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Sample GSM2462185 Query DataSets for GSM2462185
Status Public on Jul 24, 2017
Title TOV-112D parental1
Sample type RNA
Source name Epithelial Ovarian Carcinoma cells no treated
Organism Homo sapiens
Characteristics tissue: ovarian cell line
histotype: endometrioid
Treatment protocol not applicable
Growth protocol not applicable
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from MCL cells using the TRIZOL Reagent (ThermoFisher) and validated for integrity and purity using the Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA).
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 0.1 ug RNA using the One-Color Low Input Quick Amp Labeling Kit (Agilent) according to the manufacturer's instructions, followed by RNAeasy column purification (QIAGEN, Valencia, CA). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
Hybridization protocol 1.6 ug of Cy3-labelled cRNA (specific activity >6.0 pmol Cy3/ug cRNA) was fragmented at 60°C for 30 minutes in a reaction volume of 55 ul containing 25x Agilent fragmentation buffer and 10x Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 55 ul of 2x Agilent Hi-RPMI hybridization buffer was added to the fragmentation mixture and hybridized to Agilent Whole Human Genome Oligo Microarrays (G4112A) for 17 hours at 65°C in a rotating Agilent hybridization oven. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent) and 1 minute with 37°C GE Wash buffer 2 (Agilent), then scan immediately.
Scan protocol Slides were scanned immediately after washing on the Agilent DNA Microarray Scanner (G2505B) using one color scan setting for 1x44k array slides (Scan Area 61x21.6 mm, Scan resolution 10um, Dye channel is set to Green and Dynamic Range of Green PMT is set to 100% and 10%).
Description Constitutive Gene expression of EOC cells.
Data processing The scanned images were analyzed with Feature Extraction Software (Agilent) using default parameters (protocol GE1-v107_Sep09 and Grid: 014850_D_F_20100430) to obtain background subtracted and spatially detrended Processed Signal intensities.
Submission date Jan 18, 2017
Last update date Jul 24, 2017
Contact name Riccardo Bomben
Phone +39 0434 659718
Organization name CRO Aviano
Department D-RT
Lab Clinical and Experimental Onco Hematology Unit
Street address Via Franco Gallini 2
City Aviano
ZIP/Postal code 33080
Country Italy
Platform ID GPL17077
Series (2)
GSE93793 Characterization of three Epithelial Ovarian Cancer cell lines resistant to cisplatin (mRNA).
GSE93795 Characterization of three Epithelial Ovarian Cancer cell lines resistant to cisplatin.

Data table header descriptions
VALUE Normalized signal intensity

Data table
GE_BrightCorner 0.012580872
DarkCorner -0.09996581
A_23_P117082 1.8719568
A_33_P3246448 -0.49352312
A_33_P3318220 -0.47828555
A_33_P3236322 0.6322112
A_33_P3319925 0.07937479
A_21_P0000509 0.6182289
A_21_P0000744 -0.98309517
A_24_P215804 -0.5407591
A_23_P110167 -8.006924
A_33_P3211513 -0.121198654
A_23_P103349 -0.025265455
A_32_P61480 -1.1306946
A_33_P3788124 0.7768202
A_33_P3414202 -1.4029217
A_33_P3316686 -0.7019086
A_33_P3300975 -1.4278297
A_33_P3263061 -0.30563164
A_33_P3261373 -0.47538114

Total number of rows: 50739

Table truncated, full table size 1228 Kbytes.

Supplementary file Size Download File type/resource
GSM2462185_US45102827_253949416319_S01_GE1_1105_Oct12_2_1_TOV112d_1.txt.gz 12.5 Mb (ftp)(http) TXT
Processed data included within Sample table

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