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Sample GSM111130 Query DataSets for GSM111130
Status Public on Mar 01, 2008
Title Pancreas_E18.5_WT_rep1
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 764.8722
1415671_at 756.78754
1415672_at 1110.4966
1415673_at 161.9423
1415674_a_at 304.43643
1415675_at 404.0217
1415676_a_at 1230.0361
1415677_at 343.67404
1415678_at 665.403
1415679_at 1741.7388
1415680_at 446.80222
1415681_at 501.16776
1415682_at 336.80002
1415683_at 779.8842
1415684_at 180.32877
1415685_at 206.49548
1415686_at 393.9879
1415687_a_at 1012.99493
1415688_at 1064.9034
1415689_s_at 517.8594

Total number of rows: 45101

Table truncated, full table size 927 Kbytes.

Supplementary file Size Download File type/resource
GSM111130.CEL.gz 6.0 Mb (ftp)(http) CEL
GSM111130.CHP.gz 5.3 Mb (ftp)(http) CHP
Raw data provided as supplementary file
Processed data provided as supplementary file

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