We reevaluate the hadronic contributions to the muon magnetic anomaly, and to the running of the electromagnetic coupling constant at the Z-boson mass. We include new π + π − cross-section data from KLOE, all available multi-hadron data from BABAR, a reestimation of missing low-energy contributions using results on cross sections and process dynamics from BABAR, a reevaluation of all experimental contributions using the software package HVPTools together with a reanalysis of inter-experiment and inter-channel correlations, and a reevaluation of the continuum contributions from perturbative QCD at four loops. These improvements lead to a decrease in the hadronic contributions with respect to earlier evaluations. For the muon g − 2 we find lowest-order hadronic contributions of (692.3 ± 4.2) • 10 −10 and (701.5 ± 4.7) • 10 −10 for the e + e −based and τ-based analyses, respectively, and full Standard Model predictions that differ by 3.6σ and 2.4σ from the experimental value. For the e + e −-based five-quark hadronic contribution to α(M 2 Z) we find Δα (5) had (M 2 Z) = (274.9 ± 1.0) • 10 −4. The reduced electromagnetic coupling strength at M Z leads to an increase by 12 GeV in the central value of the Higgs boson mass obtained by the standard Gfitter fit to electroweak precision data.
Rolling circle amplification (RCA) is an isothermal enzymatic process where a short DNA or RNA primer is amplified to form a long single stranded DNA or RNA using a circular DNA template and special DNA or RNA polymerases. The RCA product is a concatemer containing tens to hundreds of tandem repeats that are complementary to the circular template. The power, simplicity, and versatility of the DNA amplification technique have made it an attractive tool for biomedical research and nanobiotechnology. Traditionally, RCA has been used to develop sensitive diagnostic methods for a variety of targets including nucleic acids (DNA, RNA), small molecules, proteins, and cells. RCA has also attracted significant attention in the field of nanotechnology and nanobiotechnology. The RCA-produced long, single-stranded DNA with repeating units has been used as template for the periodic assembly of nanospecies. Moreover, since RCA products can be tailor-designed by manipulating the circular template, RCA has been employed to generate complex DNA nanostructures such as DNA origami, nanotubes, nanoribbons and DNA based metamaterials. These functional RCA based nanotechnologies have been utilized for biodetection, drug delivery, designing bioelectronic circuits and bioseparation. In this review, we introduce the fundamental engineering principles used to design RCA nanotechnologies, discuss recently developed RCA-based diagnostics and bioanalytical tools, and summarize the use of RCA to construct multivalent molecular scaffolds and nanostructures for applications in biology, diagnostics and therapeutics.
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