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Sample GSM509257 Query DataSets for GSM509257
Status Public on Jun 13, 2010
Title P4_Ovary_CTGF_biological rep1
Sample type RNA
 
Source name P4 Ovary incubated in the presence of 50 ng/ml CTGF for 48 hours
Organism Rattus norvegicus
Characteristics strain: Sprague-Dawley
gender: Female
tissue: ovary
developmental stage: day P4 incubated for 2 more days
Treatment protocol For each ovary sample from which RNA was collected for microarrays, 2-3 ovaries per well were cultured with media changes every 24 hours for two days in the absence (controls) or presence (treated) CTGF (human connective tissue growth factor)(50ng/mL, PeproTech Inc., NJ USA). Two or three ovaries from the same culture well (from different rat pups out of the same litter) and receiving the same treatment were pooled and homogenized together.
Growth protocol Four-day old female Sprague-Dawley rats (Harlan Laboratories, Inc., USA) were euthanized according to Washington State University IACUC approved protocols and the ovaries removed and cultured whole as described previously [Dole, G., et al., 2008].
Extracted molecule total RNA
Extraction protocol RNA was isolated from whole rat ovaries (2-3 ovaries per each sample) after homogenization in 1 ml Trizol™ reagent (Sigma-Aldritch, USA), according to manufacturer’s instructions.
Label biotin
Label protocol Biotin-labeled ssDNA were prepared according to the standard Affymetrix protocol from at least 300 ng total RNA (GeneChip® Whole Transcript (WT) Sense Target Labeling Assay Manual, 2005-2209, Affymetrix).
 
Hybridization protocol Following fragmentation, ssDNA were hybridized on Affymetrix Rat Gene 1.0 ST Array according to standard Affymetrix protocol. Chips were washed and stained in the Affymetrix Fluidics Station 4500.
Scan protocol GeneChips were scanned using Affymetrix GeneChip® Scanner 3000.
Description Gene expression data from rat P4 Ovary incubated in the presence of 50 ng/ml CTGF for 48 hours
Data processing The data were analyzed with Partek Genomic Suite 6.5 beta software (Partek Inc., St. Louis, MO) using RMA, GC-content adjusted algorithm background correction, quintile normalization, median polish methods for probesets summarization, and log values of probes signals using base 2.
 
Submission date Feb 13, 2010
Last update date Feb 16, 2010
Contact name Michael K Skinner
E-mail(s) skinner@mail.wsu.edu
Organization name WSU
Department SBS
Street address Abelson 507
City Pullman
State/province WA
ZIP/Postal code 99163
Country USA
 
Platform ID GPL6247
Series (1)
GSE20324 Gene Bionetwork Analysis of Ovarian Primordial Follicle Development

Data table header descriptions
ID_REF
VALUE log2 GC-RMA normalized signal intensity

Data table
ID_REF VALUE
10701620 6.47015
10701630 4.57002
10701632 4.13991
10701636 4.80988
10701643 5.5999
10701648 4.86015
10701654 8.86979
10701663 7.76023
10701666 6.35019
10701668 7.84025
10701671 5.36992
10701674 6.17013
10701679 7.51983
10701684 6.45985
10701689 9.04989
10701691 4.96984
10701697 5.89994
10701699 7.72
10701709 10.6597
10701714 4.78991

Total number of rows: 27342

Table truncated, full table size 448 Kbytes.




Supplementary file Size Download File type/resource
GSM509257.CEL.gz 4.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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