Exact(2)
Comparative treatment of the same solutions with a Pt anode yields a quite poor depollution because of the generation of much lower amounts of reactive OH on its surface.
For each value of ε and for each instance, the objective function of the solutions obtained by AD and ST with perturbed input data have been compared with the objective function values obtained by the same solutions with no perturbation on link travel times (i.e., with ε = 0 ).
Similar(57)
Thirteen days after germination, the plants received the same solution with or without humic acid (3.5 mM of C).
The crystals of Y122F and F86YF87Y were grown in the same solution with 0.02 mol/L adenosine-5'-triphosphate disodium salt hydrate added.
Steel samples were first prepassivated in saturated solution of Ca(OH 2 and then exposed to the same solution with 1% NaCl addition, simulating pore liquid in chloride contaminated concrete.
Regarding the optimization algorithms, since the optimization methods converge to the same solution, with different starting points and in a reasonable amount of time, the values assumed for the parameters could be considered correct.
The main result is that both design problems for the CSTR + PFR configuration have the same solution with respect to the optimal volume of the CSTR, which is given as an explicit function of the incoming substrate concentration, the volumetric flow rate and the coefficients of the Monod growth rate function.
After IEF, the strips were equilibrated in a solution containing 50 mmol · L−1 Tris-HCL, 6 mol · L−1 urea, 30% glycerol, 2% SDS, and 1% DTT for 15 min, and then an additional 15 min in the same solution with 2.5% iodoacetamide substituted for 1% DTT.
Based on the above discussion, we get the question: If the condition of mutually identically independent distribution is discarded, can one obtain the same solution with Theorem 1.1 from Y ∼ E n × m p ( μ ⋅ ( II m ′ ⊗ I p ), m Σ ) ?
For immunoblotting, membranes were blocked in PBS with 10% fat free milk and incubated in the same solution with primary antibody at room temperature for 1 hour.
The cell membranes were permeabilized in PBS containing 0.2% saponin and 5% goat serum for 20 min at RT. Cells were then stained at RT in the same solution with the antibodies as specified above.
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