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Healing efficiency was assessed using long-groove tapered double cantilever beam (TDCB) test samples, with embedded SMA wires across the crack plane.
Target processing efficiency was assessed using measures of workload resilience.
Clonal efficiency was assessed using a limiting dilution assay.
Amplification efficiency was assessed using LinRegPCR [ 16].
First, transduction efficiency was assessed using vectors expressing luciferase.
Transfection efficiency was assessed using qPCR and western blot.
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Main and interactive effects of three independent factors including pH (5 9), superficial gas velocity (0.05 0.15 cm/s) and time (20 60 min) on the removal efficiency were assessed using central composite face-centered design and response surface method (RS M.
The retrieval efficiency is assessed using a centroid data set (Figure 6, ISB data set).
Cy3 labeling efficiency and amplification efficiency were assessed using a NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies).
Quantity and quality of RNA and labeling efficiency were assessed using Nanodrop spectrophotometer and Bioanalyzer® (Agilent).
Coagulation, acid-base status, calcium balance and dialysis efficiency were assessed using standard biochemical markers.
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