryonic antigen gene-family members 1, 6 and 7 (CGMI, CGM6 and CGM7), and one set for all pregnancy-specific glycoprotein (PSG) transcripts. Primers were first tested for their specificity against individual cDNA clones and product-hybridization with internal, transcript-specific oligonucleotides. Total RNA from 12 brain and 63 gynecological tumors were then tested for expression of CEA-related transcripts. None were found in tumors located in the brain, including various mesenchymal and neuro-epithelial tumors. CEA and NCA transcripts were, however, present in an adenocarcinoma located in the nasal sinuses. In ovarian mucinous adenocarcinomas, we always found co-expression of CEA and NCA transcripts, and occasionally BGP mRNA. CEA-related transcripts were also found in some serous, endometrioid and clear-cell ovarian carcinomas. CEA, NCA and BGP transcripts were present in endometrial carcinomas of the uterus and cervical carcinomas, whereas uterine leiomyomas were completely negative. No transcripts were found from CGM 1, CGM6, CGM7 or from PSG genes in any of the tumors tested. The PCR data were compared with immunohistochemical investigations of ovarian tumors at the protein level using CEA (26/3/13)-, NCA-50/90 (9A6FR) and NCA-95 (80H3)-specific monoclonal antibodies

    A facile quantitative assay for viral particle genesis reveals cooperativity in virion assembly and saturation of an antiviral protein

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    Conventional assays of viral particle assembly and release are time consuming and laborious. We have developed an enzymatic virus-like particle (VLP) genesis assay that rapid and quantitative and is also versatile and applicable to diverse viruses including HIV-1 and Ebola virus. Using this assay, which has a dynamic range of several orders of magnitude, we show that the efficiency of VLP assembly and release, i.e., the fraction of the expressed protein that is assembled into extracellular particles, is dependent on the absolute level of expression of either HIV-1 Gag or Ebola virus VP40. We also demonstrate that the activity of the antiviral factor tetherin is dependent on the level of HIV-1 Gag expression and the numbers of VLPs generated, and appears to become saturated as these parameters are increased

    Application of Absorbing Boundary Condition to Nuclear Breakup Reactions

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    Absorbing boundary condition approach to nuclear breakup reactions is investigated. A key ingredient of the method is an absorbing potential outside the physical area, which simulates the outgoing boundary condition for scattered waves. After discretizing the radial variables, the problem results in a linear algebraic equation with a sparse coefficient matrix, to which efficient iterative methods can be applicable. No virtual state such as discretized continuum channel needs to be introduced in the method. Basic aspects of the method are discussed by considering a nuclear two-body scattering problem described with an optical potential. We then apply the method to the breakup reactions of deuterons described in a three-body direct reaction model. Results employing the absorbing boundary condition are found to accurately coincide with those of the existing method which utilizes discretized continuum channels.Comment: 21 pages, 5 figures, RevTeX
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