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So far ENCODE has looked only at cells from one person for each of the cell types studied.
Each of the cell lines was successfully cryopreserved and thawed.
Representative measurements of TER were made in each of the cell lines used in these studies (via Ussing chamber).
In the second phase, each of the cell sites uses its channel estimates to design its own decoder.
In the second phase, each of the cell sites uses its channel estimates to design its own precoder.
In the third phase, each of the cell sites performs an equivalent channel sounding with either its designed precoder or left precoder.
LD50 value is given as μm of drug concentration as determined by WST-1 assay after 48h for each of the cell lines.
However, the content of these amino acids in each of the cell types was indistinguishable from controls when co-cultures were treated with MeHg.
100 µl Chloroform was added to each of the cell samples resuspended in trizol.
Therefore, we examined the importance of the different receptors by silencing them individually on each of the cell types.
Measurements were made in triplicate for each of the cell lines and the experiments were repeated three times.
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