Sentence examples for molecules we chose from inspiring English sources

To test whether γδ T cells can recognize small molecules, we chose Cyanine 3 (Cy3) for analysis.

To test the generality of the observation that γδ T cells can recognize small molecules, we chose 4-hydroxy-3-nitrophenyl acetyl (NP) for analysis.

Because the interaction between rye and sss represents a connection to a known sleep-regulating gene, and two very different assays (genetic and electrophysiology) are consistent in indicating evolutionarily conserved repression of nAchRs by SSS-like molecules, we chose to leave these data in the manuscript.

Among these molecules we chose 407882 because of its water solubility, and used the following protocol: at Day 0 VTE was measured; next week, at Days 7 and 8, 20 µl of 10 µM 407882 was instilled into the nostrils of mice and VTE was measured again at Day 10.

Given that these are practically limitless (even if one might wish to start with 'core' molecules), we choose to be illustrative, and thereby provide a table of some of the kinds of reaction, reaction class or products for which the methods of DE have been used, with a slight focus on non-mainstream reactions.

In order to maximize boron content per molecule, we chose dendritic wedges built on a biocompatible scaffold that carries o-carboranes.

To adapt the assay to a nonradiometric format that was suitable for high-throughput screening of small-molecule libraries, we chose to measure ATP remaining at the end of the reaction using a luminescence readout (Kinase-Glo Plus; Promega).

Because long PCR can efficiently amplify regions of 10 kb or more at the single DNA molecule level, we chose 5-kb long insertion targets; if such a target acquired a full-length 6 kb L1 insertion, then the resulting 11-kb DNA fragment would still be amplifiable and could be subsequently purified by hybridization enrichment using L1 specific probes (Fig. 1B).

Although the model, as written, implies a simultaneous binding of n molecules of ligand, we chose it to absorb the combined uncertainties of choosing a single Kd2 to summarize the process and modeling the spectral perturbation of all ligands as equal in magnitude.

Because of difficulty in expressing a large ZO-1 molecule in E. coli, we chose a middle segment of ZO-1 based on our assessment of its proteolytic susceptibility to InhA (not shown).

To investigate the release kinetics of physiologically important molecules from the composite hydrogel, we chose two different growth factors and one cytokine: EGF, PlGF-1, and MCP-1 respectively, as example molecules conjugated to a fluorophore (either FITC, CFDA, or TAMRA) for detection purposes.