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Sample GSM729412 Query DataSets for GSM729412
Status Public on Jul 01, 2011
Title Cbx2_KO_XX_1
Sample type RNA
 
Source name Cbx2_KO_XX gonads at E11.5
Organism Mus musculus
Characteristics genotype/variation: Cbx2_KO_XX
tissue: gonads
age: E11.5
Treatment protocol Embryos of the appropriate stage were manually selected under the dissecting scope. Four different genotypes of embryos at E11.5 (XY WT, XX WT, XY Cbx2 KO, and XX Cbx2 KO) were frozen in OCT compound (Sakura Finetechnical, Japan) without fixation. They were sectioned to 30 μm slices and stained with hematoxylin.The developing gonadal cells localized by GATA4 immunostaining and morphology were prepared using a Laser Microdissection System (Leica, Germany). The specimens prepared from two or three individuals were combined into one group, and three groups were prepared for each genotype.
Growth protocol Cbx2 KO embryos were generated by heterozygous mice for Cbx2 KO crossing. To stage the embryos accurately, tail somites were counted.
Extracted molecule total RNA
Extraction protocol RNeasy micro kit (QIAGEN) of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol Total RNAs (15 ng) prepared from these groups were subjected to two-cycle amplification and biotin labeling using MessageAmp™ II aRNA Amplification and MessageAmp™ II-Biotin Enhanced Kit (Ambion, USA), respectively.
 
Hybridization protocol Fifteen micrograms of labeled cRNA was fragmented and hybridized to the GeneChip® Mouse Genome 430 2.0 array according to the manufacturer’s instructions (Affymetrix, Santa Clara, CA, USA). GeneChips were washed with R-Phycoerythrin Streptavidin and The GeneChip Hybridization, Wash, and Stain Kit (Affymetrix).
Scan protocol GeneChips were scanned using the GeneChip Scanner 3000 (Affymetrix).
Description Initiation of sexually dimorphic transcription
Gene expression data from embryonic gonads at E11.5.
Data processing Obtained images files were analysed using Affymetrix data suite system, Expression Console (EC) version 1.1. The data were normalized with the RMA (Robust Multichip Average) normalization method in the R statistical package affy. The expression measure is calculated in log base 2 scale.
 
Submission date May 23, 2011
Last update date Jul 01, 2011
Contact name Yuko Katoh-Fukui
E-mail(s) [email protected]
Organization name National Inastitute for Longevity Sciences
Street address 35genngo ,moriokamachi
City Oobu
ZIP/Postal code 4748511
Country Japan
 
Platform ID GPL1261
Series (1)
GSE29485 Expression data from Mouse embryo

Data table header descriptions
ID_REF
VALUE RMA normalized

Data table
ID_REF VALUE
1415670_at 9.371447632
1415671_at 9.675244872
1415672_at 12.52349944
1415673_at 7.104951683
1415674_a_at 9.55358497
1415675_at 8.831196117
1415676_a_at 12.57564427
1415677_at 8.812583883
1415678_at 10.33059716
1415679_at 10.93813559
1415680_at 10.08764031
1415681_at 9.530895298
1415682_at 8.121914777
1415683_at 10.75507156
1415684_at 7.319789293
1415685_at 9.872922639
1415686_at 11.25975338
1415687_a_at 11.21565925
1415688_at 11.47359391
1415689_s_at 11.26616518

Total number of rows: 45101

Table truncated, full table size 1026 Kbytes.




Supplementary file Size Download File type/resource
GSM729412.CEL.gz 3.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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