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Sample GSM1011477 Query DataSets for GSM1011477
Status Public on Sep 30, 2012
Title Foxp3-GFP small intestine CD4+ non-Treg, biological rep 3
Sample type RNA
 
Source name healthy small intestine CD4+ non-Treg
Organism Mus musculus
Characteristics tissue: small intestine
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 29.6432
10344622 208.7548
10344624 1131.0305
10344633 833.1424
10344637 299.378
10344653 27.8128
10344658 133.4244
10344674 25.325
10344679 72.4972
10344707 295.4529
10344713 670.1999
10344719 127.7475
10344723 45.6993
10344725 67.5414
10344743 50.2108
10344750 127.7239
10344772 42.6038
10344789 134.7864
10344797 435.727
10344799 259.252

Total number of rows: 25194

Table truncated, full table size 432 Kbytes.




Supplementary file Size Download File type/resource
GSM1011477_EA07068_222399_MOGENE-1_0-ST-V1_S.B..B6.FOXP3-.1.CEL.gz 4.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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