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RNA microarrays were conducted to identify global and specific gene expression changes.
Microarrays were conducted on bovine AC, AF and NP cells, using Affymetrix Genechip® Bovine Genome Arrays.
Six Agilent microarrays were conducted and plasma microRNA profiles were compared for each sample.
Microarrays were conducted at day 23 and day 10 of differentiation for hESC-Chol and HepaRG-Chol, respectively, and compared to hESC-HB and HepaRG-HB.
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Hybridization to the microarrays was conducted for 16 h at 45°C.
Fabrication of microarrays was conducted concurrently with EST sequencing, and we have sequenced 1,546 high-quality clones on the array to date.
The 70-mer oligonucleotides were synthesised by metabion international AG (Martinsried, Germany) and spotting of microarrays was conducted with a spot distance of 225 μm by Scienion AG (Berlin, Germany) using a sciFLEXARRAYER S11 piezo dispenser.
In this study, genome-wide expression profiling using cDNA microarrays was conducted for resistant Hofer and susceptible Trout Lodge rainbow trout strains following pathogen exposure with the primary objective of identifying specific genes implicated in whirling disease resistance.
The first study to carry out QTL analysis across genome-wide gene expression microarrays was conducted using an experimental cross between two strains of the yeast Saccharomyces cerevisiae (Brem et al. 2002).
RNA extraction, labeling, and hybridization for microarray were conducted using infested Kavya with GMB4M and uninfested plants as a control.
cDNA labeling, purification and hybridization against the microarray were conducted as previously described [ 25].
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