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Sample GSM1346504 Query DataSets for GSM1346504
Status Public on Mar 13, 2014
Title Clone#2_sham_rep1
Sample type RNA
Source name ERK1-GFP human keratinocytes_clone#2_sham
Organism Homo sapiens
Characteristics cell type: hTERT-immortalized normal human keratinocytes
tranfected with: ERK1-green fluorescent protein chimera
clone id: clone#2
treated with: none (untreated control)
Treatment protocol Treatments were performed in KSF supplemented with bovine pituitary extract (no epidermal growth factor). Conditions included 10ng/mL of TGFα used for ligand-activation; 10ug/mL of monoclonal antibody EGF antagonist mAB225 was used to shut down autocrine-activated ERK1; and nonspecific mouse IgG was used as a control for the autocrine-activated ERK1. Cells were harvested for RNA extraction after 24hrs. Three replicates were collected.
Growth protocol hTERT-immortalized normal human keratinocytes (provided by Dr. Jerry Shay, The University of Texas Southwestern Medical Center); Maintained in Keratinocyte serum-free medium (KSF) supplemented with bovine pituitary extract and epidermal growth factor. Stable RNA transfection of ERK1-green fluorescent protein chimera was achieved using Phoenix retroviral packing cell system and puromycin selection. Stable subclones were isolated with distinct ERK activation/oscillation patterns: Clone #1 exhibits transient ERK activation with ligand activation but does not oscillate; Clone #2 exhibits persistent ERK oscillations that are dependent on ligand activation; and Clong #3 exhibits spontaneous ERK oscillations in the absence of ligand activation.
Extracted molecule total RNA
Extraction protocol Total RNA was collected using the RNeasy Kit (Qiagen, Valencia, CA).
Label biotin
Label protocol Complementary DNA was synthesized from 1 µg of total RNA in the presence of an oligo-dT primer containing a T7 RNA polymerase promoter, and an in vitro transcription reaction was performed in the presence of a mixture of biotin-labeled ribonucleotides to produce biotinylated cRNA from the cDNA template, according to manufacturer’s protocols (Affymetrix One-Cycle Target Labeling Kit).
Hybridization protocol Biotin-labeled cRNA (12 µg) was fragmented to a size range between 50-200 bases for array hybridization. After hybridization, the arrays were washed and stained with streptavidin-phycoerythrin.
Scan protocol The arrays were scanned at a resolution of 2.5 microns using an Affymetrix GeneChip Scanner 3000.
Description TW11
Clone #2, sham
Data processing Raw intensity data were quantile normalized using Genespring software by Robust Multi-Array Analysis (RMA) summarization and probes were subject to quality control to measure the efficiency of transcription, integrity of hybridization, and consistency of qualitative calls.
Submission date Mar 12, 2014
Last update date Mar 13, 2014
Contact name Katrina M Waters
Organization name Pacific Northwest National Laboratory
Department Biological Sciences Division
Street address 902 Battelle Blvd; MSIN J4-18
City Richland
State/province WA
ZIP/Postal code 99352
Country USA
Platform ID GPL571
Series (1)
GSE55823 ERK Oscillation-Dependent Gene Expression Patterns and Deregulation By The Stress-Response

Data table header descriptions
VALUE Normalized Log2 signal intensity

Data table
AFFX-BioB-5_at 8.462362
AFFX-BioB-M_at 8.73297
AFFX-BioB-3_at 8.512617
AFFX-BioC-5_at 9.678446
AFFX-BioC-3_at 9.843988
AFFX-BioDn-5_at 10.767727
AFFX-BioDn-3_at 12.082661
AFFX-CreX-5_at 12.8775
AFFX-CreX-3_at 13.326855
AFFX-DapX-5_at 7.3242054
AFFX-DapX-M_at 8.911926
AFFX-DapX-3_at 9.786114
AFFX-LysX-5_at 5.176722
AFFX-LysX-M_at 5.179672
AFFX-LysX-3_at 6.23205
AFFX-PheX-5_at 5.6189885
AFFX-PheX-M_at 6.0699573
AFFX-PheX-3_at 7.344709
AFFX-ThrX-5_at 6.2420692
AFFX-ThrX-M_at 6.036596

Total number of rows: 22277

Table truncated, full table size 443 Kbytes.

Supplementary file Size Download File type/resource
GSM1346504_TW11.CEL.gz 2.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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