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Sample GSM1103574 Query DataSets for GSM1103574
Status Public on Jun 01, 2013
Title Foxp3+ ex vivo_Polysome-associated RNA_2
Sample type RNA
 
Source name Cells isolated from lymph nodes and spleens
Organism Mus musculus
Characteristics strain: C57BL/6
cell type: Foxp3+
condition: Ex vivo
isolated rna: Polysome-associated RNA
Treatment protocol For the naïve cells all buffers and media were supplemented with cycloheximide (Sigma, St. Louis, MO) (100µg/ml). For the activated samples cells were activated for 36h with plate bound CD3 and CD28 antibodies (BD Bioscience) (5µg/ml) in the presence of recombinant hIL-2 ([100U/ml]
Growth protocol Cells isolated from lymph nodes and spleens were stained with PE conjugated CD4 antibody (GK1.5, eBioscience, San Diego, CA) and MACS purified. Thereafter TFoxp3+ and TFoxp3- cells were sorted based on CD4 and GFP-Foxp3 expression using a FACSAria to obtain cell populations of high purity (>97%). For the activated samples cells were activated for 36h with plate bound CD3 and CD28 antibodies (BD Bioscience) (5µg/ml) in the presence of recombinant hIL-2 ([100U/ml]
Extracted molecule total RNA
Extraction protocol Cytosolic and polysome-associated RNA were prepared directly ex vivo or post-activation in vitro as described previously (Larsson O, 2007 ancer Res 67: 6814-6824). For cells isolated directly ex vivo, RNA from two experiments was pooled for each sample.
Label biotin
Label protocol Ovation Pico WTA system (NuGEN) according to the manufacturer’s instructions.
 
Hybridization protocol Samples were hybridized with the Affymetrix GeneChip Mouse Genome 430 2.0 Array according the instructions of the manufacturer
Scan protocol Arrays were scanned using the GeneArray Scanner 3000 according to the instructions from the manufacturer.
Description Gene expression data from Foxp3+ cells Ex vivo using RNA isolated from Polysome-associated RNA
YV090709CPO072-2_01.CEL
Data processing Data were extracted and normalized using a custom CDF and Robust Multi-array Average (RMA) in R (r-project.org) with default settings.
 
Submission date Mar 21, 2013
Last update date Jun 01, 2013
Contact name Ola Larsson
E-mail(s) ola.larsson@ki.se
Phone +46 (0)8 517 73280
Organization name Karolinska Institutet
Department Department of oncology-pathology
Street address CCK, R8:01
City Stockholm
ZIP/Postal code 171 76
Country Sweden
 
Platform ID GPL7546
Series (1)
GSE45401 Distinct translational control in CD4+ T-cell subsets

Data table header descriptions
ID_REF
VALUE Log2 RMA signal

Data table
ID_REF VALUE
100009600_at 5.032214444
100012_at 2.69545551
100017_at 11.15275197
100019_at 6.411791148
100034251_at 5.284100998
100036521_at 2.5507182
100037258_at 6.03364676
100037278_at 5.988577915
100038570_at 4.53677298
100038635_at 3.493914574
100038680_at 4.903851547
100038887_at 9.514301822
100038959_at 7.319160407
100039026_at 5.324499106
100039027_at 3.328386666
100039094_at 4.231690562
100039235_at 5.894777096
100039282_at 2.276794317
100039284_at 5.640863416
100039307_at 4.539193302

Total number of rows: 16539

Table truncated, full table size 343 Kbytes.




Supplementary file Size Download File type/resource
GSM1103574_YV090709CPO072-2_01.CEL.gz 3.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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