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Sample GSM1339262 Query DataSets for GSM1339262
Status Public on Apr 01, 2015
Title hypoxia serum plus
Sample type RNA
 
Source name hypoxia serum plus
Organism Homo sapiens
Characteristics cell line: OVSAYO
cell type: human ovarian cancer cells
culture condition: hypoxia serum plus
culture duration: 16 hours
Growth protocol An ovarian cancer cell line, OVSAYO was cultured under four culture conditions (normoxia and fetal calf serum (FCS) plus, normoxia and FCS minus, hypoxia and FCS plus, and hypoxia and FCS minus conditions) in RPMI1640 medium for 16 hours.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using SV total RNA isolation kit (Promega, Madison, WI, USA) according to recommended standard protocol.
Label Cy3
Label protocol Labeling (Cy3) was performed using NimbleGen one-colour DNA labeling kit (Roche, Indianapolis, IN, USA) according to recommended standard operating protocol provided with gene expression microarray.
 
Hybridization protocol Hybridization to 2006-08-03_HG18_60mer_expr array (Euk expr 385K catalog Arr Del (NimbleGen, Roche, Madison, WI, USA)) was performed using NimbleGen Hybridization kit (Roche, Madison, WI, USA) according to recommended standard operating protocol provided with gene expression microarray.
Scan protocol Scanning was performed by NimbleScan v2.6 software using GenePix Personal 4100A instrument (Axon Instruments, Sunyvale, CA, USA).
Description OVSAYO cells were cultured under 1%O2 with 10%FCS for 16h.
Data processing Scanned TIFF images were processed by NimbleScan v2.6 software (Roche NimbleGen, Inc.) to obtain raw data (pair) files. Data were further processed by same software to obtain normalized data (norm_RMA.pair and RMA.Calls files). These data were analyzed by contract research service at Subio Inc. (Kagoshima, Japan, www.subio.jp/) using Subio platform v 1.14 software.
 
Submission date Mar 04, 2014
Last update date Apr 01, 2015
Contact name Shiro Koizume
E-mail(s) skoizume@gancen.asahi.yokohama.jp
Organization name Kanagawa Cancer Center Research Institute
Street address 2-3-2 Nakao Asahi-ku
City Yokohama
State/province Please Select
ZIP/Postal code 241-8515
Country Japan
 
Platform ID GPL15143
Series (2)
GSE55564 Identification of genes activated in cancer cells cultured under hypoxia and serum-free condition
GSE55565 Identification of genes activated under CoCl2 treatment in an Sp1 dependent manner and under hypoxia without serum condition in an ovarian cancer cell line

Data table header descriptions
ID_REF
VALUE RMA normalized signal intensity

Data table
ID_REF VALUE
AB000409 390.0586
AB000461 2870.5811
AB000463 897.7770
AB000781 59.3807
AB001025 507.9567
AB001328 48.1060
AB002294 1128.5734
AB002308 4712.8109
AB002311 508.0144
AB002313 10771.5203
AB002360 534.9249
AB002372 55.0888
AB002377 356.9204
AB002381 1286.0207
AB002382 17545.6474
AB002384 42.9992
AB003177 940.2728
AB003333 2384.9445
AB004885 629.2618
AB006589 203.1685

Total number of rows: 47633

Table truncated, full table size 874 Kbytes.




Supplementary file Size Download File type/resource
GSM1339262_415651_532.pair.gz 7.5 Mb (ftp)(http) PAIR
GSM1339262_415651_532_RMA.calls.gz 3.3 Mb (ftp)(http) CALLS
Processed data included within Sample table
Processed data provided as supplementary file

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