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Status |
Public on Aug 04, 2013 |
Title |
B (clone #2-4) +Doxycycline, day1, rep2 |
Sample type |
RNA |
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Source name |
Aggregates of EpiLCs on day1, induced from BVSCR26rtTA ESCs, harbouring Avi-Blimp1 transgenes, cultured with doxycycline
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Organism |
Mus musculus |
Characteristics |
gender: Male strain: C57BL/6;129 transgene: Blimp1-mVenus, stella-ECFP, Rosa26-rtTA, tetOx8-mCMV-Avi-Blimp1-IRES-beta geo-bGH pA in piggyBac trasposon vector
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Treatment protocol |
After 36 hrs of differentiation, cells were harvested and cultured in a Lipidure-Coat 96-well plate (NOF) to be aggregated (started with 2,000 cells/well) in GK15 with 1.5 μg/ml of Dox (Clonetech). After 24 hrs aggregation culture, whole cells from the aggregates were harvested.
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Growth protocol |
Transfected ESCs were maintained under 2i+LIF condition and adapted to a feeder-free condition prior to induction. EpiLC differentiation was performed as reported previously (Hayashi et al., Cell, 2011).
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Extracted molecule |
total RNA |
Extraction protocol |
total RNA was extracted using Qiagen RNeasy according to manufacturer's instruction
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Label |
biotin
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Label protocol |
Biotinylated cRNA were prepared from total RNA according to the standard Affymetrix protocol (Affymetrix GeneChip Expression Analysis Technical Manual, 2004, Affymetrix: Eukaryotic One-Cycle Target Labeling Assay)
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Hybridization protocol |
Hybridization was performed according to the standard Affymetrix protocol (Affymetrix GeneChip Expression Analysis Technical Manual, 2004, Affymetrix: Eukaryotic Target Hybridization)
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Scan protocol |
The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix)
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Data processing |
CEL data were generated by GeneChip Operating Software and then subjected to the dCHIP software. Data were normalized together with the default settings.
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Submission date |
May 13, 2013 |
Last update date |
Aug 04, 2013 |
Contact name |
Fumio NAKAKI |
E-mail(s) |
[email protected]
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Phone |
+81-75-753-4343
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Fax |
+81-75-751-7286
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Organization name |
Kyoto University
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Department |
Graduate School of Medicine
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Lab |
Anatomy and Cell Biology
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Street address |
Yoshidakonoe-cho, Sakyo-ku
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City |
Kyoto |
ZIP/Postal code |
606-8501 |
Country |
Japan |
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Platform ID |
GPL1261 |
Series (2) |
GSE46854 |
Induction of the mouse germ cell fate by transcription factors in vitro [exp2] |
GSE46855 |
Induction of the mouse germ cell fate by transcription factors in vitro |
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