Sentence examples for monitoring proteins for from inspiring English sources

Our results provide useful information on unique monitoring proteins for assessing the pathophysiological processes occurring before and after surgery for CAS.

These results indicated that antithrombin-III and zinc- α-2-glycoprotein would become unique monitoring proteins for evaluating the biological responses occurring before and after surgery for CAS.

We propose that antithrombin-III and zinc- α-2-glycoprotein are unique monitoring proteins for evaluating the pathophysiological and biochemical processes occurring before and after surgery for CAS.

The results indicated that antithrombin-III and zinc- α-2-glycoprotein would become unique monitoring proteins for evaluating pathophysiological and biochemical processes occurring before and after surgery for CAS.

Importantly, as expected, antithrombin-III (SERPINC1) and zinc- α-2-glycoprotein (AZGP1), possible monitoring proteins for surgery for CAS, were not included in the proteins that are differentially expressed in presurgical and postsurgical sera of AAA and TAA patients but were unique to those for CAS patients.

The results indicated that since the levels of antithrombin-III and zinc- α-2-glycoprotein in postsurgical sera did not return to levels similar to those in control sera, these two proteins are not candidates of disease markers for CAS but that they would become unique monitoring proteins for evaluating the pathophysiological and biochemical processes occurring before and after surgery for CAS.

Proteomics, aiming at the large-scale protein analysis in biological samples, is useful for monitoring proteins that are involved in physiological changes in cells or organisms [ 1].

We have previously shown that a peptide construct of the cytosolic sequence of human LAMP2A is useful as a tool for monitoring proteins interacting with this sequence.

On the basis of this empirical relationship, ESI-MS has been used as a tool for monitoring protein conformational changes in solution [ 146], including for protein footprinting experiments [ 147] (see " Protein surface mapping"), where oxidative modifications affect the solution-phase structure.

It is expected to have many potential applications in protein engineering and research, which include fluorescent labeling for monitoring protein folding, location, and trafficking in cells, and biotinylation for protein immobilization on streptavidin-coated surfaces including protein microchips.

Although in this study we implement the procedure for monitoring protein synthesis in C. elegans, the method can be readily adapted for applications in diverse organisms.