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In order to identify such pathways, these studies utilized a fixed collection of gene lists based on current biological knowledge.
Assays to test for rate-limiting diffusional encounter of O2 utilized a fixed CTAD788 826 concentration of 80 μM (∼ KM CTAD)) and saturating concentrations of FeSO4 (25 μM), αKG (100 μM), and ascorbate (2 mM), with the exception of the addition of sucrose (25% w/w) to the 50 mM HEPES, pH 7.00, to give a relative visocisty of η/η0 = 2.4.
In [17], the authors utilized a fixed point theorem of generalized concave operators to study problem (1.1) and established the existence and uniqueness of monotone positive solutions.
Thus, the analysis method differed across the samples; we utilized a fixed effect method for the overall sample and a random effect method for the subsample.
Assays with αKG as the varied substrate (from 2.5 to 100 μM) utilized a fixed CTAD concentration of 100 μM [∼ KM CTAD)] to conserve on the use of the peptide.
Steady-state assays in which O2 was the varied substrate (0.020 1 mM) utilized a fixed CTAD788 826 concentration of either 80 μM (∼ KM CTAD)) or 150 μM (∼2 KM CTAD)) and saturating concentrations of FeSO4 (25 μM), αKG (100 μM), and ascorbate (2 mM), prepared in 50 mM HEPES, pH 7.00.
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The conventional approaches utilize a fixed gain PI controller that increases the error between the reference and actual DC link voltage under sag condition.
Additional features on biosorption experiments utilizing a fixed bed column are also highlighted, as they offer useful information for biosorption process design.
Resonator stability was achieved with electrical and mechanical design utilizing a fixed position double coupling loop of novel geometry, thus minimizing the number of moving parts.
In contrast, Shan et al. [22] only utilize a fixed Gaussian kernel.
By utilizing a fixed pilot spacing of Δ k =2 as a result of the preamble structure, the STO estimation range is −T/4+T s ≤τ≤T/4−T s.
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