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Sample GSM2752175 Query DataSets for GSM2752175
Status Public on Aug 31, 2019
Title EGF_rep1
Sample type RNA
 
Source name Hela cells cultured with EGF for a week and transfected pT-Rex-DEST31 vector contained full-length PAX1 cDNA, which was not inducing to expression .
Organism Homo sapiens
Characteristics cell line: HeLa
Treatment protocol PAX1 (NM_006192) was constructed by inserting a full-length cDNA product into a pT-Rex-DEST31 vector. The construct was then transfected into HeLa cells with Lipofectamine 2000 in Opti-MEM I reduced-serum medium at 37 °C in a 5% CO2 atmosphere for 4–5 hours, after which the medium was removed and replaced with fresh culture medium. Cells were selected by the antibiotic (G418) after 2 days in culture. The stablelly transfected cells treated EGF (50ng/ml). The PAX1 expression was induced by using doxycycline.
Growth protocol Hela cells were cultured in Dulbecco's modified Eagle's medium (DMEM) or RPMI 1640 medium containing 10% (w/v) fetal calf serum, penicillin at 100 U/ml, streptomycin at 100 g/ml, and L-glutamine at 2 mmol/l.
Extracted molecule total RNA
Extraction protocol The total RNA was harvested by using a Qiagen RNeasy kit. An additional DNase I digestion procedure was included in the isolation of RNA to remove contaminating DNA according to the manufacturer's protocol. The mRNA quality has achieved the ratio of 28S/18S >1 and RNA quality indicator (RQI) > 7 by using Agilent 2100 620 Bioanalyzer to send to the core service unit (Health GeneTech Corp., Taoyuan, Taiwan) for whole genome expression analysis.
Label biotin
Label protocol Biotinylated cRNA were prepared with the Ambion MessageAmp kit for Illumina arrays.
 
Hybridization protocol Standard Illumina hybridization protocol
Scan protocol Standard Illumina scanning protocol
Description control
SAMPLE 1
Data processing The data were normalised using quantile normalisation with IlluminaGUI in R
 
Submission date Aug 23, 2017
Last update date Aug 31, 2019
Contact name Hung-Cheng Lai
E-mail(s) [email protected]
Organization name Taipei Medical University
Department Department of Obstetrics and Gynecology, School of Medicine, College of Medicine,
Street address No.250, Wuxing St.
City Taipei
ZIP/Postal code 11031
Country Taiwan
 
Platform ID GPL22366
Series (1)
GSE102986 PAX1-SET1B Interaction Drives Multiple Phosphatases and Inhibits Oncogenic Cascades

Data table header descriptions
ID_REF
VALUE quantile normalized
Detection Pval

Data table
ID_REF VALUE Detection Pval
6450255 111.2061 0.4116883
6370619 116.1906 0.2168831
2600039 100.9536 0.9
2650615 115.4277 0.2376623
5340672 105.3515 0.7246753
2000519 111.5777 0.387013
3870044 100.1469 0.9233766
7050209 109.4697 0.4961039
1580181 104.4952 0.7688312
5220554 103.5509 0.8038961
5390438 99.2149 0.9402598
6420681 106.1655 0.6844156
4760377 167.3418 0.001298701
2370438 108.1551 0.5688311
1740066 111.2737 0.4
4830092 120.3708 0.112987
3610072 313.1039 0
6480136 120.7299 0.1051948
4560202 107.9841 0.5792208
6180500 98.98872 0.9467533

Total number of rows: 34475

Table truncated, full table size 825 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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