NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM887789 Query DataSets for GSM887789
Status Public on Jun 24, 2013
Title WTG4_Flk1_long_DexPlus_12h_rep1
Sample type RNA
 
Source name Flk1+/Ecad- mesoderm cells derived from mouse wild-type Gata4GR (WTG4) ES cells, +Dex, 12hr, replicate 1
Organism Mus musculus
Characteristics cell line: Line J1G4.211
genotype/variation: wild-type, stably expressing Gata4-glucocorticoid receptor ligand binding domain fusion gene
cell type: Flk1+/Ecad- mesoderm cells derived from embryonic stem (ES) cells, with further culture
dexamethasone: yes
time: 12h
Treatment protocol The cells were collected using 0.25% trypsin-EDTA, and single cell suspensions were stained using APC-conjugated anti-Flk1, biotinylated anti-E-cadherin (Eccd2, Takara Bio or DECMA-1, eBioscience) antibodies, and PE-conjugated streptavidin. Flk1 positive/E-cadherin negative cells were sorted by FACS-Aria (BD Biosciences). The cells were further cultured on type IV collagen-coated dishes in the differentiation medium (alpha-MEM supplemented with 10% FCS and 50 uM 2-mercaptoethanol) for 12 hours in the presence of 100 nM dexamethasone.
Growth protocol ES cells were plated onto a 10-cm dish with confluent OP9 stromal cells in the differentiation medium (alpha-MEM supplemented with 10% FCS and 50 uM 2-mercaptoethanol) for 4 days.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated by using the QIAshredder and the RNeasy Plus Micro Kit with gDNA Eliminator column (Qiagen) according to the manufacturer's protocols. RNA was quantified and quality controlled using the NanoDrop ND-1000 Spectrophotometer (Thermo) and the 2100 Bioanalyzer (Agilent).
Label Cy3
Label protocol Amplification and Cy3 labeling of RNA was prepared from 50 ng of RNA using the Low Input Quick Amp Labeling kit (Agilent) according to the manufacturer's instructions (G4140-90040 One-Color Microarray-Based Gene Expression Analysis Protocol Version 6.5). Purification of Cy3-labeled cRNA was performed using the RNeasy Mini Kit (Qiagen). Quantity, quality and dye incorporation of Cy3-labeled cRNA were checked using the NanoDrop ND-1000 Spectrophotometer (Thermo) and the 2100 Bioanalyzer (Agilent).
 
Hybridization protocol 600 ng of Cy3-labeled cRNA was hybridized in Agilent hybridization chambers for 17 hours at 65 degrees C and 10 rpm according to the manufacturer's instructions (G4140-90040 One-Color Microarray-Based Gene Expression Analysis Protocol Version 6.5).
Scan protocol Slide scanning was performed using the Agilent DNA Microarray Scanner G2505C with 3 um resolution and 20-bit dynamic range.
Description Gene expression data from Flk1+/Ecad- mesoderm cells derived from wild-type Gata4GR ES cells, with further 12hr-culture in the presence of dexamethasone to activate Gata4GR transgene
'short' sample represents short time course experiment (0-3h). In this experiment, dexamethasone was added before FACS sorting.
'long' sample represents long time course experiment (0-72h). In this experiment, dexamethasone was added after FACS sorting.
Data processing The scanned images were processed with Feature Extraction Software 10.7.3.1 (Agilent) using default parameters (protocol GE1_107_Sep09 and Grid 028005_D_F_20110406) to generate background subtracted and spatially detrended green Processed Signal intensities. Normalize signal intensities were obtained by a) removal of data of control probes, b) log2 transformation, and c) quantile normalization, which was performed using the normalizeQuantiles function of the limma package of the R.
 
Submission date Mar 06, 2012
Last update date Jun 24, 2013
Contact name Yuichi Kumaki
E-mail(s) kuma@cdb.riken.jp
Organization name RIKEN
Department Center for Developmental Biology
Street address 2-2-3 Minatojima-minamimachi, Chuo-ku
City Kobe
ZIP/Postal code 650-0047
Country Japan
 
Platform ID GPL13912
Series (1)
GSE36313 DNA Methylation Restricts Lineage-Specific Functions of Transcription Factor Gata4 during Embryonic Stem Cell Differentiation

Data table header descriptions
ID_REF
VALUE Quantile normalized log2 signal

Data table
ID_REF VALUE
1 null
2 null
3 null
4 2.88958
5 5.45366
6 1.76112
7 1.78986
8 10.2049
9 1.8569
10 1.87334
11 4.90052
12 1.89753
13 7.34534
14 11.8087
15 2.882
16 1.92946
17 11.5989
18 6.77996
19 10.946
20 15.7128

Total number of rows: 62976

Table truncated, full table size 832 Kbytes.




Supplementary file Size Download File type/resource
GSM887789_DKOG4_038_US91403665_252800511273_S01_GE1_107_Sep09_2_4.txt.gz 11.8 Mb (ftp)(http) TXT
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap