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Their viability can be determined by robots.
Finally, guidelines on viability can be self-fulfilling.
Accordingly, cell viability can be evaluated in a reproducible and sensitive manner by measuring the amount of ATP15.
Viability can be drastically reduced when directional bias in dispersal strength is higher than 25%.
95% cell viability can be achieved at the NPs concentration of 800 mg L−1 after 24 h of culture.
Results confirm that negative influence of the extreme pH fronts on the microbial viability can be prevented using this electro-bioremediation approach.
High viability can be achieved for human and porcine articular cartilage employing an 83% formulation, VS83, in combination with multiple addition/removal steps.
Insight into the importance of lamins to cellular viability can be gleaned from laminopathies, severe disorders caused by mutations in genes encoding lamins.
The effects of exposure to excitotoxins such as N-methyl-d-aspartate (NMDA) on cell viability can be determined by propidium iodide (PI) staining.
This increased cell viability can be explained by a nutrient effect [36, 37].
The expected increase in viability can be of one technology as in the example of genomic sequencing but could also include multiple technologies.
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