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Sample GSM937919 Query DataSets for GSM937919
Status Public on Jan 17, 2014
Title KO TSCs at d0, biological rep3
Sample type RNA
 
Source name trophoblast stem cells, Lsd1-deficient, d0
Organism Mus musculus
Characteristics strain: mixed C57Bl/6 and 129Sv
genotype: Lsd1-deficient
cell type: trophoblast stem cells (TSCs)
differentiation state: stemness state
time point: before induction of differentiation (d0)
Treatment protocol To induce differentiation, TSCs were cultured in TS medium in the absence of FGF4, heparin, and MEF-conditioned medium.
Growth protocol TSCs were cultured in the absence of primary mouse embryonic fibroblasts (MEFs) in medium supplemented with FGF4 (RD, 235-F4-025/CF, 30 ng/ml) and heparin (Sigma, H3149, 1.2 µg/ml). The medium contained 30 vol% TS medium (RPMI 1640, BD Biosciences, 354230), which includes 20% ES cell-qualified foetal bovine serum (Invitrogen), 1% penicillin-streptomycin (Lonza, DE17-602E), 1% glutamine (Lonza, BE17-605E), 1% sodium pyruvate (Invitrogen, 11360), 0.1 mM ß-mercaptoethanol and 70 vol% MEF-conditioned medium (collected from mitomycin C-treated (Sigma, M4287) MEFs cultured in TS medium).
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the Affymetrix ExpressKit protocol starting from 200 ng total RNA.
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45°C on GeneChip Mouse430_2. GeneChips were washed and stained in the Affymetrix Fluidics Station 450 using the Affymetrix Hybridization, Wash and Stain Kit.
Scan protocol Arrays were scanned in a GeneArray Scanner (Agilent).
Description F-d0+3_Mouse430_2
Data processing The data were RMA normalized using R/Bioconductor. The normalized data were analyzed with Genedata Analyst 7.0 (Box Plot; Principal Component Analysis; Hierarchical Clustering; N-Way ANOVA; T-Test).
 
Submission date May 25, 2012
Last update date Jan 17, 2014
Contact name Thomas Günther
E-mail(s) [email protected]
URL http://www.uniklinik-freiburg.de/molgyn/live/Persons-1/TG_en.html
Organization name Freiburg University Medical Center
Department Central Clinical Research
Street address Breisacherstr. 66
City Freiburg
ZIP/Postal code 79106
Country Germany
 
Platform ID GPL1261
Series (1)
GSE38277 Lsd1 coordinates trophoblast development by retaining stem cells in their niche and directing cell fate

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
1415670_at 1063.0381
1415671_at 2511.9824
1415672_at 3472.6255
1415673_at 559.8531
1415674_a_at 1023.7267
1415675_at 760.9871
1415676_a_at 4539.957
1415677_at 368.50406
1415678_at 2150.5295
1415679_at 2132.1187
1415680_at 1478.5297
1415681_at 1546.6676
1415682_at 553.2443
1415683_at 6250.335
1415684_at 459.2033
1415685_at 919.09814
1415686_at 914.337
1415687_a_at 6273.5557
1415688_at 1493.6166
1415689_s_at 589.63446

Total number of rows: 45101

Table truncated, full table size 926 Kbytes.




Supplementary file Size Download File type/resource
GSM937919_F-d0+3_Mouse430_2.CEL.gz 3.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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