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Exact(9)
The blood samples were run through a series of tests to look for patterns associated with something called the "conserved transcriptional response to adversity" or CTRA.
At least 10%% of the blood samples were run twice in separate assays with a concordance of genotype designation of 100%%.
The blood samples were run in duplicate.
For each hormone, all fetal blood samples were run in a single assay.
Diet samples were isotopically analyzed in duplicate, while blood samples were run in triplicate.
Similarly, blood samples were run across the remaining four chips with the same blood control sample run on each chip.
Similar(51)
A small set of samples from KS patients and a panel of 100 blood donor samples were run as ELISA positive and negative controls, respectively.
All reactions were performed in triplicate (0.5 μl of 20X TaqMan Gene Expression Assay, 5 μl of 2X TaqMan Gene Expression Master Mix, 2 ng blood cDNA or 1.5 ng dura cDNA, water to bring the reaction volume to 10 ul) and run on a ViiA™ 7 Real-Time PCR System (Applied Biosystems, Grand Island, NY); blood and dura samples were run on separate 384 well plates.
The negative control samples (genomic DNA from healthy blood donors and cell lines DNA samples) were run in at least 10 replicates.
Triplicate samples were run.
Samples were run in quadruplicate.
More suggestions(15)
blood samples were sampled
blood samples were taken
blood samples were collected
blood samples were drawn
blood samples were covered
blood samples were processed
blood samples were performed
blood samples were analysed
blood donors were run
blood spots were run
blood samples were obtained
blood samples were assessed
blood samples were assayed
blood samples were kept
blood samples were analyzed
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