Sentence examples for mixtures in Figure from inspiring English sources

Examination of the 32 aa mixtures in Figure 4 shows that all 8 mixtures with both tyrosine and cysteine also contained methionine.

Despite their structural similarity, templates T4, T5 and T6 have dramatically different effects on the palladium-catalyzed oxidative coupling of porphyrin dimer P2, as seen from the gel permeation chromatography (GPC) traces of crude reaction mixtures in Figure  1.

The cognate particle mixture in Figure 6a had a particle ratio of 1.5 1.0 (A′TYE/AFAM), a specific binding yield of 39.2%, and a binding selectivity ratio of 67.2 1.0 (positive/negative) compared to the noncognate control mixture that had a particle ratio of 1.5 1.0 (A′TYE/BFAM) and a specific binding yield of just 0.5%.

The fact that yields of Glc and Xyl were still increasing from 12 to 48 h, in some cases almost linearly (e.g., Spezyme CP and 11-component mixture in Figure 8a and Accellerase 1000 in Figure 8B), suggests that the enzymes were still active and that the plateau effect seen at 48 h in Figures 6c and 7c was not due to enzyme inactivation.

Annealing experiments, thus far, included a large excess of Pif1 relative to DNA, similar to that present in the unwinding reaction mixtures shown in Figure 1 that initially indicated that annealing might be occurring.

An initial SiO2 dielectric layer approximately 700-nm thick was deposited by high-density plasma chemical vapor deposition (HDP CVD), and the nanowires were exposed by a wet etching process using an ammonium fluoride mixture (shown in Figure 2b).

The mixture shown in Figure 9 originally contained approximately 31% reduced rTHB1.

Namely, it is easily seen that the tails of the two components of the mixture distribution in Figure 1 are heavier than a Gaussian distribution.

The rapid kinetics of noise in the AII inputs at 500 R*/rod/s matched the kinetics of noise in the presence of the mGluR6 agonist/antagonist mixture introduced in Figure 5 (FWHM of the autocorrelation function was 3.7 ± 0.3 ms in steady light vs 4.3 ± 0.3 ms in drugs, light n = 5, drugs n = 4; Figure 6F).

Experimental CMT values for some binary mixtures are shown in (Figure 9) along with the ideal mixing.

Connected TATI systems could be generated simply through the addition of both catalysts to the same mixture, as shown in Figure 3. Mixing imine 1 with benzylamine A1, ZnBr2, and base C1 in MeCN, in the presence of 3 Å MS, led to the generation of four imines, as evidenced by both H NMR spectroscopy and GC/FID analysis.