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Sample GSM678898 Query DataSets for GSM678898
Status Public on Jan 24, 2012
Title Pdx1-Cre;KrasLSL-G12D vs. Pdx1-Cre;KrasLSL-G12D;IKK2/betaF/F pancreatic tissues
Sample type RNA
 
Channel 1
Source name cDNA from Pdx1-Cre;KrasLSL-G12D pancreas
Organism Mus musculus
Characteristics strain: C57BL/6 and 129
genotype: Pdx1-Cre;KrasLSL-G12D
tissue: pancreatic tumor
Biomaterial provider Jianhua Ling
Treatment protocol None.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from mouse pancreata using the Trizol method. The integrity and purity of RNA was determined by the Agilent BioAnalyzer.
Label Cy3
Label protocol Performed by following the protocol provided by Agilent.
 
Channel 2
Source name cDNA from Pdx1-Cre;KrasLSL-G12D;IKK2/betaF/F pancreas
Organism Mus musculus
Characteristics strain: C57BL/6 and 129
genotype: Pdx1-Cre;KrasLSL-G12D;IKK2/betaF/F
tissue: normal pancreas
Biomaterial provider Jianhua Ling
Treatment protocol None.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from mouse pancreata using the Trizol method. The integrity and purity of RNA was determined by the Agilent BioAnalyzer.
Label Cy5
Label protocol The Core Lab performed probe labeling using the protocol provided by Agilent.
 
 
Hybridization protocol The Core Lab performed the hybridization using the protocol provided by Agilent. Microarray experiments were carried out using whole human genome oligo arrays with 44k 60-mer probes (Agilent Technologies, Palo Alto, CA) with 500 ng of total RNA starting material.
Scan protocol The Core Lab performed image acquisition using the protocol provided by Agilent. The hybridized arrays were scanned with Agilent's dual laser-based scanner.
Data processing Feature Extraction software version 8.0 (Agilent Technologies) was used to link a feature to a design file and to determine the relative fluorescence intensity between the two samples. The VALUEs in the Sample data table represent Lowess-normalized log10 ratios (Cy5/Cy3). The VALUES in the 'GSE27478_fold_change_data.txt' file (which is linked to the Series GSE27478 record as a supplementary file) are the fold changes of KrasD/+,PDX1-CRE:KrasD/+, PDX1-CRE,IKK2F/ MICE. The detailed statistical analysis was performed as described by Price et al. Proc Natl Acad Sci USA. 2007 Feb 27;104(9):3414-9 (PMID 17360660).
 
Submission date Feb 23, 2011
Last update date Jan 24, 2012
Contact name Paul J Chiao
E-mail(s) [email protected]
Phone (713) 794-1030
Fax (713) 794-4830
Organization name The University of Texas M. D. Anderson Cancer Center
Department Department of Molecular and Cellular Oncology
Street address 1515 Holcombe Blvd
City Houston
State/province Texas
ZIP/Postal code 770300
Country USA
 
Platform ID GPL4134
Series (2)
GSE27478 Gene expression differences between the pancreatic tissues of Pdx1-Cre;KrasLSL-G12D and Pdx1-Cre;KrasLSL-G12D;IKK2/betaF/F mice
GSE33323 Kras-induced ikk2/nf-kappaB activation by IL-1 alpha and p62 freedforward loops is required for development of pancreatic ductal adenocarcinoma

Data table header descriptions
ID_REF
VALUE Lowess-normalized log10 ratio Cy5/Cy3)

Data table
ID_REF VALUE
12
13 0.174680667
14 0.206468867
15 0.176970132
16 -0.564250794
18 0.233955274
19
20 0.129565179
21 -0.06702594
22 0.161943758
23 0.254255678
24 -0.250330287
25 -0.537623262
26 0.293023899
27 0.201916183
28 -0.58934614
29 0.126827669
30 0.246973408
31
32 0.174560217

Total number of rows: 43379

Table truncated, full table size 711 Kbytes.




Supplementary file Size Download File type/resource
GSM678898.txt.gz 13.1 Mb (ftp)(http) TXT
Processed data included within Sample table
Processed data are available on Series record

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