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Sample GSM349887 Query DataSets for GSM349887
Status Public on Dec 01, 2009
Title 251485028601_4
Sample type RNA
 
Source name ovarian cancer cell line
Organism Homo sapiens
Characteristics ANXA11_RNAi
24 hours
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using TRIZOL reagent (Invitrogen) followed by RNeasy mini kit with DNase on-column digestion (Qiagen). RNA was quantified with NanoDrop ND-1000 followed by quality assessment with the 2100 Bioanalyzer (Agilent) according to manufacturer’s protocol
Label Cy3
Label protocol Total RNA was labeled using Agilent Low RNA Input Fluorescent Linear Amplification Kit (Agilent) following the manufacturer’s instruction with minor modifications. Briefly, 0.4 µg RNA was reverse-transcribed into cDNA by MMLV-RT using an oligo dT primer (System Biosciences) that incorporated a T7 promoter sequence. The cDNA was then used as a template for in vitro transcription in the presence of T7 RNA polymerase and Cyanine-3 labeled CTPs (Perkin Elmer). RNA spike-in controls (Agilent) were added to RNA samples before amplification and labeling. The labeled cRNA was purified using RNeasy mini kit (Qiagen).
 
Hybridization protocol Total 0.825 µg of each Cy3-labeled sample was used for hybridization on Agilent 4x 44K whole human genome microarray at 65ºC for 17 hours in a hybridization oven with rotation.
Scan protocol Slides were scanned using the Agilent Microarray Scanner controlled by Agilent Scan Control 7.0 software.
Description R4
Data processing Microarray data were extracted with Agilent Feature Extraction 9.5.3.1 software and imported into GeneSpring GX 9.0.1 (Agilent). Normalization was done with all intensities higher than 5, log2 transformation and cross-array quartile normalization. Features with intensities smaller than 300 at all time points were excluded from the analysis.
 
Submission date Dec 10, 2008
Last update date Dec 10, 2008
Contact name Jin Song
E-mail(s) jsong20@jhmi.edu
Phone 4105020419
Fax 410-502-7882
Organization name Johns Hopkins Medical Institutions
Department Pathology
Lab Center for Biomarker Discovery
Street address 419 N. Caroline Str.
City Baltimore
State/province MD
ZIP/Postal code 21231
Country USA
 
Platform ID GPL6480
Series (1)
GSE13893 Dynamic response of annexin A11-associated gene expression to cisplatin treatment

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
A_23_P100001 48.81071568
A_23_P100011 58.06045609
A_23_P100022 90.71298668
A_23_P100056 8.055758868
A_23_P100074 1418.611665
A_23_P100092 514.9933525
A_23_P100103 52.40405333
A_23_P100111 142.1891528
A_23_P100127 462.8243632
A_23_P100133 62.39631829
A_23_P100141 146.66634
A_23_P100156 177.1402193
A_23_P100177 36.33510071
A_23_P100189 101.637008
A_23_P100196 2167.33132
A_23_P100203 4427.924783
A_23_P100220 7119.775324
A_23_P100240 272.150146
A_23_P10025 13.39739218
A_23_P100263 770.0114028

Total number of rows: 41000

Table truncated, full table size 983 Kbytes.




Supplementary file Size Download File type/resource
GSM349887.txt.gz 7.8 Mb (ftp)(http) TXT
Processed data included within Sample table

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