The default d with the lowest priority min is converted into the following default rule which forms the root node of T: begin{aligned} mathrm{If},mathrm{{True},mathrm{then}},varvec{betaa }_{mathrm{default}} end{aligned} 2.
That is: The default d with the lowest priority min is converted into the following default rule which forms the root node of T: begin{aligned} mathrm{If},mathrm{{True},mathrm{then}},varvec{betaa }_{mathrm{default}} end{aligned}.
The ligand uptake, displayed in counts per minute (min), was converted to kilobecquerel (KBq) by defining a quantification factor using a fix amount of 111Indium in a water phantom as a reference.
ΔAbs min-1 was converted to U L-1 using an extinction coefficient of 11590 M-1cm-1.
Absorbance values were calculated as A265 (t) - A265 (t0), (t0 = 0 min); the values were converted in concentration of formed 5-FU, dividing absorbance values by 5-FU molar extinction coefficient at 265 nm (ε265).
RT was performed in a thermal cycler (Applied Biosystems, Foster City, CA): 25°C for 10 min, 42°C for 60 min, 99°C for 5 min, and 4°C for 5 min. All RNA samples were converted to cDNA together to minimize technical variability.
As the reaction time increased (around 50 min), the Ag crystals were converted to pentagonal 1-D structures, while the Ag nanoparticles completely disappeared.
The number of projections were 512 slices and total acquire time was around 4.27 min. All data were converted into digital imaging by TRIUMPH 'X-O' CT system software.
SPR spectra obtained from the reaction after (a) 5 min, (b) 15 min, (c) 25 min, (d) 35 min, and (e) 60 min (inset figures: the Ag nanostructures, at the initial reaction step, existed as Ag particles of 40 to 50 nm in diameter, and after 60 min, these Ag particles were converted into a 1-D structure approximately 30 nm in diameter).
Absorbance measurements were taken every 15 min. Absorbance values were converted to OD600 values using a standard curve of absorbance values of cultures at known OD600 taken on the same plate reader.
