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Sample GSM902296 Query DataSets for GSM902296
Status Public on Mar 31, 2012
Title LT403Liver
Sample type RNA
Source name Doxycycline injected liver
Organism Mus musculus
Characteristics tissue: Liver
strain: C57BL/6J
genotype: TTD-
Treatment protocol mice (group: DEN induced liver tumors) were treated at day 15 with DEN (i.p.; 10µg/g bodyweight)
Growth protocol mice were kept in a pathogen-free environment
Extracted molecule total RNA
Extraction protocol RNA was isolated using the RNzol following the manufacturer's protocol. RNA was quantified using a NanoPhotometer and quality was monitored with the Agilent 2100 Bioanalyzer (Agilent Technologies).
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 0.5 ug RNA using the Quick Amp Labeling Kit (Agilent) according to the manufacturer's protocol, followed by RNAeasy column purification (QIAGEN, Valencia, CA). Dye incorporation and cRNA yield were checked with a NanoPhotometer
Hybridization protocol 1.65 µg of Cy3-labelled cRNA (specific activity >8.0 pmol Cy3/µg cRNA) was fragmented at 60°C for 30 minutes in a reaction volume of 55 µl containing 1x Agilent fragmentation buffer and 2x Agilent blocking agent following the manufacturer’s protocol. On completion of the fragmentation reaction, 55 µl of 2x Agilent HiRPM hybridization buffer was added to the fragmentation mixture and hybridized to Agilent Mouse GE 4x44K V2 Microarrays (G4846A) for 17 hours at 65°C in a rotating hybridization oven. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent), 1 minute with 37°C GE Wash buffer 2 (Agilent) and 30 seconds with Acetonitril.
Scan protocol Slides were scanned immediately after washing on the Agilent DNA microarray Scanner G2505B (5micron) with the the Agilent Scan Control Version A.8.4.1 .
Description Doxycycline
Data processing The scanned images were analyzed with Feature Extraction Software (Agilent). The data was preprocessed according to Agilent's Genespring software standard workflow. Gene expression levels were background corrected and signals for duplicated probes were summarized by geometric mean of non-compromised probes. After log2 transformation, a percentile shift normalization at the 75% level and a baseline shift to the median baseline of all probes was performed.
Submission date Mar 26, 2012
Last update date Apr 04, 2012
Contact name Hans A Kestler
Phone +49 731 5024248
Organization name University of Ulm
Department Research Group Bioinformatics and Systems Biology
Street address Albert-Einstein-Allee 11
City Ulm
ZIP/Postal code 89081
Country Germany
Platform ID GPL11202
Series (1)
GSE36813 Transient telomere dysfunction induces chromosomal instability and promotes carcinogenesis in telomerase-proficient mice

Data table header descriptions
VALUE Normalized intensity values (log2)

Data table
GE_BrightCorner 0.010391764
DarkCorner 0.019052633
A_55_P1989846 -1.120171174
A_55_P1991598 0.029240556
A_55_P2022211 -0.064991695
A_55_P1980764 0.944060409
A_55_P1964375 -0.058865631
A_51_P128876 0.060685324
A_55_P2121042 0.008003147
A_52_P219230 -0.114921606
A_51_P207591 0.872785481
A_55_P2131920 -0.002327976
A_55_P2404223 -0.059515609
A_55_P2101944 0.273124769
A_52_P358860 -0.639861751
A_51_P119031 0.482216483
A_51_P309854 0.285963917
A_51_P343900 -0.303922952
A_51_P234359 -0.03848338
A_51_P487813 -1.774297371

Total number of rows: 39485

Table truncated, full table size 1002 Kbytes.

Supplementary file Size Download File type/resource
GSM902296_US81503234_252665512417_S01_GE1_107_Sep09_1_3.txt.gz 8.9 Mb (ftp)(http) TXT
Processed data included within Sample table
Processed data provided as supplementary file

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