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Sample GSM1065339 Query DataSets for GSM1065339
Status Public on Jan 17, 2013
Title PGC_E16_F3-Vinclozolin_biological rep2
Sample type RNA
 
Source name Primordial germ cell from E16 days old F3 vinclozolin lineage rat embryo
Organism Rattus norvegicus
Characteristics treatment: F3 vinclozolin lineage
cell preparation date batch: 2
genetic background: Sprague-Dawley rat
gender: Male
cell type: Primordial germ cell
developmental stage: E16
Treatment protocol Gestating outbred Sprague-Dawley mother rats were given intraperitoneal injections of Vinclozolin (100mg/kg/day) or vehicle (DMSO, Control) from embryonic day 8-14 (E8-E14) of gestation (i.e. F0 generation) [Cupp AS, et al., 2003]. Subsequent F2 and F3 generations wee obtained from F1 rats.
Growth protocol Primordial germ cell were isolated from male embryos age E13 and E16 of F3 generation of vinclozolin and control lineages rats as described before [. Kafri T, Ariel M, Brandeis M, Shemer R, Urven L, et al. (1992) Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line. Genes Dev 6: 705-714.]. Male sex of gonads was confirmed by PCR for male specific SRY gene.
Extracted molecule total RNA
Extraction protocol RNA was isolated from primordial germ cells after lysis 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 Male gonads from embryonic day E16 rat
Gene expression data from embryonic day E16 male gonads of F3 vinclozolin lineage rat
For each mRNA microarray replica, PGC from 7-20 different male embryos were combined.
Data processing The data were analyzed with Partek Genomic Suite 6.6 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. Cell preparation date batch effect was removed.
 
Submission date Jan 16, 2013
Last update date Jan 17, 2013
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 (2)
GSE43559 Environmentally Induced Transgenerational Epigenetic Reprogramming of Primordial Germ Cells and Subsequent Germline [Affymetrix]
GSE59511 Environmentally Induced Transgenerational Epigenetic Reprogramming of Primordial Germ Cells and Subsequent Germline

Data table header descriptions
ID_REF
VALUE RMA, GC-content adjusted algorithm pre-processed signal values logarithms, base 2, cell prep date batch effect removed

Data table
ID_REF VALUE
10701620 6.04938
10701630 5.6262
10701632 4.58958
10701636 5.6557
10701643 5.63108
10701648 5.91284
10701654 6.14904
10701663 7.67595
10701666 8.13314
10701668 7.38516
10701671 5.31659
10701674 5.9499
10701679 6.20149
10701684 6.64567
10701689 10.6582
10701691 5.27073
10701697 7.71945
10701699 8.33479
10701709 9.87331
10701714 5.72992

Total number of rows: 27342

Table truncated, full table size 450 Kbytes.




Supplementary file Size Download File type/resource
GSM1065339_Marina-PGC_E16-Vin-2-072711-12.CEL.gz 4.7 Mb (ftp)(http) CEL
Processed data included within Sample table

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