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Sample GSM2932739 Query DataSets for GSM2932739
Status Public on Dec 01, 2018
Title iPSC-NCCs 2
Sample type RNA
 
Source name iPSC-NCCs
Organism Homo sapiens
Characteristics cell type: iPSCs-derived neural crest cells (NCCs)
time point: at the end of the induction
Growth protocol The iPSCs were cultured under the feeder-free and serum-free condition with AK03N medium (Ajinomoto) on the 6-well culture plate coated with iMatrix-511 (Nippi). After the undifferentiated iPSCs reached confluence in culture, the iPSCs were dissociated with Accutase (Millipore) and seeded first on the 3-D culture plate (EZSPHERE®, AGC TECHNO GLASS) at a density of 2×10^5 cells/mL in embryoid body (EB) induction medium which composed from DMEM/F12 (Sigma-Aldrich) supplemented with 1% N-2 (GIBCO), 2% MACS® NeuroBrew-21 (Miltenyi Biotec), 2 mM L-glutamine (Sigma-Aldrich), 20 ng/ml recombinant human epidermal growth factor (EGF: PeproTech), 1% penicillin/streptomycin (GIBCO) and 10 μM Y-27632 (Wako). The spent medium was changed once on EB culture day 4 and uniformly sized EBs were formed in 7 days. Subsequently, the EBs were replated on non-coated 10 cm dish in NCCs induction medium, DMEM/F12 with 1% N-2, 2 mM L-glutamine, 1% penicillin/streptomycin, 20 ng/ml EGF, 20 ng/ml recombinant human fibroblast growth factor-basic (bFGF: Wako), and 5 μg/ml heparin (Sigma-Aldrich). To allow the EBs to attach the culture dish and induced NCCs to migrate from the attached EBs, the culture dish was stand for first 3 days and the spent medium was changed on days 4, 8, 11, 13, and 14 after re-plating of the EBs. NCCs induction was completed on day 14. .
Extracted molecule total RNA
Extraction protocol The total RNA of iPSCs (n=2) and iPSC-NCCs (n=2) were extracted by High Pure RNA Isolation Kit (Roche) after the cells were harvested.
Label biotin
Label protocol We followed protocol of manual that is GeneChip® WT PLUS Reagent Kit User Manual.
 
Hybridization protocol We followed protocol of manual that is GeneChip® WT PLUS Reagent Kit User Manual.
Scan protocol We followed manufacturer's protocol, and used GeneChip® Scanner 3000 7G.
Description neural crest 2
Data processing Data acquisition and normalization (SST-RMA) were used Affymetrix® Expression Console™ Software.
 
Submission date Jan 12, 2018
Last update date Dec 02, 2018
Contact name Shota Fujii
Organization name RIKEN Center for Developmental Biology
Department The Laboratory for Retinal Regeneration
Street address 2-2-3 Minatojima-minamimachi, Chuo-ku
City Kobe
ZIP/Postal code 650-0047
Country Japan
 
Platform ID GPL23159
Series (1)
GSE109136 Immunological properties of neural crest cells derived from human induced pluripotent stem cells (resting state)

Data table header descriptions
ID_REF
VALUE normalized

Data table
ID_REF VALUE
TC0100006437.hg.1 51.98954
TC0100006476.hg.1 60.78405
TC0100006479.hg.1 175.1735
TC0100006480.hg.1 47.50935
TC0100006483.hg.1 43.13408
TC0100006486.hg.1 239.2436
TC0100006490.hg.1 52.4281
TC0100006492.hg.1 115.0193
TC0100006494.hg.1 43.47528
TC0100006497.hg.1 36.99446
TC0100006499.hg.1 199.005
TC0100006501.hg.1 82.00361
TC0100006502.hg.1 31.27381
TC0100006514.hg.1 23.49146
TC0100006516.hg.1 55.02615
TC0100006517.hg.1 35.72331
TC0100006524.hg.1 53.01942
TC0100006540.hg.1 130.4741
TC0100006548.hg.1 23.24824
TC0100006550.hg.1 490.885

Total number of rows: 24351

Table truncated, full table size 659 Kbytes.




Supplementary file Size Download File type/resource
GSM2932739_neural_crest-RNA_2_Clariom_S_Human_.CEL.gz 1.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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