580 research outputs found

    Parity Nonconservation in Neutron Resonances in 133Cs

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    Spatial parity nonconservation (PNC) has been studied in the compound-nuclear states of 134Cs by measuring the helicity dependence of the neutron total cross section. Transmission measurements on a thick 133Cs target were performed by the time-of-flight method at the Manuel Lujan Neutron Scattering Center with a longitudinally polarized neutron beam in the energy range from 5 to 400 eV. A total of 28 new p-wave resonances were found, their neutron widths determined, and the PNC longitudinal asymmetries of the resonance cross sections measured. The value obtained for the root-mean-square PNC element M=(0.06-0.02+0.25) meV in 133Cs is the smallest among all targets studied. This value corresponds to a weak spreading width Γw=(0.006-0.003+0.154)×10-7 eV

    Stable vortex and dipole vector solitons in a saturable nonlinear medium

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    We study both analytically and numerically the existence, uniqueness, and stability of vortex and dipole vector solitons in a saturable nonlinear medium in (2+1) dimensions. We construct perturbation series expansions for the vortex and dipole vector solitons near the bifurcation point where the vortex and dipole components are small. We show that both solutions uniquely bifurcate from the same bifurcation point. We also prove that both vortex and dipole vector solitons are linearly stable in the neighborhood of the bifurcation point. Far from the bifurcation point, the family of vortex solitons becomes linearly unstable via oscillatory instabilities, while the family of dipole solitons remains stable in the entire domain of existence. In addition, we show that an unstable vortex soliton breaks up either into a rotating dipole soliton or into two rotating fundamental solitons.Comment: To appear in Phys. Rev.

    Application of phage display to high throughput antibody generation and characterization.

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    We have created a high quality phage display library containing over 1010 human antibodies and describe its use in the generation of antibodies on an unprecedented scale. We have selected, screened and sequenced over 38,000 recombinant antibodies to 292 antigens, yielding over 7,200 unique clones. 4,400 antibodies were characterized by specificity testing and detailed sequence analysis and the data/clones are available online. Sensitive detection was demonstrated in a bead based flow cytometry assay. Furthermore, positive staining by immunohistochemistry on tissue microarrays was found for 37% (143/381) of antibodies. Thus, we have demonstrated the potential of and illuminated the issues associated with genome-wide monoclonal antibody generation.RIGHTS : This article is licensed under the BioMed Central licence at http://www.biomedcentral.com/about/license which is similar to the 'Creative Commons Attribution Licence'. In brief you may : copy, distribute, and display the work; make derivative works; or make commercial use of the work - under the following conditions: the original author must be given credit; for any reuse or distribution, it must be made clear to others what the license terms of this work are

    Search for Λc+pK+π\Lambda_c^+ \to p K^+ \pi^- and Ds+K+K+πD_s^+ \to K^+ K^+ \pi^- Using Genetic Programming Event Selection

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    We apply a genetic programming technique to search for the double Cabibbo suppressed decays Λc+pK+π\Lambda_c^+ \to p K^+ \pi^- and Ds+K+K+πD_s^+ \to K^+ K^+ \pi^-. We normalize these decays to their Cabibbo favored partners and find BR(\text{BR}(\Lambda_c^+ \to p K^+ \pi^-)/BR()/\text{BR}(\Lambda_c^+ \to p K^- \pi^+)=(0.05±0.26±0.02)) = (0.05 \pm 0.26 \pm 0.02)% and BR(\text{BR}(D_s^+ \to K^+ K^+ \pi^-)/BR()/\text{BR}(D_s^+ \to K^+ K^- \pi^+)=(0.52±0.17±0.11)) = (0.52\pm 0.17\pm 0.11)% where the first errors are statistical and the second are systematic. Expressed as 90% confidence levels (CL), we find <0.46< 0.46 % and <0.78 < 0.78% respectively. This is the first successful use of genetic programming in a high energy physics data analysis.Comment: 10 page

