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Sample GSM1349592 Query DataSets for GSM1349592
Status Public on Jun 01, 2014
Title REFA.1
Sample type RNA
Source name Reference Repeat 1
Organism Mus musculus
Characteristics tissue: Murine brain sample
Treatment protocol At each time point, follicles were pooled (for the microarray, 20-40 follicles per group, n = 3 independent experiments) and transferred into 1 ml of Liebovitz L-15 medium containing 10 U/ml alginate lyase (Sigma) for 20 min at 37°C to remove them from alginate. Follicles were aspirated, transferred into microcentrifuge tubes, flash frozen in liquid nitrogen, and stored at -80°C until RNA isolation was performed.
Growth protocol Multi-layered secondary follicles (150-180 µm in diameter) were mechanically isolated from ovaries of 16-day-old mice and individually encapsulated in alginate (FMC BioPolymers, Philadelphia, PA) as previously described (Kreeger et al. , 2006, West-Farrell et al., 2009, Xu et al. , 2006a). Alginate-encapsulated follicles were placed in individual wells of a 96-well plate containing 100 µl of growth medium (alpha minimum essential medium (alphaMEM) supplemented with 10 mIU/ml recombinant FSH (Organon, Roseland, NJ), 3 mg/ml bovine serum albumin (MP Biomedicals, Irvine, CA), 1 mg/ml bovine fetuin (Sigma, St. Louis, MO), 5 µg/ml insulin, 5 µg/ml transferrin, and 5 ng/ml selenium and cultured for 2, 4, 5, 6, or 8 days for microarray analysis. Half of the culture medium was exchanged every 2 days.
Extracted molecule total RNA
Extraction protocol RNA was purified from follicles using the Qiagen RNeasy Micro Kit according to the manufacturer’s protocol (Qiagen, Valencia, CA).
Label biotin
Label protocol mRNA samples were in vitro labeled using the TargetAmp 1-Round Aminoallyl-aRNA Kit (Epicentre, Madison, WI) a
Hybridization protocol randomly hybridized to BeadChips
Scan protocol Raw signal intensities of each probe were obtained using BeadStudio (Illumina).
Description TargetAmp 1-Round Aminoallyl-aRNA Kit
Data processing Statistical analyses were done in R (2008). Inadequate Illumina microarray probes due to misannotations or intronic coverage were removed from analysis using the Mouse WG V2.0 R0 file within ReMOAT ( (Barbosa-Morais et al. , 2010). Adequately annotated probes were considered to be above background if at least 2 of the 3 replicates measured were above background at P ≤ 0.01. The data were transformed using the variance stabilization transformation method (Lin et al. , 2008) and normalized by robust spline normalization (Du et al. , 2008).
Submission date Mar 17, 2014
Last update date Jun 01, 2014
Contact name and PhD
Organization name University of Chicago
Department Department of Surgery
Lab AB540
Street address 5841 South Maryland Avenue, MC 5032 Room AB540
City Chicago
State/province Illinois
ZIP/Postal code 60208
Country USA
Platform ID GPL6885
Series (1)
GSE55969 Dynamic study of In vitro murine follicle maturation in 3% alginate gels

Data table header descriptions
VALUE robust spline normalized signal
Detection Pval

Data table
ID_REF VALUE Detection Pval
ILMN_1212607 7.897912138 0.0689223
ILMN_1212612 11.04790687 0
ILMN_1212619 7.828583323 0.1829574
ILMN_1212628 7.774820437 0.4210526
ILMN_1212632 7.82195115 0.1967418
ILMN_1212636 10.35785494 0
ILMN_1212637 9.754955061 0
ILMN_1212645 7.744695294 0.7468672
ILMN_1212648 8.397995779 0
ILMN_1212653 8.391075599 0
ILMN_1212672 8.658721968 0
ILMN_1212682 7.913314061 0.05639098
ILMN_1212683 7.718601891 0.933584
ILMN_1212685 7.727265845 0.8909774
ILMN_1212692 7.784697254 0.3696742
ILMN_1212693 8.171278763 0.003759399
ILMN_1212695 7.80929876 0.235589
ILMN_1212698 7.735239185 0.8358396
ILMN_1212717 7.806718491 0.2506266
ILMN_1212720 8.525274315 0

Total number of rows: 23286

Table truncated, full table size 737 Kbytes.

Supplementary data files not provided
Raw data are available on Series record
Processed data included within Sample table

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