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Sample GSM738125 Query DataSets for GSM738125
Status Public on May 22, 2012
Title Zic3 NPCc2
Sample type RNA
Source name ZiNPC
Organism Homo sapiens
Characteristics cell type: ZiNPC derived from BJ1 fibroblasts
gender: male
cell line: BJ1
treatment: Zic3, KLF4, OCT4 and SOX2
Biomaterial provider SCIL
Treatment protocol The coding region of the mouse Zic3 gene was amplified by RT-PCR and cloned in pMIG-IRES-GFP plasmid (Addgene). The pMXs plasmids encoding for OCT4, SOX2 and KLF4 were purchased from Addgene. pMXs and pMIG-based retroviral vectors were transfected individually along with the viral packaging genes gag-pol (Addgene) and VSVG (Addgene) into 293T cells (ATCC) using Fugene HD reagent (Roche) according to the manufacturer's directions. Human BJ1 cells (Lonza) were seeded at 1.5 x 105 cells/well in 6-well plates (Sigma) without feeders. Cells were transduced with Zic3, KLF4, OCT4 and SOX2 retroviral vector containing supernatants mixed equally. To achieve maximum transduction efficiency, cells were transduced twice with the viral supernatant. Four days after transduction, the transduced cells were reseeded at 1.5 x 105 cells per 100-mm dish containing MEF and cultured with hESC medium. ZiNPC were picked in 15-20 days post transduction.
Growth protocol mTESR medium
Extracted molecule total RNA
Extraction protocol Rneasy (Qiagen)
Label biotin
Label protocol RNA concentration and purity were determined spectrophotometrically using the Nanodrop ND-1000 (Nanodrop Technologies) and RNA integrity was assessed using a Bioanalyser 2100 (Agilent). Using the Ambion WT Expression Kit, per sample, an amount of 100 ng of total RNA spiked with bacterial poly-A RNA positive controls (Affymetrix) was converted to double stranded cDNA in a reverse transcription reaction. Next the sample was converted and amplified to antisense cRNA in an in vitro transcription reaction which was subsequently converted to single stranded sense cDNA. Finally, samples were fragmented and labeled with biotin in a terminal labeling reaction according to the Affymetrix WT Terminal Labeling Kit.
Hybridization protocol A mixture of fragmented biotinylated cDNA and hybridisation controls (Affymetrix) was hybridised on Affymetrix  GeneChip Human Gene 1.1 ST Array Plate followed by staining and washing in the GeneTitan® Instrument (Affymetrix) according to the manufacturer's procedures.
Scan protocol To assess the raw probe signal intensities, chips were scanned using the GeneTitan® HT Array Plate Scanner (Affymetrix).
Description BJ1 fibroblast transduced with OCT4, SOX2, KLF4 and Zic3
Data processing RMA-normalized expression values as obtained with the xps package (version 1.10.2) of BioConductor
Submission date Jun 07, 2011
Last update date May 23, 2012
Contact name Rekin's Janky
Organization name VIB
Department Nucleomics Core
Street address Herestraat 49 Box 816
City Leuven
ZIP/Postal code B-3000
Country Belgium
Platform ID GPL11532
Series (1)
GSE29770 Transduction of human fibroblasts with Zic3 combined with OCT4, SOX2 and KLF4 induces stable neural progenitor cell lines

Data table header descriptions
VALUE RMA-normalized expression values as obtained with the xps package (version 1.10.2) of BioConductor

Data table
7896736 6.397399115
7896738 3.345424763
7896740 3.496743549
7896742 10.75187875
7896744 6.64135383
7896746 9.066923344
7896748 6.305607613
7896750 3.379842727
7896752 11.01643225
7896754 9.142719753
7896756 4.228726355
7896759 7.362066551
7896761 5.90411314
7896779 7.683773639
7896798 6.280516537
7896817 5.727607383
7896822 7.47634118
7896859 4.385748533
7896861 3.728421228
7896863 4.651241167

Total number of rows: 28204

Table truncated, full table size 547 Kbytes.

Supplementary file Size Download File type/resource
GSM738125_hyb10334.CEL.gz 4.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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