    Measurement of the D+ and Ds+ decays into K+K-K+

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    We present the first clear observation of the doubly Cabibbo suppressed decay D+ --> K-K+K+ and the first observation of the singly Cabibbo suppressed decay Ds+ --> K-K+K+. These signals have been obtained by analyzing the high statistics sample of photoproduced charm particles of the FOCUS(E831) experiment at Fermilab. We measure the following relative branching ratios: Gamma(D+ --> K-K+K+)/Gamma(D+ --> K-pi+pi+) = (9.49 +/- 2.17(statistical) +/- 0.22(systematic))x10^-4 and Gamma(Ds+ --> K-K+K+)/Gamma(Ds+ --> K-K+pi+) = (8.95 +/- 2.12(statistical) +2.24(syst.) -2.31(syst.))x10^-3.Comment: 10 pages, 8 figure

    A Non-parametric Approach to the D+ to K*0bar mu+ nu Form Factors

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    Using a large sample of D+ -> K- pi+ mu+ nu decays collected by the FOCUS photoproduction experiment at Fermilab, we present the first measurements of the helicity basis form factors free from the assumption of spectroscopic pole dominance. We also present the first information on the form factor that controls the s-wave interference discussed in a previous paper by the FOCUS collaboration. We find reasonable agreement with the usual assumption of spectroscopic pole dominance and measured form factor ratios.Comment: 14 pages, 5 figures, and 2 tables. We updated the previous version by changing some words, removing one plot, and adding two tables. These changes are mostly stylisti

    Measurements of Ξc+\Xi_c^{+} Branching Ratios

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    Using data collected by the fixed target Fermilab experiment FOCUS, we measure the branching ratios of the Cabibbo favored decays Ξc+Σ+Kπ+\Xi_c^+ \to \Sigma^+K^-\pi^+, Ξc+Σ+Kˉ(892)0\Xi_c^+ \to \Sigma^+ \bar{K}^{*}(892)^0, and Ξc+Λ0Kπ+π+\Xi_c^+ \to \Lambda^0K^-\pi^+\pi^+ relative to Ξc+Ξπ+π+\Xi_c^+ \to \Xi^-\pi^+\pi^+ to be 0.91±0.11±0.040.91\pm0.11\pm0.04, 0.78±0.16±0.060.78\pm0.16\pm0.06, and 0.28±0.06±0.060.28\pm0.06\pm0.06, respectively. We report the first observation of the Cabibbo suppressed decay Ξc+Σ+K+K\Xi_c^+ \to \Sigma^+K^+K^- and we measure the branching ratio relative to Ξc+Σ+Kπ+\Xi_c^+ \to \Sigma^+K^-\pi^+ to be 0.16±0.06±0.010.16\pm0.06\pm0.01. We also set 90% confidence level upper limits for Ξc+Σ+ϕ\Xi_c^+ \to \Sigma^+ \phi and Ξc+Ξ(1690)0(Σ+K)K+\Xi_c^+ \to \Xi^*(1690)^0(\Sigma^+ K^-) K^+ relative to Ξc+Σ+Kπ+\Xi_c^+ \to \Sigma^+K^-\pi^+ to be 0.12 and 0.05, respectively. We find an indication of the decays Ξc+ΩK+π+\Xi_c^+ \to \Omega^-K^{+}\pi^+ and Ξc+Σ(1385)+Kˉ0\Xi_c^+ \to \Sigma^{*}(1385)^+ \bar{K}^0 and set 90% confidence level upper limits for the branching ratios with respect to Ξc+Ξπ+π+\Xi_c^+ \to \Xi^-\pi^+\pi^+ to be 0.12 and 1.72, respectively. Finally, we determine the 90% C.L. upper limit for the resonant contribution Ξc+Ξ(1530)0π+\Xi_c^+ \to \Xi^{*}(1530)^0 \pi^+ relative to Ξc+Ξπ+π+\Xi_c^+ \to \Xi^-\pi^+\pi^+ to be 0.10.Comment: 14 pages, 8 figure
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