GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
Sample GSM686625 Query DataSets for GSM686625
Status Public on Mar 15, 2011
Title NIH3T3_DMSO_18hr_rep2
Sample type RNA
Source name NIH3T3, DMSO, 18hr, replicate 2
Organism Mus musculus
Characteristics cell line: NIH3T3
treatment: DMSO
Treatment protocol NIH3T3 cells were treated with DMSO, 50 nM rapamycin, or 2 mM PP242 for 18 hours
Growth protocol NIH3T3 cells were cultured in DMEM supplemented with 10% BCS and penicillin/streptomycin.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using QIAshredder and RNeasy Mini kits (Qiagen). RNA was quantified by Nanodrop and integrity was assessed on an Agilent 2100 Bioanalyzer.
Label Cy3
Label protocol RNA was amplified using the whole transcriptome amplification kits (Sigma) following the manufacturer’s protocol, and subsequent Cy3-CTP labeling was performed using one-color labeling kits (NimbleGen). The size distribution and quantity of the amplified product was assessed by Nanodrop and Bioanalyzer.
Hybridization protocol Equal amounts of Cy3 labeled target were hybridized to Agilent mouse whole genome 4x44K Ink-jet arrays. Hybridizations were performed for 14 hrs, according to the manufacturers protocol.
Scan protocol Arrays were scanned using the Agilent microarray scanner.
Description Gene expression in NIH3T3 cells after 18hr treatment with DMSO
Data processing Raw signal intensities were extracted with Feature Extraction v10.1 software. The dataset was normalized using the quantile normalization method. No background subtraction was performed, and the median feature pixel intensity was used as the raw signal before normalization.
Submission date Mar 07, 2011
Last update date Mar 15, 2011
Contact name Beatrice Wang
Organization name Univeristy of California, San Francisco
Street address 600 16th Street MC 2280
City San Francisco
State/province CA
ZIP/Postal code 94158
Country USA
Platform ID GPL7202
Series (1)
GSE27784 Transcriptional profiling of ATP-competitive mTOR inhibitors reveals mTORC1 and mTORC2 specific regulatory networks

Data table header descriptions
VALUE quantile normalized signal intensity

Data table
A_52_P616356 5.703903573
A_52_P580582 7.933290752
A_52_P403405 5.548179712
A_52_P819156 7.67271998
A_51_P331831 9.435323
A_51_P430630 6.648057926
A_52_P502357 5.373590215
A_52_P299964 7.641750724
A_51_P356389 6.001877287
A_52_P684402 9.529755888
A_51_P414208 6.319672121
A_51_P280918 10.47858004
A_52_P613688 5.548179712
A_52_P258194 6.687667284
A_52_P229271 8.682921453
A_52_P214630 10.94466453
A_52_P579519 9.632768055
A_52_P979997 5.548179712
A_52_P453864 5.548179712
A_52_P655842 7.113742166

Total number of rows: 41174

Table truncated, full table size 999 Kbytes.

Supplementary file Size Download File type/resource
GSM686625_251486829201_S01_GE1_105_Jan09_1_2.txt.gz 2.2 Mb (ftp)(http) TXT
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap