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Sample GSM1011495 Query DataSets for GSM1011495
Status Public on Sep 30, 2012
Title Foxp3-GFP spleen CD4+ non-Treg, biological rep 3
Sample type RNA
 
Source name healthy spleen CD4+ non-Treg
Organism Mus musculus
Characteristics tissue: spleen
genetic background: C57BL/6
genotype: Foxp3-GFP
age: 4 months old
gender: male
Treatment protocol Mice were sacraficed and organs were harvested. For polyp-ridden APC mice, small intestine polyps were microdisected from health surrounding tissue; both parts were used as a source of mononuclear cells. Mononuclear cells from small intestine tissue were isolated by collengenase IV digestion and precoll gradient centrifugation. Cells from spleen and mesenteric lymph nodes were isolated by gentlely teasing between frosted glass slides. Spleen cells were subjected to red blood cell lysis. Negative selection with T-cell negative selection kit (Dynal beads; Invitrogen) was used to pre-purify cells. Cells were Pc blocked and then stained with CD4 antibody. PI was used to exclude dead cells during FACS sorting. Cells were then double sorted on a MoFlo sorter. A doublet exclusion gate was included. Cells were then gated on PI negative, CD4+ cells. Two populations were then collected directly into Trizol: CD4+Foxpe-GFP- and CD4+Foxp3-GFP+. Cell isolation and sorting were performed according to immgen.org SOP.
Extracted molecule total RNA
Extraction protocol Trizol
Label biotin
Label protocol Affymetrix GeneChip WT Sense Target Labeling and Control Reagents
 
Hybridization protocol Affymetrix GeneChip WT cDNA Synthesis and Amplification Kits
Scan protocol Affymetrix GeneChip Scanner
Data processing The datasets were pre-filtered to keep only those probesets for which a gene symbol could be found in the affymetrix annotation. CEL files were normalized using Affymetrix Power tools on the predefined probeset ID list mentioned above, and using the standard RMA workflow (background adjustment, quantiile normalization, median polish probeset summarization).
 
Submission date Sep 29, 2012
Last update date Sep 30, 2012
Contact name Nichole Blatner
E-mail(s) [email protected]
Phone 312-503-1905
Fax 312-503-0386
Organization name Northwestern University
Department Robert H. Lurie Comprehensive Cancer Center
Lab Khazaie Lab
Street address 303 East Superior Street, Lurie 3-250
City Chicago
State/province IL
ZIP/Postal code 60611
Country USA
 
Platform ID GPL6246
Series (1)
GSE41229 Expression data from T-cells isolated from healthy mice or mice with polyposis

Data table header descriptions
ID_REF
VALUE RMA-normalized signal intensity

Data table
ID_REF VALUE
10344620 29.5067
10344622 199.947
10344624 806.5358
10344633 695.3783
10344637 250.6572
10344653 24.9257
10344658 350.7411
10344674 21.4268
10344679 44.439
10344707 446.3219
10344713 516.0049
10344719 113.9386
10344723 54.0387
10344725 54.1817
10344743 45.2367
10344750 208.7004
10344772 44.8697
10344789 169.6718
10344797 393.4234
10344799 308.8437

Total number of rows: 25194

Table truncated, full table size 432 Kbytes.




Supplementary file Size Download File type/resource
GSM1011495_EA07068_145450_MOGENE-1_0-ST-V1_B6.SPL.FOXP3+_1.CEL.gz 4.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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