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19 Incorporating fluorine labels allowed us to exploit the significant chemical shift dispersion and excellent sensitivity of F NMR spectroscopy to interrogate the composition of hydrazone-bound monolayers before and after dynamic covalent exchange reactions.
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Class scores, together with ground-truth labels, allow us to compute the AUC of a model, which is then averaged across folds according to cross validation.
Labels allow us all to make choices about what we serve our families and what sort of food system we support.
In this way, the labels allow us to specify any kind of additional information concerning the entities to which the formulas refer.
Furthermore, the iTRAQ labeling allowed us to identify 9 unique peptides of collagen II (COL2A1), a specific cartilage marker that was not previously detected using the MALDI-MS approach.
Isotope labeling allowed us to track the chemical changes that occurred to a specific set of Fe atoms, even as more Fe(II) was introduced to the reactor.
This labeling scheme, in conjunction with Alexa 488 phalloidin label, allowed us to investigate individual actin filaments as they entered into and exited from the dynamic contractile ring.
Moreover, mosaic labeling allowed us to visualize the precise IPL dendritic stratification patterns of single RGCs.
The label allowed us to conclusively determine that the compounds detected in the culture media were derived from the added substrate.
This combination of labelling allowed us to examine whether MyoD-stained nuclei were in a SC position or within the myofibre plasma membrane, or whether they belonged to another cell type (Fig. 2).
Embedded stereochemical labeling allows us to represent the relative stereoconfiguration of stereogenic centers.
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