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Sample GSM398965 Query DataSets for GSM398965
Status Public on May 27, 2010
Title NT2_8D_R4
Sample type RNA
 
Source name Ntera2/D1 cells, 8 Day Retinoic Acid treated
Organism Homo sapiens
Characteristics cell type: Ntera2/D1
agent: Retinoic Acid
time: 8 Days
Biomaterial provider Stratagene, La Jolla, CA
Treatment protocol The cells were seeded at a density of 2 × 106 cells per T75 flask and treated with 10µM all-trans retinoic acid (RA, Sigma, Oakville, Ontario, Canada) in fresh medium every two days during a 28-day differentiation timecourse. Cells were harvested by tripsinization and centrifugation 0, 2, 4, 6, 8, 12, 14, 21, and 28 days following addition of RA. Time-course experiments were repeated several times to ensure multiple biological replicates for microarray analysis.
Growth protocol Human embryonal teratocarcinoma Ntera2/D1 (NT2) cells (Stratagene, La Jolla, CA) were cultured in high glucose Dulbecco’s modified Eagle’s medium (HG/DMEM, Invitrogen, Burlington, Ontario, Canada) supplemented with 10% fetal bovine serum (FBS, Wisent, Saint-Jean, Quebec, Canada).
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from the cells using TRI-Reagent (Molecular Research Center, Cincinnati, OH) according to the manufacturer’s instructions. High molecular-weight RNAs were removed by precipitation with 12.5% PEG-8000 and 1.25 M NaCl.
Label Cy3
Label protocol RNA labelling and hybridization to the microarrays was carried out using a method adapted from Thomson et al. 2004 (Thomson JM, Parker J, Perou CM, Hammond SM. 2004. A custom microarray platform for analysis of microRNA gene expression. Nat Methods 1: 47-53). Briefly, 10 or 25 µg total RNA was PEG-precipitated (as above), resuspended in 6 µl water, and mixed into a labelling reaction (final volume 10 µl) consisting of 500 ng 5’-phophate-cytidyl-uridyl-Cy3-3’ (Dharmacon, Chicago, IL), 10% DMSO, 0.1 mM ATP, 50 mM HEPES (pH 7.8), 3.5 mM DTT, 20 mM MgCl2, 0.1 µg BSA, and 20 U T4 RNA ligase (NEB, Ipswitch, MA). Reactions were incubated on ice in the dark for 2 hours before precipitation with 0.27 M sodium acetate, 20 µg glycogen, and 2.7 volumes ethanol in a 200 µl final volume. Following 10 min incubation on ice and 10 min centrifugation, the pellet was washed in 70% ethanol, centrifuged 5 min, briefly dried, and resuspended in 6 µl water.
 
Hybridization protocol Labelled RNA samples were hybridized to microarrays in a 35 µl final volume composed of 400 mM Na2HPO4 (pH 7.0), 5% SDS, 0.8% BSA, and 12% formamide. Hybridisation mixtures were denatured at 95°C for 4 minutes and immediately pipetted onto glass slides covered with 22×25 mm LifterSlips (Erie Scientific Company, Portsmouth, NH). Hybridizations were performed in custom-made sealed chambers submerged in a 37°C water bath overnight (18 hours). Slide washes were 3 min long: once in 2X SSC/0.025% SDS, three times in 0.8X SSC, and twice in cold 0.4X SSC. Immediately following the last wash, slides were dried by centrifugation.
Scan protocol Slides were scanned with a ScanArray 5000XL (Packard BioScience, Meriden, CT) confocal scanner at 10 µm resolution.
Description no additional information
Data processing Microarray scans were analysed with QuantArray software version 3.0 (Packard BioScience, Meriden, CT) using an adaptive quantitation method. Spots of poor quality on the arrays were flagged for removal from the data processing. Cy3 mean pixel intensities were background subtracted, log transformed, and replicate spots on the arrays were averaged. Microarray data were normalised between arrays using a standard median centering procedure. miRNAs were considered expressed if their normalised log2 hybridisation signal was ≥ 2. Differentially-expressed miRNAs were identified using a SAM (significance analysis of microarrays) threshold of 5% and a fold-change of 2.
 
Submission date Apr 29, 2009
Last update date May 27, 2010
Contact name Brandon Smith
E-mail(s) brandon.smith@nrc-cnrc.gc.ca
Organization name National Research Council Canada
Department Institute for Biological Sciences
Lab Neurogenesis and Brain Repair Group
Street address 1200 Montreal Road
City Ottawa
State/province Ontario
ZIP/Postal code K1A 0R6
Country Canada
 
Platform ID GPL8415
Series (1)
GSE15888 Large-Scale Expression Analysis Reveals Distinct microRNA Profiles at Different Stages of Human Neurodevelopment

Data table header descriptions
ID_REF
VALUE Median-centered, log2 signal intensity

Data table
ID_REF VALUE
b_let-7a -0.261004514
b_let-7b 0.929489415
b_let-7c -0.047808176
b_let-7d 0.208138134
b_let-7e -0.685744685
b_let-7f 0.261182701
b_let-7g -0.096055723
b_let-7i -0.253343922
b_miR-1 -0.23995233
b_miR-100 0.952314192
b_miR-103 1.015861506
b_miR-106b 2.074491255
b_miR-107 1.925910769
b_miR-10a 1.14216591
b_miR-122a 0.399336456
b_miR-124a 3.209739988
b_miR-125a 1.635524419
b_miR-125b 1.568110493
b_miR-126 -0.957701777
b_miR-126* -0.725722102

Total number of rows: 422

Table truncated, full table size 10 Kbytes.




Supplementary file Size Download File type/resource
GSM398965.txt.gz 106.8 Kb (ftp)(http) TXT
Processed data included within Sample table

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