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Various concentrations of model NaCl solutions were used to study the ohmic and non-ohmic resistances in the stack under different hydrodynamic conditions.
For systems with surface coverage and concentrations of model mucins mimicking physiological conditions, we determined the equilibrium distribution of inert nanoparticles within the mucus layers using an efficient replica exchange Monte Carlo sampling procedure.
The concentrations of model proteins in the mixture were prepared as follows: ribonuclease A, 0.05 mg/mL; trypsin inhibitor, 0.05 mg/mL; and carbonic anhydrase, 0.01 mg/mL.
In particular, if the "ON" fixed point falls onto the saturated regime of the nullcline intersections, then the steady state concentrations of model components, such as [NANOG] and [OCT4] may be differently altered.
GSA of the model of ER-dependent gene expression was performed according to the following algorithm: We perturbed all independent kinetic parameters of the model (dissociation and reaction rate constants) and total concentrations of model species, with the exception of the inhibitor concentration (It), whose value was fixed to a certain value during each run of GSA.
All processes of immune response are described as system of ordinary differential equations: d x dt = N ⋅ v, x 0 = x 0 Here, x = [x1,…,xm]T is vector of model variables concentrations, x 0 = [x10,…,xm0]T is vector of initial concentrations of model variables, v = [v1,…,vn]T is vector of reaction rates, N is stoichiometric matrix which has n columns and m rows.
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Initial concentration of model species and total protein amount.
The area under the curve was calculated and compared to the calibration curve to determine the concentration of model drug entrapped within the fibres.
The stickleback androgen bioassay can be adapted to detect antiandrogens in two ways: Simultaneous treatment of females with an androgen Photoperiodic manipulation of male stickleback reproductive status The degree of antagonism by a given compound depends on the following: Type and concentration of model androgen used (17α-MT being more potent than DHT).
Batch experiments were performed in triplicate in acid washed 120 mL serum bottles containing 100 mL of Cr VI) contaminated groundwater, or a known concentration of model Cr VI) solution (K2CrO4), using ultrapure water adjusted to pH 12 with 10 M NaOH.
The photocatalytic process was optimized with respect to the concentrations of the model substances during degradation.
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