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Additional studies using this assay to measure the local cytokine tissue responses may help in defining a protective cytokine response and would be useful for the targeted design of efficacious vaccines, not only for PRRSV, but also for other swine pathogens.
Anticancer activity was determined using this assay to measure cell viability [ 28].
Industry is now very interested in using this assay to pre-screen and design trials.
There are several challenges when using this assay to measure the activity of a specific CPI within a biofluid sample, such as CSF.
We also tested the feasibility of using this assay to detect influenza (H5) viruses in clinical specimens from a patient with influenza (H5).
We are now using this assay to determine thymic function in the autoimmune disease systemic lupus erythematosus to test our hypothesis that a defect in thymic function contributes to lupus pathogenesis.
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The rapid removal of surface label with TCEP led us to use this assay to quantify uptake of labeled receptor over time.
We used this assay to study sensitivity difference towards H2O2 between different prxs in different subcellular compartments simultaneously (Cao et al. 2014).
We have used this assay to screen novel molecules in KM12 cells and to study pharmacodynamic properties of compounds in TRKA signaling.
We used this assay to screen 1040 compounds from two commercial compound libraries, and identified 17 that promoted differentiation, as well as 5 that promoted survival of hESCs.
We have used this assay to measure the ADCC activity of a humanized IgG1 antibody directed against the human CD20 antigen.
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