NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM412621 Query DataSets for GSM412621
Status Public on Sep 09, 2011
Title Cells treated with medium as control, biological rep 3
Sample type RNA
 
Source name Cells treated with medium as control
Organism Homo sapiens
Characteristics tissue: Human foreskin fibroblasts (HFF) BJ
Treatment protocol Culture cells were stimulated with 5 ng/ml TGF-β1 for 3 hours in the presence or absence of T. cruzi conditioned medium.
Growth protocol 5X10^4/ml cells were seeded in in 75 mm culture plates in Dulbecco's modified Eagle medium (10%FBS,100 U/ml penicillin, 100 ug/ml streptomycin, 2mM glutamine) and allowed to grow for 48 hours at 37 C in a CO2 incubator
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions, followed by concentration using the RNeasy kit (Quiagen).
Label Biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 5 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on HG_U133 plus 2.0 GeneChips. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner 3000
Description Gene expression data from untreated human fibroblast
Data processing The raw data was uploaded into the Rosetta Resolver System for data processing and normalization using the Rosetta Resolver Affymetrix GeneChip error model (Weng et al, 2006). The expression profiles from replicate samples were combined into ratio experiments. Each gene is associated to an expression fold-change and a p-value that assesses the statistical significance of its modulation in the treated sample compared to the control reference. Sequences with absolute fold-change >=2 and p-value <= 0.01 were considered as differentially expressed.
 
Submission date Jun 03, 2009
Last update date Sep 09, 2011
Contact name Jaime Alfredo Costales
E-mail(s) [email protected], [email protected]
Organization name Pontificia Universidad Catolica del Ecuador
Department Biological Sciences
Lab Center for Infectious Disease Research
Street address 12 de Octubre y Patria
City Quito
ZIP/Postal code NN
Country Ecuador
 
Platform ID GPL570
Series (1)
GSE16416 Expression data from human primary fibroblasts treated with Trypanosoma cruzi-conditioned medium

Data table header descriptions
ID_REF
VALUE normalized signal intensity
DETECTION P-VALUE

Data table
ID_REF VALUE DETECTION P-VALUE
1007_s_at 217.11566 1.18847E-24
1053_at 230.56345 3.23599E-40
117_at 18.19252 0.02636
121_at 109.98589 3.14851E-11
1255_g_at 2.04432 0.40683
1294_at 92.14597 7.48396E-10
1316_at 36.69506 0.00015
1320_at 40.42149 0.00004
1405_i_at 12.75668 0.06207
1431_at 9.21632 0.12465
1438_at 44.62252 8.07816E-6
1487_at 105.15731 2.27962E-13
1494_f_at 19.23128 0.01766
1552256_a_at 309.18344 8.40779E-44
1552257_a_at 307.82996 3.05969E-40
1552258_at 3.13613 0.38417
1552261_at 89.67647 9.88784E-10
1552263_at 66.90161 4.87752E-10
1552264_a_at 494.85663 0
1552266_at 0.44106 0.47807

Total number of rows: 54675

Table truncated, full table size 1499 Kbytes.




Supplementary file Size Download File type/resource
GSM412621.CEL.gz 4.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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