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DCs and macrophages were infected in duplicate with BCG and PD-L1 expression was assessed by flow cytometry.
Evaluation was carried out in duplicate, with samples grouped by taste type; 1 evaluation session per taste per replicate.
All experiments were done in duplicate with independently grown cells.
Tests were done in duplicate, with triplicate samples each time.
All experiments were performed in duplicate with four replicates for each treatment.
In this experiment, the wells were seeded in duplicate with 13 × 103 cells/cm2.
All the experiments were performed in duplicate, with the average value reported.
Analysis was performed in duplicate, with no-template controls.
Each experiment was performed in duplicate with identical results.
All reactions were run in duplicate with no template control.
Measurements were performed in duplicate with 0.5 µl cDNA.
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