66 research outputs found
Chromo-polarizability and pipi final state interaction
The chromo-polarizability of a quarkonium state is a measure of the amplitude
of the - chromo-electric interaction of the quarkonium with soft gluon
fields and can be measured in the heavy quarkonium decays. Based on the chiral
unitary approach, formulas with modification caused by the wave
final state interaction (FSI) for measuring the chromo-polarizabilities are
given. It is shown that the effect of the wave FSI is very
important in extracting chromo-polarizabilities from the experimental data. The
resultant values with the FSI are reduced to about 1/3 of those determined
without the FSI. The consequences of the FSI correction in the -nucleon
scattering near the threshold are also discussed. The estimated lower bound of
the total cross section is reduced from about 17 mb to 2.9 mb, which agrees
with the experimental data point and is compatible with the previously
estimated values in the literature. In order to understand the interaction of
heavy quarkonia with light hadrons at low energies better and to obtain the
chromo-polarizabilities of quarkonia accurately, more data should be
accumulated. This can be done in the decay at
BES-III and CLEO-c and in the decay at B
factories.Comment: 5 pages, 3 figures, ReVTeX4. Version accepted for publication in
Phys. Rev.
The role of in and reactions
The near threshold meson production in proton-proton and
collisions is studied with the assumption that the production mechanism is due
to the sub--threshold resonance. The , and
-meson exchanges for proton-proton collisions are considered. It is
shown that the contribution to the reaction from the t-channel
meson exchange is dominant. With a significant
coupling ( = 0.13), both and
data are very well reproduced. The significant coupling of
the resonance to is compatible with previous indications
of a large component in the quark wave function of the
resonance and may be the real origin of the significant enhancement of the
production over the naive OZI-rule predictions.Comment: 15 pages, 6 figure
On the structure of the pi pi invariant mass spectra of the Upsilon(4S)-->Upsilon(1S,2S) pi^+ pi^- decays
We perform a model-independent analysis for recently reported data of the
invariant mass spectra in the
decays and point out that there does
exist a broad peak below 0.6 GeV in the data of the
decay, which is analogous to that in
the decay. With the data of
decays, we further test our model developed for studying the
puzzle in the decay. The result shows
that with such a model, all the invariant mass spectra of
decays can be described. We also predict the
distributions of
decays, which can be used to justify
our model prediction.Comment: 11 pages, 5 figures. Extended to include new data; title changed.
Version accepted for publication in Phys. Lett.
Dynamically generated 0^+ heavy mesons in a heavy chiral unitary approach
In terms of the heavy chiral Lagrangian and the unitarized coupled-channel
scattering amplitude, interaction between the heavy meson and the light
pseudoscalar meson is studied. By looking for the pole of scattering matrix on
an appropriate Riemann sheet, a bound state with the mass of
GeV is found. This state can be associated as the narrow
state found recently. In the same way, a bound
state is found, and its mass of GeV is predicted.
The spectra of and with are further investigated. One
broad and one narrow states are predicted in both charm and bottom sectors. The
coupling constants and decay widths of the predicted states are also
calculated.Comment: 15 pages, 1 figure. One numerical error in Eq.16 correcte
Fluorescence detection of single nucleotide polymorphisms using a universal molecular beacon
We present a simple and novel assay—employing a universal molecular beacon (MB) in the presence of Hg2+—for the detection of single nucleotide polymorphisms (SNPs) based on Hg2+–DNA complexes inducing a conformational change in the MB. The MB (T7-MB) contains a 19-mer loop and a stem of a pair of seven thymidine (T) bases, a carboxyfluorescein (FAM) unit at the 5′-end, and a 4-([4-(dimethylamino)phenyl]azo)benzoic acid (DABCYL) unit at the 3′-end. Upon formation of Hg2+–T7-MB complexes through T–Hg2+–T bonding, the conformation of T7-MB changes from a random coil to a folded structure, leading to a decreased distance between the FAM and DABCYL units and, hence, increased efficiency of fluorescence resonance energy transfer (FRET) between the FAM and DABCYL units, resulting in decreased fluorescence intensity of the MB. In the presence of complementary DNA, double-stranded DNA complexes form (instead of the Hg2+–T7-MB complexes), with FRET between the FAM and DABCYL units occurring to a lesser extent than in the folded structure. Under the optimal conditions (20 nM T7-MB, 20 mM NaCl, 1.0 μM Hg2+, 5.0 mM phosphate buffer solution, pH 7.4), the linear plot of the fluorescence intensity against the concentration of perfectly matched DNA was linear over the range 2–30 nM (R2 = 0.991), with a limit of detection of 0.5 nM at a signal-to-noise ratio of 3. This new probe provides higher selectivity toward DNA than that exhibited by conventional MBs
Dynamically generated 1^+ heavy mesons
By using a heavy chiral unitary approach, we study the wave interactions
between heavy vector meson and light pseudoscalar meson. By searching for poles
of the unitary scattering amplitudes in the appropriate Riemann sheets, several
heavy states are found. In particular, a bound state with a mass
of GeV which should be associated with the recently observed
state is obtained. In the same way, a bound state
() with mass of GeV in the bottom sector is predicted.
The spectra of the dynamically generated and states in the
channel are also calculated. One broad state and one narrow state are found in
both the charmed and bottom sectors. The coupling constants and decay widths of
the predicted states are further investigated.Comment: 17 pages, 3 figures. Version accepted for publication in Phys. Lett.
Robust estimation of bacterial cell count from optical density
Optical density (OD) is widely used to estimate the density of cells in liquid culture, but cannot be compared between instruments without a standardized calibration protocol and is challenging to relate to actual cell count. We address this with an interlaboratory study comparing three simple, low-cost, and highly accessible OD calibration protocols across 244 laboratories, applied to eight strains of constitutive GFP-expressing E. coli. Based on our results, we recommend calibrating OD to estimated cell count using serial dilution of silica microspheres, which produces highly precise calibration (95.5% of residuals <1.2-fold), is easily assessed for quality control, also assesses instrument effective linear range, and can be combined with fluorescence calibration to obtain units of Molecules of Equivalent Fluorescein (MEFL) per cell, allowing direct comparison and data fusion with flow cytometry measurements: in our study, fluorescence per cell measurements showed only a 1.07-fold mean difference between plate reader and flow cytometry data
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