|
Status |
Public on Jul 15, 2019 |
Title |
TS cells treated with DES replicate 3 |
Sample type |
SRA |
|
|
Source name |
TS cells treated with DES
|
Organism |
Mus musculus |
Characteristics |
cell line: F4 cell type: Trophoblast stem cells (TSCs) treatment: 20 μM diethylstilbestrol (DES, Esrrb inhibitor)
|
Treatment protocol |
1.6 x 10^5 TS cells were grown in 6-well plates for 2 days in 70CM + F4H medium in the presence of DES (20 μM) or the vehicle (ethanol)
|
Growth protocol |
TS cells were maintained in RPMI1640 (Sigma) supplemented with 20% FBS (Life Technologies), 1mM sodium pyruvate (Life Technologies), 50U/ml penicillin, 50μg/ml streptomycin, 100mM 2-mercaptoethanol (Sigma), 2mM Glutamax (Life Technologies), 25ng/ml FGF4 (R & D Systems), and 1μg/ml heparin (Sigma), with 70% of the media preconditioned by mitotically inactivated E12.5 embryonic fibroblasts (70CM + F4H medium)
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted from TS cells treated with DES or vehicle (ethanol) for 2 days using TRIzol reagent with PureLink RNA Micro Kit Single-end 100bp RNA-sequencing libraries were prepared using TruSeq Stranded Sample Prep Kit with human/mouse/rat Ribo Zero Gold
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2500 |
|
|
Description |
DES_rep3
|
Data processing |
FASTQ sequences were aligned to the mm9 genome using STAR v2.3.1z12 with default parameters Gene expression was quantified using HTSeq v0.6.1, using genic GTF from mm9 refGene Genome_build: mm9 Supplementary_files_format_and_content: Individual count tables generated as output from HTSeq
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|
|
Submission date |
Dec 05, 2018 |
Last update date |
Jul 17, 2019 |
Contact name |
Eiichi Okamura |
E-mail(s) |
eiokamu@gmail.com
|
Organization name |
Shiga University of Medical Science
|
Department |
Research Center for Animal Life Science
|
Lab |
Department of Stem Cells and Human Disease Models
|
Street address |
Seta, Tsukinowa-cho
|
City |
Otsu |
State/province |
Shiga |
ZIP/Postal code |
520-2192 |
Country |
Japan |
|
|
Platform ID |
GPL17021 |
Series (2) |
GSE123362 |
Esrrb function in the extraembryonic ectoderm is required for proper primordial germ cell specification [RNA-seq] |
GSE123363 |
Esrrb function is required for proper primordial germ cell development in presomite stage mouse embryos |
|
Relations |
BioSample |
SAMN10523694 |
SRA |
SRX5097638 |