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All analyses were conducted in triplicate to ensure accuracy and precision.
All experiments were conducted in triplicate to ensure reproducibility.
Each reaction was conducted in triplicate to ensure reproducibility of results.
Standard TaqMan qRT-PCR Gene Expression assays were conducted in triplicate to quantify HOXA9 expression levels relative to GUSB.
The experiments were conducted in triplicate to determine dose effect by mass and by number of fibers with aspect ratios greater than 3.
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Experiments were conducted in triplicates to check the reproducibility of SK production using optimized conditions.
Study was conducted in triplicates to avoid the manual error and details are shown in (Table 1).
In accordance with the NREL LAP [ 38], enzymatic hydrolysis was conducted in triplicate at a solids loading corresponding to 1% (w/w) glucan in 0.05 M citrate buffer (pH = 4.9) containing 10 mg/mL sodium azide in 50 mL Erlenmeyer flasks.
Note that the IC50 value for OV3133 R2) was based on one experiment conducted in triplicate due to the low clonogenic efficiency of OV3133 R2).
Reactions were conducted in triplicate and subjected to agarose gel electrophoresis and quantitative reverse transcriptase real-time PCR (Fig. 5).
Each reaction was conducted in triplicate and three to nine biological samples prepared independently were used in data analysis.
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