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Sample GSM934066 Query DataSets for GSM934066
Status Public on Mar 22, 2013
Title Dox-treated lung Replicate 1
Sample type RNA
 
Source name Diseased
Organism Mus musculus
Characteristics tissue: Lung
strain: BALB/c
transgene: IL-1b
treatment: doxycyline
Growth protocol Lungs were harvested from water- or Dox-treated mice after 7 days at ~12-week of age. IL-1b is induced in Dox-treated mice which showed increased inflammation and emphysema in lung.
Extracted molecule total RNA
Extraction protocol Reaction purification is achieved using magnetic binding beads for cDNA and Qiagen RNeasy kits for cRNA purification.
Label Biotin
Label protocol The final in vitro transcription incorporates biotin moieties that are later labeled with phycoerythrin. After amplification, samples are put through a controlled fragmentation to improve hybridization sensitivity and consistency. The labeled molecules are biotinylated-cRNA.
 
Hybridization protocol GeneChip microarrays are loaded with the fragmented target sample/hybridization buffer mix using standard manual techniques. Arrays are hybridized for 18 hours at 45?C with vigorous mixing. Unbound sample is removed and staining is accomplished through the binding of streptavidin conjugated phycoerythrin to the hybridized target. Excess label is removed. Washing and staining steps are performed by the Affymetrix FS450 fluidics station using standard protocols.
Scan protocol Arrays are scanned using a GeneChip Scanner 3000 7G with a 48 array autoloader. The scanner maintains the optimal temperature for the arrays prior to and during scanning.
Description Dox-treated lung replicate 1
Data processing Data were loaded into the Rosetta Resolver system (Rosetta Biosoftware, Seattle, WA) and processed using the RMA algorithm (http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=PubMed&list_uids=12582260). Intensities were calculated based on RMA, a Rosetta-developed error, and a MAS-5 p-value. The Rosetta-developed error is used in the calculation of xdev for the ratio p-values as described in section 2.2 (http://bioinformatics.oxfordjournals.org/cgi/content/full/22/9/1111).
 
Submission date May 21, 2012
Last update date Mar 22, 2013
Contact name I-Ming Wang
E-mail(s) i_ming_wang@merck.com
Phone 215-652-1287
Organization name Merck Research Lab
Department Genetics and Pharmacogenomics
Lab Discovery Pharmacogenomics
Street address 770 Sumneytown Pike
City West Point
State/province PA
ZIP/Postal code 19486
Country USA
 
Platform ID GPL6794
Series (2)
GSE31559 Various mice and rat tissues subjected to various treatments
GSE38075 Profiling whole lung from lung-specific IL-1b-Tg mice

Data table header descriptions
ID_REF
VALUE RMA normalized intensity

Data table
ID_REF VALUE
merck-NM_009141_at 765.85
merck-NM_001033800_at 19.76
merck-NM_001037912_at 58.85
merck-NM_001034889_at 12.15
merck-NM_001033802_at 13.14
merck-NM_001037919_s_at 5.36
merck-NM_001039226_at 7.06
merck-NM_001018010_at 7.91
merck-NM_001037920_at 10.27
merck-NM_029460_x_at 9.56
merck-NM_001039230_at 7.32
merck-NM_001025240_s_at 7.78
merck-NM_001013379_s_at 48.87
merck-NM_001039206_at 60.84
merck-NM_173782_at 36.59
merck-NM_001024729_at 21.03
merck-NM_001033495_s_at 6.42
merck-NM_001024710_at 20.25
merck-NM_001039235_at 12.5
merck-NM_001015506_at 11.86

Total number of rows: 43681

Table truncated, full table size 1122 Kbytes.




Supplementary file Size Download File type/resource
GSM934066__52048700761067091208403547596393.CEL.gz 3.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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