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Sample GSM1246911 Query DataSets for GSM1246911
Status Public on Apr 02, 2014
Title IM015_RIPK3_Mock_d2_2
Sample type RNA
Source name IM015_RIPK3_Mock_d2
Organism Mus musculus
Characteristics tissue: Lung
mouse strain: RIPK3 knock-out
infection: Mock
Treatment protocol Lung tissue from each animal were harvested and briefly rinsed in cold (4ºC) PBS. Following the RNALater (Ambion) protocol, tissue was cut into small chunks (<0.5cm in any single dimension) and placed immediately into a 10-20 volumes (w/v) (e.g. 100mg/ml) RNALater. After a 4ºC incubation overnight, samples were stored at -80ºC until processing. Lung tissue was removed from RNALater, washed in a small volume of Trizol, homogenized in 10-20 volumes (w/v) Trizol and stored at -80°C until RNA isolation.
Extracted molecule total RNA
Extraction protocol All Trizol lysates were processed simultaneously: they were phase-separated, and RNA was isolated from the aqueous phase (diluted 2 fold with RLT buffer) using Qiagen RNeasy Mini columns and the manufacturer’s recommended protocol (Qiagen Inc., Valencia, CA). RNA quality was assessed on an Agilent 2100 Bioanalyzer using the nanochip format, and only intact RNA was used for microarray analyses.
Label Cy3
Label protocol The Agilent One-Color Microarray-Based Gene Expression Analysis Protocol was followed for the Cy3-cDNA probe preparation, followed by RNeasy column purification (QIAGEN, Valencia, CA). Dye incorporation and cRNA yield were checked with the NanoDrop ND-2000 Spectrophotometer.
Hybridization protocol The Agilent One-Color Microarray-Based Gene Expression Analysis Protocol was followed for hybridization and array washing. Two hundred fifty ng of each RNA sample was hybridized to one Agilent 4X44K mouse array.
Scan protocol Dry slides were scanned on an Agilent DNA microarray scanner (Model G2505B) using the XDR setting.
Data processing Raw images were analyzed using the Agilent Feature Extraction software (version and the GE1-v5_95_Feb07 extraction protocol. All arrays were required to pass Agilent QC flags. Extracted raw data were background corrected using the norm-exp method and quantile normalized using Agi4x44PreProcess and RMA Bioconductor packages.
Submission date Oct 22, 2013
Last update date Apr 02, 2014
Contact name Michael Katze
Organization name University of Washington
Department Microbiology
Lab Michael G. Katze, Ph.D
Street address Rosen Building 960 Republican St.
City Seattle
State/province WA
ZIP/Postal code 98109-4325
Country USA
Platform ID GPL7202
Series (1)
GSE51526 IM015 - Influenza infection of C57BL6 and RIPK3 knock-out mice

Data table header descriptions
VALUE Normalized log2 expression values for probes passing Agilent QC flags

Data table
A_51_P100021 7.114297604
A_51_P100034 12.73471124
A_51_P100063 8.800811016
A_51_P100084 7.475160558
A_51_P100099 10.76679053
A_51_P100155 11.48932481
A_51_P100174 10.91807254
A_51_P100181 9.219913683
A_51_P100227 10.56773522
A_51_P100246 10.96040988
A_51_P100289 11.76266034
A_51_P100298 9.675882062
A_51_P100327 8.634691466
A_51_P100347 5.956970581
A_51_P100379 7.230270733
A_51_P100428 6.491423491
A_51_P100470 5.876770871
A_51_P100505 10.64260329
A_51_P100537 7.333238222
A_51_P100565 11.83230597

Total number of rows: 31957

Table truncated, full table size 775 Kbytes.

Supplementary file Size Download File type/resource
GSM1246911_US93503719_251486838605_S01_GE1_107_Sep09_1_3.txt.gz 8.8 Mb (ftp)(http) TXT
Processed data included within Sample table

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