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Sample GSM1842579 Query DataSets for GSM1842579
Status Public on Sep 29, 2015
Title SCC-FAK-wt_rep1
Sample type RNA
Source name SCC FAK-wt cells
Organism Mus musculus
Characteristics background strain: FVB
genotype: K14CreER FAKflox/flox
cell type: Squamous cell carcinoma
Treatment protocol Cells were washed three times with ice-cold phosphate-buffered saline.
Growth protocol Cells were cultured in Glasgow minimum essential medium (MEM) (Sigma) supplemented with 2 mM L-glutamine, MEM vitamins, 1 mM sodium pyruvate (all Sigma), MEM amino acids, and 10% fetal bovine serum (both Life Technologies). Cell lines re-expressing FAK-wt were maintained under selection using 0.25 mg/ml hygromycin.
Extracted molecule total RNA
Extraction protocol Total RNA extraction and on-column DNase I digestion were performed using an RNeasy kit (Qiagen) according to manufacturer's instructions.
Label biotin
Label protocol cDNA synthesis and amplification was performed using the Ovation Pico WTA System V2 (NuGEN Technologies) with an input of 50 ng total RNA according to manufacturer’s instructions. PolyA controls (Affymetrix, part no. 900433) were included at the same concentration as the sample. 5 µg of the cDNA was then fragmented and biotin labelled using an Encore Biotin Module kit (NuGEN) according to manufacturer’s instructions.
Hybridization protocol Fragmented and labelled cDNA was hybridised to GeneChip Mouse Genome 430 2.0 Arrays (Affymetrix) for 16 h at 45 ºC with rotation at 60 rpm. Arrays were washed and stained using the Affymetrix GeneChip Fluidics Station 450 using protocol EukGE-WS2v4_450.
Scan protocol Arrays were scanned using the Affymetrix GeneChip Scanner 3000 system with autoloader and AGCC software.
Description Gene expression data from SCC FAK-wt cells
Data processing Gene expression data were analyzed using packages within Bioconductor implemented in the R statistical programming language. The gene expression data were summarised from CEL files using Ensembl gene identifiers (BRAINARRAY v17.0.0), ENSG and normalized using the Robust Multi-array Average (RMA) algorithm within the ‘affy’ package.
Submission date Aug 03, 2015
Last update date Sep 29, 2015
Contact name Adam Byron
Organization name University of Edinburgh
Department Edinburgh Cancer Research UK Centre
Street address Western General Hospital, Crewe Road South
City Edinburgh
ZIP/Postal code EH4 2XR
Country United Kingdom
Platform ID GPL20766
Series (1)
GSE71662 Gene expression data from mouse squamous cell carcinoma cells

Data table header descriptions
VALUE log2 RMA signal

Data table
ENSMUSG00000000001_at 10.88813431
ENSMUSG00000000003_at 2.077340317
ENSMUSG00000000028_at 8.503491292
ENSMUSG00000000031_at 3.196346639
ENSMUSG00000000037_at 3.899000022
ENSMUSG00000000049_at 3.617585134
ENSMUSG00000000056_at 7.566620051
ENSMUSG00000000058_at 9.421845773
ENSMUSG00000000078_at 10.27189519
ENSMUSG00000000085_at 5.015090758
ENSMUSG00000000088_at 12.00122141
ENSMUSG00000000093_at 3.778965806
ENSMUSG00000000094_at 4.006494486
ENSMUSG00000000103_at 6.333759984
ENSMUSG00000000120_at 4.82104209
ENSMUSG00000000125_at 2.838560467
ENSMUSG00000000126_at 4.873951282
ENSMUSG00000000127_at 8.645222907
ENSMUSG00000000131_at 8.73487236
ENSMUSG00000000134_at 8.459292296

Total number of rows: 17204

Table truncated, full table size 569 Kbytes.

Supplementary file Size Download File type/resource
GSM1842579_Frame_Musmu_SCC-FAK-wt1.CEL.gz 3.6 Mb (ftp)(http) CEL
Raw data provided as supplementary file
Processed data included within Sample table

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