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Sample GSM629745 Query DataSets for GSM629745
Status Public on Mar 04, 2011
Title P0_Ovary_AMH_biological rep 2
Sample type RNA
 
Source name P0 Ovary incubated in the presence of 50 ng/ml AMH for 24 hours
Organism Rattus norvegicus
Characteristics strain: Sprague-Dawley
gender: Female
tissue: ovary
organ culture date batch: 2
developmental stage: day P0
agent: AMH
Treatment protocol For each ovary sample from which RNA was collected for microarrays, 1-3 ovaries per filter/well were cultured for 24 hours in the absence (controls) or presence (treated) AMH (human Anti-Mullerian Hormone)(50 ng/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 Zero-day old (< 8 hour 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 450.
Scan protocol GeneChips were scanned using Affymetrix GeneChip® Scanner 3000.
Description Gene expression data from rat P0 Ovary incubated in the presence of 50 ng/ml AMH for 24 hours
Marina-PO-Ovary-AMH-2_6-052710-5.CEL
Data processing The data were analyzed with Partek Genomic Suite 6.5 beta software (Partek Inc., St. Louis, MO) on 6.21.2010, using RMA, GC-content adjusted algorithm background correction, quantile normalization, median polish methods for probesets summarization, and log values of probes signals using base 2. Organ culture date batch effect was removed.
 
Submission date Nov 28, 2010
Last update date Mar 04, 2011
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)
GSE25629 Inhibitory Actions of Anti-Müllerian Hormone (AMH) on Ovarian Primordial Follicle Assembly

Data table header descriptions
ID_REF
VALUE Logarithm of signal values, base 2, pre-processed with RMA, GC-content adjusted algorithm, organ culture date batch effect removed

Data table
ID_REF VALUE
10881964 4.80
10718673 4.33
10829622 4.48
10835501 8.93
10761688 8.59
10916822 4.06
10704882 4.99
10765335 7.69
10915578 7.28
10712171 9.33
10838437 4.37
10799578 5.03
10795203 10.81
10745470 3.72
10733829 7.09
10930347 6.55
10788101 8.76
10804960 4.28
10933457 8.28
10713316 7.98

Total number of rows: 27342

Table truncated, full table size 375 Kbytes.




Supplementary file Size Download File type/resource
GSM629745.CEL.gz 4.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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