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Sample GSM1139224 Query DataSets for GSM1139224
Status Public on Aug 04, 2013
Title EpiLCs, BP14A (clone #3-3), 36H, rep2
Sample type RNA
 
Source name EpiLCs induced from BVSCR26rtTA ESCs, harbouring Avi-Blimp1, 3xFLAG-Prdm14, V5-Tfap2c transgenes, differentiation time 36H
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, tetOx8-mCMV-3xFLAG-Prdm14-IRES-beta geo in piggyBac trasposon vector, tetOx8-mCMV-V5-Tfap2c-IRES-beta geo in piggyBac trasposon vector,
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.
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).
Extracted molecule total RNA
Extraction protocol total RNA was extracted using Qiagen RNeasy according to manufacturer's instruction
Label biotin
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)
 
Hybridization protocol Hybridization was performed according to the standard Affymetrix protocol (Affymetrix GeneChip Expression Analysis Technical Manual, 2004, Affymetrix: Eukaryotic Target Hybridization)
Scan protocol The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix)
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.
 
Submission date May 13, 2013
Last update date Jan 08, 2014
Contact name Fumio NAKAKI
E-mail(s) nakaki@anat2.med.kyoto-u.ac.jp
Phone +81-75-753-4343
Fax +81-75-751-7286
Organization name Kyoto University
Department Graduate School of Medicine
Lab Anatomy and Cell Biology
Street address Yoshidakonoe-cho, Sakyo-ku
City Kyoto
ZIP/Postal code 606-8501
Country Japan
 
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

Data table header descriptions
ID_REF
VALUE The Model-Based Expression Indices (MBEI) were calculated using the PM/MM difference mode with log-2 transformation of signal intensity.
ABS_CALL

Data table
ID_REF VALUE ABS_CALL
AFFX-BioB-5_at 8.72 P
AFFX-BioB-M_at 9.02 P
AFFX-BioB-3_at 8.81 P
AFFX-BioC-5_at 9.59 P
AFFX-BioC-3_at 10.31 P
AFFX-BioDn-5_at 11.56 P
AFFX-BioDn-3_at 11.86 P
AFFX-CreX-5_at 13.06 P
AFFX-CreX-3_at 13.14 P
AFFX-DapX-5_at 7.8 P
AFFX-DapX-M_at 9.25 P
AFFX-DapX-3_at 9.65 P
AFFX-LysX-5_at 5.24 P
AFFX-LysX-M_at 5.57 P
AFFX-LysX-3_at 7.28 P
AFFX-PheX-5_at 6 P
AFFX-PheX-M_at 6.58 P
AFFX-PheX-3_at 6.7 P
AFFX-ThrX-5_at 5.86 P
AFFX-ThrX-M_at 6.59 P

Total number of rows: 45101

Table truncated, full table size 806 Kbytes.




Supplementary file Size Download File type/resource
GSM1139224_12_EA1085_12_BP14A_3-3EpiLC_rep2.CEL.gz 5.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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