Exact(2)
It can be concluded that a proper concentration of alternative additive could be used to effectively achieve PG 76-22 binders.
Therefore, in addition to comparing GSH levels between morphs, we also compared the concentration of alternative antioxidants, as estimated by the levels of uric acid and total antioxidant capacity of plasma, and also oxidative damage, as estimated by the level of lipid peroxidation in erythrocytes.
Similar(58)
The concentrations of alternative carbohydrates and nitrogenous compounds were equivalent to the concentrations of carbon and nitrogen resources in the initial medium (12 g/L tryptone; 4 g/L glycerol).
Hence, higher concentrations of alternative buffers may be required, even at an ideal pKa.
For kinetic measurements involving varying concentrations of alternative carboxyacyl-CoA substrates, solution 1 contained the ACP, α-KGDH, NAD+, TPP, and α-ketoglutarate at four times their final concentrations, solution 2 contained the carboxyacyl-CoA substrate prepared at four times its final concentration, and solution 3 contained the AT prepared at twice its final concentration.
For kinetic measurements involving varying concentrations of alternative ACP substrates, solution 1 contained the carboxyacyl-CoA substrate, α-KGDH, NAD+, TPP, and α-ketoglutarate at four times their final concentrations, solution 2 contained the ACP prepared at four times its final concentration, and solution 3 contained the AT domain prepared at twice its final concentration.
To compare uptake of different N forms 200 ml of solutions containing 15N-labelled ammonium, glycine or nitrate (98 atom%) were added to each plant with the equimolar concentration of the alternative N forms supplied as unlabelled ammonium, glycine and nitrate.
We chose 10 mM CaCl2 as the concentration of this alternative divalent (here, the sign) because this quantity is known to enhance folding of the wild-type Tetrahymena ribozyme in the presence or absence of MgCl2 [ 8] and is also the concentration at which the PV ribozyme was selected for activity in the absence of MgCl2 [ 12].
Also in 2003, Wang et al. designed an algorithm that aimed to deconvolute the absolute concentrations of each alternative transcript present in a complex mixture starting from the hybridization intensities detected on splice chips [ 19].
For both the logistic regression analyses of apparent prevalence and the truncated Weibull models of concentration, plausible alternative models of apparent prevalence and concentration with various formulations were fitted and compared by calculating their Akaike Information Criterion (AIC) values.
They particularly act as concentration-dependent modulators of alternative RNA splicing, often in competition with other RNA-binding proteins, such as hnRNPs (Chen and Manley 2009).
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