|
Status |
Public on Jul 15, 2019 |
Title |
WT replicate 2 |
Sample type |
RNA |
|
|
Source name |
WT_extraembryonic ectoderm
|
Organism |
Mus musculus |
Characteristics |
strain background: C57BL/6J developmental stage: E6.5 embryo genotype/variation: wild type tissue: Extraembryonic ectoderm
|
Treatment protocol |
Post-implantation embryos were dissected from the uteri of pregnant females at E6.5. Extraembryonic ectoderm was separated and pooled (~20-25 per replicate)
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using Trizol, and the quality of the RNA was assessed using a BioAnalyzer
|
Label |
Biotin
|
Label protocol |
100 ng of RNA from each pooled sample was used to generate cDNA, which was then fragmented and labeled using the Ambion WT Expression Kit according to the manufacturer's protocol
|
|
|
Hybridization protocol |
cDNA was then hybridized to Mouse 1.0 ST gene array v1 according to the manufacturer’s protocol
|
Scan protocol |
Chip was scanned with an Affymetrix GeneChip Scanner 7G
|
Description |
WT_rep2
|
Data processing |
The raw data was imported and normalized using the affy R package v.1.44.0
|
|
|
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 |
GPL6246 |
Series (2) |
GSE123360 |
Esrrb function in the extraembryonic ectoderm is required for proper primordial germ cell specification [microarray] |
GSE123363 |
Esrrb function is required for proper primordial germ cell development in presomite stage mouse embryos |
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