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Sample GSM365915 Query DataSets for GSM365915
Status Public on Jan 31, 2009
Title CD4 T sells, Self Antigen, Rep 1
Sample type RNA
 
Source name Self-antigen model (C3HA)
Organism Mus musculus
Characteristics B10.d2, Male,CFSE-diluted , Self-antigen activated CD4 T cell
Treatment protocol HA-specific CD4 T that had undergone antigen specific division in vivo (i.e. CFSE-diluted)cells were harvested from lymph nodes 3-7 days post adoptive transfer. FACSVantage SE cell sorter (BD Biosciences) was used to sort T cells by gating on CFSE-diluted and Thy1.1+ (donor origin) from enriched CD4 T cells
Growth protocol CFSE labeled TCR transgenic CD4 T cells specific for HA were harvested from donor mice, purified using Miltenyi’s magnetically labeled beads, and adoptively transferred into tumor-antigen recognition model (ProHA x TRAMP), Self-antigen recognition model (C3HA), viral-antigen recognition model (VaccHA) activation control, and naïve adoptive transfer control (Nontrangenic) mice
Extracted molecule total RNA
Extraction protocol Sorted cells were pelleted suspended in Trizol and stored at -80ºC prior to RNA extraction using the Trizol reagent according to the manufacturer's instructions. RNA integrity was analyzed using an Agilent 2100 Bioanalyzer, the RNA 6000 Pico, and Nano Kits (Agilent Technologies).
Label Biotin
Label protocol Standard labeling following the manufacturers protocol was carried out after cDNA was synthesized using the Nugen FL-Ovation cDNA Biotin Module V2 kit, (http://www.nugeninc.com/pdfs/flbv2_userguide.pdf).
 
Hybridization protocol Samples were hybridized to separate Affymetrix Mouse 430 Plus2 expression array chips
Scan protocol Expression array Chips were scanned using Affymetrix GeneChip Scanner 3000
Description Gene Expression Profile of a T cell responding to self
CDra-TTT-HA-1a-MOE430_2 [C3HA]
Data processing Relative expression levels were calculated using the MAS5.0 normalization
 
Submission date Jan 30, 2009
Last update date Aug 28, 2018
Contact name Charles G Drake
E-mail(s) drakech@jhmi.edu
Phone (410) 502-7523
Fax (443) 287-4653
Organization name Johns Hopkins Sidney Kimmel Comprehensive Cancer Center
Department Department of Oncology
Lab Immunology
Street address 1650 Orleans St CRB I #410
City Baltimore
State/province MD
ZIP/Postal code 21231
Country USA
 
Platform ID GPL1261
Series (1)
GSE14662 Tumor and Self-Recognition Induce Distinct Transcriptional Profiles in Antigen-Specific CD4 T Cells
Relations
Reanalyzed by GSE119085

Data table header descriptions
ID_REF
VALUE MAS5.0 Signal intensity
ABS_CALL
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 593.7 P 0.000857
AFFX-BioB-M_at 926.9 P 0.000044
AFFX-BioB-3_at 610.2 P 0.000044
AFFX-BioC-5_at 1415.7 P 0.000095
AFFX-BioC-3_at 1189.3 P 0.000044
AFFX-BioDn-5_at 1422.5 P 0.000044
AFFX-BioDn-3_at 6589.8 P 0.000052
AFFX-CreX-5_at 19499.8 P 0.000044
AFFX-CreX-3_at 21406.6 P 0.000044
AFFX-DapX-5_at 33.6 A 0.205732
AFFX-DapX-M_at 48 A 0.123572
AFFX-DapX-3_at 3.7 A 0.988616
AFFX-LysX-5_at 2.9 A 0.672921
AFFX-LysX-M_at 22.4 A 0.737173
AFFX-LysX-3_at 19.4 A 0.300606
AFFX-PheX-5_at 4.2 A 0.910522
AFFX-PheX-M_at 3.5 A 0.883887
AFFX-PheX-3_at 23.7 A 0.58862
AFFX-ThrX-5_at 8.5 A 0.760937
AFFX-ThrX-M_at 61.5 A 0.175328

Total number of rows: 45101

Table truncated, full table size 1204 Kbytes.




Supplementary file Size Download File type/resource
GSM365915.CEL.gz 3.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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