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Sample GSM1537225 Query DataSets for GSM1537225
Status Public on Dec 25, 2015
Title Naive T cells_002
Sample type RNA
 
Source name Naive mouse
Organism Mus musculus
Characteristics strain: C57Bl/6
gender: female
tissue: spleen
sorting parameters: Naive T cells: CD8-, B220-, CD4+, CD44-, CD62L+
Treatment protocol Mice were immunised with sheep red blood cells (2x10^9 i.p.) or S. enterica (10^6 colony forming units of SL3261 strain, i.v.). Mice were left untreated for 6 days, at which point spleens were harvested for analysis.
Red blood cells were lysed with RBC lysis buffer. Splenocytes were enriched in CD4+ T cells by negative selection with Dynabeads (Invitrogen). Cells were then stained for flow cytometry and sorted over BD Aria flow cytometer sorter based on the expression of surface markers as described in the table.
Extracted molecule total RNA
Extraction protocol RNA was extracted by passing TRIZOL over Qiagen Rneasy columns as per manufacturer's instructions.
Label biotin
Label protocol RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 100-300ng of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol.
 
Hybridization protocol cRNA was hybridized to Affymetrix Mouse Gene 1.1 ST Arrays according to manufacturer’s protocol.
Scan protocol Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol.
Data processing Data were processed using rma and limma packages in R/Bioconductor. Pairwise group comparisons were undertaken using linear modelling. Subsequently, empirical Bayesian analysis was applied, including vertical (within a given comparison) p value adjustment for multiple testing, which controls for false discovery rate, using the limma Bioconductor package
The normalised data are log2 values for the probes reliably detected on all arrays, processed using rma followed by quantile normalisation.
 
Submission date Nov 04, 2014
Last update date Dec 25, 2015
Contact name Alasdair Ivens
E-mail(s) al.ivens@ed.ac.uk
Phone 44 131 6513605
Organization name Centre for Immunity, Infection and Evolution
Street address Kings Buildings
City Edinburgh
ZIP/Postal code EH9 3FL
Country United Kingdom
 
Platform ID GPL17997
Series (1)
GSE62961 Investigating heterogeneity within T follicular helper cells (TFH) population.

Data table header descriptions
ID_REF
VALUE log2 normalized signal

Data table
ID_REF VALUE
100009600_at 3.376
100009609_at 2.5534
100012_at 2.4161
100017_at 6.9968
100019_at 8.2499
100033459_at 8.6856
100034251_at 3.4539
100036521_at 5.555
100037258_at 9.7315
100037278_at 4.8396
100038380_at 3.8467
100038429_at 3.9951
100038486_at 3.0718
100038570_at 3.3587
100038598_at 3.1106
100038600_at 4.3878
100038618_at 6.424
100038635_at 4.9715
100038680_at 3.9054
100038683_at 2.9876

Total number of rows: 21212

Table truncated, full table size 339 Kbytes.




Supplementary file Size Download File type/resource
GSM1537225_Titan_0049_754M_Gray_754M_002_H07.CEL.gz 3.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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