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Sample GSM1149525 Query DataSets for GSM1149525
Status Public on May 28, 2013
Title SJL-ChrY^B10.S, young, CD4 T cell, rep1
Sample type RNA
 
Source name SJL-ChrY^B10.S, CD4+TCRB+ cells, naive, young
Organism Mus musculus
Characteristics strain/background: SJL-ChrY^B10.S
gender: male
age: ≤ 4 weeks
cell type: CD4+TCRB+ cells
cell purification: FACS
Extracted molecule total RNA
Extraction protocol RNA was isolated from live cells using the Qiagen RNeasy® Plus Mini Kit following the manufacturer's instructions (Qiagen, Valencia, CA).
Label Biotin
Label protocol Oligonucleotide microarray analysis of RNA expression levels was performed in the Vermont Genetics Network Microarray Facility using the Affymetrix GeneChip Platform (Affymetrix Inc., Santa Clara, CA) according to manufacturer's protocols. In brief, the Nugen Ovation system v.2 with SPIA® RNA amplification was employed to convert 50ng of total RNA to cDNA. This isothermal RNA amplification system produces 5-12 ug of anti-sense cDNA targets that is followed by several steps to produce sense strand cDNA to be fragmented, biotinylated and hybridized to the GeneChip.
 
Hybridization protocol After purification and fragmentation, biotinylated-cDNA targets were hybridized to the Mouse Gene 1.0 ST Arrays oligonucleotide arrays for 16 hours at 45oC. Hybridized arrays were washed and stained with streptavidin-phycoerythrin followed by sequential incubations with biotin-coupled polyclonal anti-streptavidin antibody and streptavidin phycoerythrin as a fluorescent amplification step.
Scan protocol After staining, arrays were scanned (3000-7G Scanner, Affymetrix Inc., Santa Clara, CA) and data collected for statistical analysis.
Description YY4#1
Data processing Raw GeneChip data (one DAT file for each chip) includes a collection of images, one for each probe and chip. Each image was summarized by Affymetrix GCOS software using one probe intensity (in CEL files, one per chip).sample.
Information from multiple probes was combined to obtain a single measure of expression for each probe set and sample. Probe-level intensities were calculated using the Robust Multichip Average (RMA) algorithm, including background-correction, normalization (quantile), and summarization (median polish), for each probe set and sample, as is implemented in Partek Genomic Suites®, version 6.6 (Copyright © 2009, Partek Inc., St. Louis, MO, USA).
probe group file: MoGene-1_0-st-v1.r4.pgf
meta-probeset file: MoGene-1_0-st-v1.na32.mm9.transcript.csv
 
Submission date May 28, 2013
Last update date May 28, 2013
Contact name Laure Case
E-mail(s) [email protected]
Organization name University of Vermont
Street address 89 Beaumont Ave
City Burlington
ZIP/Postal code 05405
Country USA
 
Platform ID GPL10740
Series (2)
GSE47437 Lymph node CD4+ T cell and thioglycollate-elicited peritoneal macrophage expression data from naïve young and old SJL/J and SJL-ChrY^B10.S male mice
GSE47440 The Y chromosome as a regulatory element shaping immune cell transcriptomes and susceptibility to autoimmune disease

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
10338001 12.7089
10338002 4.44054
10338003 11.1238
10338004 10.1641
10338005 2.02628
10338006 2.16279
10338007 2.35513
10338008 2.71828
10338009 5.25476
10338010 2.09364
10338011 3.90124
10338012 2.08854
10338013 2.00094
10338014 1.98958
10338015 1.96587
10338016 4.87685
10338017 13.1338
10338018 4.63051
10338019 3.58347
10338020 5.56985

Total number of rows: 65529

Table truncated, full table size 1080 Kbytes.




Supplementary file Size Download File type/resource
GSM1149525_YY4_1-Teuscher-3-23-2012-Pico_Ovation_Exon-9.9.CEL.gz 3.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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