In Tenon hospital, PCT concentrations were analyzed using a sandwich immunoassay based on time-resolved amplified cryptate emission (TRACE) measurement (Kryptor analyzer; B.R.A.H.M.S. Thermo Fischer, Germany).
The present study investigates the feasibility of the noise prediction for high-lift devices based on time-resolved particle image velocimetry (PIV).
The Kryptor Compact Plus was an IMA system, based on time-resolved amplified cryptate emission technology (TRACE), which measured the signal emitted from an immunocomplex with a time delay.
It automatically generates a system of differential equations modelling structure and dynamics of the network based on time-resolved gene expression data.
Recently, we established a non-optical method based on time-resolved impedance recordings to detect the collective behavior of a small ensemble of D. discoideum cells during the aggregation phase., The method referred to as electric cell-substrate impedance sensing (ECIS) essentially measures the dielectric characteristics of the cell bodies in contact with the electrode.
A two-probe tandem DNA hybridization assay was designed for the detection of Enterobacter cloacae based on time-resolved fluorescence.
For this purpose, we developed a simple and highly sensitive assay for β-(1→4 -galactosyltransferase (β4GalT) activity, which is based on time-resolved fluorometry of europium.
Therefore in order to gain additional information such as diffusion coefficients of gases in ionic liquids, we established an efficient and easily assembled set-up based on time-resolved FTIR measurements.
Based on time-resolved electroluminescence (TREL) measurement, more efficient carrier injection, transport, relaxation, and recombination associated with a stronger carrier localization and a low polarization effect in a nonpolar m-plane InGaN/GaN light emitting diode (m-LED), compared with those in a polar c-LED, are reported.
The assay is based on time-resolved measurements of the luminescence kinetics and implements multiple enzymes to convert PPi to ATP that is, in turn, utilized to produce light and to hydrolyze PPi for measurement of the steady state background luminescence.
