NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1075003 Query DataSets for GSM1075003
Status Public on Mar 07, 2013
Title repeat Tgfb+Il6_52hrwIL23_HJ
Sample type RNA
 
Source name Th17 cells
Organism Mus musculus
Characteristics time (hr): 52
treatment: Tgfb+Il6+Il23
cell type: Th17
Treatment protocol For Th17 differentiation: 2ng/mL rhTGF-β1 (Miltenyi Biotec), 25ng/mL rmIl-6 (Miltenyi Biotec), 20ng/ml rmIl-23 (Miltenyi Biotec), and 20ng/ml rmIL-β1 (Miltenyi Biotec). Cells were cultured for 48 hours.
Growth protocol Cd4+ T cells were purified from spleen and lymph nodes using anti-CD4 microbeads (Miltenyi Biotech) then stained in PBS with 1% FCS for 20 min at room temperature with anti-Cd4-PerCP, anti-Cd62l-APC, and anti-Cd44-PE antibodies (all Biolegend, CA). Naïve Cd4+ Cd62lhigh Cd44low T cells were sorted using the BD FACSAria cell sorter. Sorted cells were activated with plate bound anti-Cd3 (2μg/ml) and anti-Cd28 (2μg/ml) in the presence of cytokines.
Extracted molecule total RNA
Extraction protocol Extraction of total RNA was performed according to the RNeasy Mini Kit (Qiagen) manufacturer's instructions.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 100 ng total RNA (3' IVT Express Kit, Affymetrix).
 
Hybridization protocol Following fragmentation, 12.5 ug of cRNA were hybridized for 16 hr at 45C on Affymetrix microarray HT_MG-430A. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner 3000 7G
Data processing Expression data was preprocessed using the RMA algorithm followed by quantile normalization, with the parameters in the ExpressionFileCreator module of the GenePattern suite set to default
 
Submission date Jan 31, 2013
Last update date Mar 07, 2013
Contact name Nir Yosef
E-mail(s) niryosef@berkeley.edu
Phone (617) 714-7734
Organization name UC Berkeley
Department EECS
Lab Yosef
Street address Berkeley
City Berkeley
State/province CA
ZIP/Postal code 94720
Country USA
 
Platform ID GPL8321
Series (2)
GSE43955 Reconstruction of the dynamic regulatory network that controls Th17 cell differentiation by systematic perturbation in primary cells (Th17 differentiation timecourse)
GSE43970 Reconstruction of the dynamic regulatory network that controls Th17 cell differentiation by systematic perturbation in primary cells

Data table header descriptions
ID_REF
VALUE RMA normalized signal

Data table
ID_REF VALUE
1415670_at 780.6996904
1415671_at 663.9259081
1415672_at 1914.467288
1415673_at 1223.478003
1415674_a_at 988.0529292
1415675_at 679.9679954
1415676_a_at 3568.650459
1415677_at 213.1668964
1415678_at 684.3699797
1415679_at 1654.257459
1415680_at 761.547156
1415681_at 896.8663855
1415682_at 414.121107
1415683_at 2150.318963
1415684_at 243.425623
1415685_at 513.9393503
1415686_at 488.6101243
1415687_a_at 927.4702506
1415688_at 801.6834936
1415689_s_at 206.7817538

Total number of rows: 22690

Table truncated, full table size 521 Kbytes.




Supplementary file Size Download File type/resource
GSM1075003_APPLY_p_Hulin_58_430A_Mouse430A_2_E09_528236.EXPRESSION.CEL.gz 1.9 Mb (ftp)(http) CEL
Processed data included within Sample table

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