Sentence examples for measuring mitochondrial activity from inspiring English sources

The sensitivity to cytokines in INS-1E and INS-1E-ZnT8-EGFP cells was estimated by measuring mitochondrial activity (figure 3).

Cell viability was determined by measuring mitochondrial activity using 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT), as previously described.

Cells were treated with increasing doses of either NVP-BEZ235 or GDC-0980, and viability and growth inhibition were assayed by measuring mitochondrial activity at 72 h using an MTT assay.

Cell viability was performed by measuring mitochondrial activity (mitochondrial dehydrogenase) in living cells using XTT (2,3-Bis- 2-methoxy-4-nitro-5-sulfophenyl]-2H-tetrazolium-5-carboxyanilide salt) (Sigma-Aldrich).

It measures mitochondrial activity through enzymatic reaction on the reduction of MTT to formazan [7].

While no decrease in viability was noted when using the MTT assay (Figure 6A), which measures mitochondrial activity, epithelial fracture was noted in 3 of 5 ectocervical and colorectal tissues cultured with tenofovir or vehicle control gels (Figure 6B).

Alamar Blue measures mitochondrial activity which is lost upon cell death.

To confirm this, we measured mitochondrial activity by high-resolution respirometry in whole flies using 30 day-old males.

We assessed cell viability using a tetrazolium dye assay (CCK-8, Dojindo Laboratories, Gaithersburg, MD) that measures mitochondrial activity.

Indeed the data from the MTT cell proliferation assay that measures mitochondrial activity showed no differences in cell viability and proliferation between control and MCF10A-NR4A1 cells.

To test this idea we measured mitochondrial activity inside of living cells using membrane-permeable dye JC-1 (reviewed by Perry et al., 2011).