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Sample GSM1602621 Query DataSets for GSM1602621
Status Public on Sep 18, 2015
Title TW18_D8 KO Th1_2
Sample type RNA
 
Source name Tcf7 deficient Th1 cells
Organism Mus musculus
Characteristics infection: LCMV
cell type: SMARTA CD4 Tcells
cell type (separated by facs): Th1 cells
genotype/variation: Tcf7 deficient
Treatment protocol Mice were infected with LCMV
Growth protocol NA
Extracted molecule total RNA
Extraction protocol Trizol (Invitrogen) and RNaseazy (Qiagen) kits were used to extract total RNA according to the manufacturer's instructions.
Label Biotin
Label protocol Labeling was performed on a sample-by-sample basis according to manufacturer’s guidelines for use with the Affymetrix Human HuGene-1_0-st-v1 GeneChips (Affymetrix, Inc). DNase treatment was included as part of isolation to remove possible contaminating DNA. Bioanalyzer nanochip (Agilent, Inc) and NanoDrop (ThermoFisher, Inc) were used to validate and quantitate the RNA prior to cRNA synthesis and labeling. 300 ng of total RNA was used for labeling with theAmbion WT Expression Kit (cat#4411974) and Affymetrix kit (Cat # 900652).After hybridization, the probe arrays were stained with streptavidin-phycoerythrin solution (Molecular Probes) and enhanced using an antibody solution containing 0.5 mg/mL of biotinylated anti-streptavidin (Vector Laboratories).
 
Hybridization protocol The hybridization cocktail containing the fragmented and labeled cDNAs were hybridized to Affymetrix Mouse MoGene-2_0-st microarrays. The microarrays were washed and stained in an Affymetrix Fluidics Station using standard Affymetrix protocols.
Scan protocol Genechips were scanned using an Affymetrix Gene Chip Scanner 3000.
Data processing Gene expression intensities were calculated using GeneChip Command Console Software (AGCC). .cel files generated by the Affymetrix AGCC program were imported in the Affymetrix Expression Console software and RMA (Robust Multichip Analysis) normalization was performed to generate the .chp files. The .chp files were normalized, log2 transformed, and summarized.
 
Submission date Feb 05, 2015
Last update date Sep 18, 2015
Contact name abdel G Elkahloun
E-mail(s) [email protected]
Phone 301 402 3170
Organization name NHGRI-NIH
Lab MICROARRAY CORE
Street address 50, SOUTH DRIVE
City BETHESDA
ZIP/Postal code 20892
Country USA
 
Platform ID GPL16570
Series (1)
GSE65660 TCF1 is required for the differentiation of T follicular helper (TFH) cells during viral infections

Data table header descriptions
ID_REF
VALUE log2 RMA signal

Data table
ID_REF VALUE
17200001 8.01381
17200003 8.69728
17200005 7.44181
17200007 6.8838
17200009 8.43005
17200011 7.66349
17200013 7.03545
17200015 7.30785
17200017 4.05413
17200019 5.53115
17200021 7.20989
17200023 8.49676
17200025 7.23771
17200027 7.37565
17200029 6.18267
17200031 5.37792
17200033 5.13684
17200035 4.92605
17200037 7.45187
17200039 5.3703

Total number of rows: 41345

Table truncated, full table size 681 Kbytes.




Supplementary file Size Download File type/resource
GSM1602621_TW18_D8_KO_Th1_2_MoGene-2_0-st_.CEL.gz 9.5 Mb (ftp)(http) CEL
GSM1602621_TW18_D8_KO_Th1_2_MoGene-2_0-st_.rma-gene-full.chp.gz 254.7 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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