Exact(6)
Two replicates of each experiment were performed using different microarray slides, in which sample and control RNA, labeled either with Alexa Fluor 555 or Alexa Fluor 647 fluorochromes, were crossed in both combinations (dye-swapping procedure).
Complementary studies to the loss-of-function experiment were performed using a novel technology to introduce a constitutively active EGFR into the NSPs.
qRT-PCR analyses for the second animal experiment were performed using individual RNA samples for target genes Cpt1a and Acacb, as described above.
However, yield calculations for each experiment were performed using the composition of the individual batch of DAICS used for that experiment.
All sessions of the experiment were performed using a 14.0″ widescreen laptop (Lenovo T420; Lenovo, Morrisville, North Carolina, USA) running a resolution of 1600 × 900 on the Windows 7 operating system.
The experiment were performed using a protein interaction confidence minimum threshold of 3 star and above (i.e., reliability score of >0.75) and retrieved drug p-value at a minimum threshold of 0.05.
Similar(54)
A quantitative comparison experiment was performed using SDE/GC MS.
The second experiment was performed using three robots without obstacle.
This experiment was performed using several different face recognition algorithms.
This experiment was performed using a motion capture system.
The microdialysis experiment was performed using awake mice.
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