Sentence examples for microarray analysis determined from inspiring English sources
Microarray analysis determined the alterations in the ovarian transcriptome that occurred in response to treatment of ovaries with AMH, FGF2, BMP4, GDNF, FGF7, KITL, LIF, and PDGFB.
Our microarray analysis determined that Ets-1 is a regulator of antioxidant gene expression in ovarian cancer cells, particularly glutathione peroxidases, which preferentially target H2O2 and lipid hydroperoxides for detoxification.
Microarray analysis determined that transcript levels of three monosaccharide transporters were significantly decreased at 8 DPA in mutant elongating fibers (Additional file 7).
Conversely antibody-based microarray analysis determined that doxorubicin-resistant MDA-MB-231 have decreased protein expression of p-ERK1, cyclin B1 and cyclin D2 [ 55].
Previous reports using microarray analysis determined that CENP-A mRNA levels were higher in oocytes and hESCs relative to somatic cells (27– 31).
Again, this is in accordance with the results of Ophir et al. [12], who by means of microarray analysis, determined that the genes that were more differentially expressed between genotypes in the brain, where NF-κB-regulated and showed that NF-κB activation was more pronounced in the microglia of apoE4 versus apoE3 mice.
The quality of the total RNA for microarray analysis was determined using UV spectrophotometer and Agilent 2100 Bioanalyzer and had an OD260/OD280 ratio ranging from 1.9 to 2.1.
Briefly, the quality of the total RNA for microarray analysis was determined using Spectra Max Plus (Molecular Devices) and had an OD260/OD280 ratio ranging from 1.9 to 2.1.
The expression of several genes significantly affected or related to processes affected by the two factors in the microarray analysis was determined by RT-qPCR (Table 3).
In this study, we investigated the gene data sets and pathways by microarray analysis and determined the effect on carcinoma cell phenotype by migration assays.
H. glycines gene expression from the microarray analysis was determined to correlate with that obtained from previous qRT-PCR analyses [ 46] (Table 6).
