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Sample GSM111131 Query DataSets for GSM111131
Status Public on Mar 01, 2008
Title Pancreas_E18.5_WT_rep2
Sample type RNA
Source name pooled pancreata, embryonic day 18.5, wild type
Organism Mus musculus
Characteristics Strain: B6D2
Developmental stage: embryonic day 18.5
Tissue: pooled pancreata
Genotype: wild type
Treatment protocol HNF6 expression was driven specifically to pancreatic endocrine cells beginning at embryonic day (e) 11.5 using a 1 kb enhancer from the 5’ pdx1 promoter region. This transgenic line, termed pdx1PBHnf6, was maintained on an inbred hybrid (B6D2) background. All mice were kept on a 12 hour light/dark cycle, fed Mouse diet 5015 (LabDiet), and given water ad lib. For embryonic analyses, the morning of the vaginal plug was considered e0.5. All mouse studies were performed in accordance with the Vanderbilt Institutional Animal Care and Use Committee guidelines under the supervision of the Division of Animal Care.
Extracted molecule total RNA
Extraction protocol Pancreata were dissected at e18.5 and postnatal day 1 in ice cold PBS and immediately placed into RNAlater (Ambion). Total pancreatic RNA was isolated using RNAqueous RNA Isolation Kit (Ambion) according to the manufacturer’s instructions. Agilent’s Bioanalyzer microfluidic assay (Agilent Technologies, Palo Alto CA) was used to assay RNA integrity. Spectrophotometric and fluorometric methods were combined to quantitate protein and nucleic acids present in the sample, and to ensure quality control of each sample. RNA samples were bioanalyzed individually and highly pure samples were pooled according to their genotype (3-5 animals per pool) in order to obtain an adequate quantity of RNA.
Label biotin
Label protocol Following quality control, the RNA was prepared for microarray analysis using the standard Affymetrix protocol (Affymetrix Inc, Santa Clara, CA). Briefly, a total of 5 µg of total RNA was reverse transcribed to double-stranded (ds) cDNA using an oligo-dT primer coupled to a T7 promoter. In vitro transcription from the ds cDNA was then carried out using T7 polymerase and incorporating biotin-modified CTP and UTP ribonucleotides.
Hybridization protocol The biotinylated cRNA (15 µg) was fragmented and hybridized to an Affymetrix GeneChip Mouse Genome 430 2.0 Array containing 45,000 sets of 11 to 25-mer oligomers, representing 39,000 mouse transcripts (34,000 are annotated as well-defined genes). Hybridized cRNA was detected using streptavidin coupled to phycoerythrin.
Scan protocol GeneChips were scanned using GeneChip Scanner 3000 7G Plus 2 and GeneChip Operating System (GCOS, Affymetrix, Santa Clara, CA). Default values were used to grid images (.DAT) and generate .CEL and .CHP files.
Description No additional description necessary
Data processing CEL files (raw Affymetrix data) were imported in GeneSpring 7.0 (Agilent Technologies) and transformed by RMA (Robust Multichip Analysis). The
Submission date May 25, 2006
Last update date Aug 28, 2018
Contact name Laura Crawford
Organization name Vanderbilt University
Department Diabetes, Endocrinology, & Metab Division
Lab Gannon Lab
Street address 715 PRB 2220 Pierce Ave
City Nashville
State/province TN
ZIP/Postal code 37232
Country USA
Platform ID GPL1261
Series (1)
GSE4926 Gene expression profiling of a mouse model of islet dysmorphogenesis
Reanalyzed by GSE119085

Data table header descriptions
VALUE RMA-transformed signal intensity value

Data table
1415670_at 809.1678
1415671_at 756.36633
1415672_at 1309.6134
1415673_at 170.4861
1415674_a_at 302.5052
1415675_at 414.71347
1415676_a_at 1264.4847
1415677_at 368.43793
1415678_at 736.4117
1415679_at 1740.431
1415680_at 425.5045
1415681_at 517.15625
1415682_at 337.71143
1415683_at 778.13336
1415684_at 176.26689
1415685_at 217.30002
1415686_at 393.84778
1415687_a_at 1042.68
1415688_at 1121.9667
1415689_s_at 539.44403

Total number of rows: 45101

Table truncated, full table size 927 Kbytes.

Supplementary file Size Download File type/resource
GSM111131.CEL.gz 6.1 Mb (ftp)(http) CEL
GSM111131.CHP.gz 5.2 Mb (ftp)(http) CHP
Raw data provided as supplementary file
Processed data provided as supplementary file

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