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For hESCs, d0, and d5 of differentiation, biological triplicates were generated.
Biological triplicates were generated for each strain and expression values computed using the RMA implementation (default parameters) in the affy package from Bioconductor [ 54].
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2D-DIGE protein expression maps (PEMs) for the biological triplicate samples were generated for both temperature shifted and standard cultures for CHO-K1 cells at 72 hrs and 144 hrs.
The means from the biological triplicates were used in a 4 Parameter Logistic Model to generate an EC50 and Hill slope.
Biological triplicates were measured twice.
Biological triplicates were performed.
Biological triplicates were performed for each sample.
Biological triplicates were prepared for each strain.
Biological triplicates were run for each sample.
Biological triplicates were assayed for all conditions.
Technical and biological triplicates were performed.
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