NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1011497 Query DataSets for GSM1011497
Status Public on Sep 30, 2012
Title Foxp3-GFP small intestine CD4+ non-Treg, biological rep 6
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 45.1047
10344622 224.5933
10344624 726.5465
10344633 594.2522
10344637 298.4471
10344653 25.3259
10344658 117.4689
10344674 31.9534
10344679 48.7049
10344707 235.6004
10344713 192.3311
10344719 113.4182
10344723 63.0527
10344725 98.1304
10344743 60.0016
10344750 201.167
10344772 38.5496
10344789 88.4662
10344797 716.7636
10344799 329.8943

Total number of rows: 25194

Table truncated, full table size 433 Kbytes.




Supplementary file Size Download File type/resource
GSM1011497_EA07068_145452_MOGENE-1_0-ST-V1_B6.SB.CD4+FOXP3-_1.CEL.gz 3.6 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap