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(B ) Wells that showed statistically similar average ERK activation (cyan) to the control well (blue, 10 μM ATP) were selected for analysis (blue *, p-value >0.05, t-test).
The culture medium was added into the control well.
kern-0pt} { 100 - left( {text{spontaneous apoptosis in the control well}} right)}} (Fulda et al. 1997).
Check shots from the control well were used to create a velocity model from which the time to depth conversion was made.
The cell viability was obtained by comparing the absorbance of cells cultured on the nanofiber scaffolds to that of the control well containing DMSO.
R is the optical density of the control well, and n is the total number of the sole carbon substrates (ECO plates n = 31).
Similar(9)
The control wells contained medium supplemented with 2% DMSO.
The empty nanoparticles of similar dilutions were added to the control wells.
The control wells were added with ultrapure water without polycationic micelles.
The cell survival rate in the control wells without the PFC/ICG nanoemulsions was considered 100% cell survival.
The cell viability was calculated as follows: viability = (absorbance of the treated wells) / (absorbance of the control wells).
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CEO of Professional Science Editing for Scientists @ prosciediting.com