Participants from three organizations (CEA, IRSN and KIT) have addressed this transient using different system codes (CATHARE, DYN2B and ATHLET) and CFD codes (TRIO_U and OPEN FOAM).
Normalized Ca2+ transients were quantified from the area under each transient using Ionoptix analysis software.
The number of transients used was 16 and the relaxation delays were 2.0 s for DQF-COSY and 1.5 s for TOCSY.
Calculations are based on potential-dependent kinetic data derived from potentiostatic current transients using non-linear fit routines.
Each dataset was averaged over 32 transients using 32K time domain points.
To explore the possible role of intracellular Ca2+ homeostasis in obesity and/or aging-induced mechanical responses, we evaluated intracellular Ca2+ transients using the Fura-2 fluorescence measurement.
Linear time length images were converted into Ca2+ transients using ImageJ National Institutes of Healthh) and analysed using pCLAMP 10.3.
16 transients using 2.5 s relaxation delays were added with 2048 complex data.
For each t1, 96 transients using 1.5 s relaxation delay was added with 2048 complex data points.
Spectra were collected with 256 transients using an 8-second acquisition time and a 1-second recycle delay.
