NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM861112 Query DataSets for GSM861112
Status Public on Jan 13, 2012
Title hSFC BPA 10nM 24h Cell 1
Sample type RNA
 
Source name human skin fibroblast cells, 24h, 10nM BPA, Cell1
Organism Homo sapiens
Characteristics congenital condition: hypospadias
treatment: 10 nM BPA
cell type: Skin fibroblast
gender: Male
Growth protocol hSFCs were maintained in DMEM/Ham's F-12 (048-29785, Wako, Osaka, Japan) containing 10% fetal bovine serum (FBS, Mediatech, Herndon, VA) and grown at 37°C in a 5% CO2 humidified incubator. For growth under steroid-free conditions, the cells were seeded in phenol red-free DMEM/Ham's F-12 (045-30665, Wako) containing 5% charcoal/dextran-treated FBS (Hyclone, Logan, UT). All the culture media contained 100 U/ml penicillin/streptomycin and 2 mmol/L L-glutamine (Mediatech, Herndon, VA).
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from the culture cells after treated with chemicals for 24 h using an RNeasy Kit (Qiagen, Valencia, CA) in accordancewith the manufacturer’s instructions. Quantification and quality assessment of theisolated RNA samples were performed and verified using an Agilent Bioanalyzer2100 (Agilent Technologies, Palo Alto, CA)and aNanoDrop spectrophotometer (NanoDrop products, Wilmington, DE) in accordancewith the manufacturer’s instructions.
Label Cy3
Label protocol RNA was amplified into cRNA and labeled with Agilent One-Color Microarray-Based Gene Expression Analysis protocol (Agilent Technologies).
 
Hybridization protocol Sampleswere then hybridized to the G4851A SurePrint G3 Human GE 8x60Karray slides (60000 probes, Agilent Technologies).
Scan protocol The arrays were scanned using Agilent Microarray Scanner (G2565BA, Agilent Technologies).
Description Gene expression after 24h 10nM BPA treatment
Data processing The scanned images were analyzed using the standard procedures described in Agilent Feature Extraction software 9.5.3.1 (Agilent Technologies). Data analysis was performed with GeneSpring GX12.0.2 (Agilent Technologies).
 
Submission date Jan 11, 2012
Last update date Jan 20, 2012
Contact name Sone Hideko
E-mail(s) hsone@nies.go.jp
Phone 81298502420
Organization name National Institute for Environmental Studies
Department Center for Environmental Risk Research
Lab Environmental Exposure Research Section
Street address onogawa16-2
City tsukuba
State/province ibaraki
ZIP/Postal code 305-8506
Country Japan
 
Platform ID GPL14550
Series (1)
GSE35034 Gene expression of human skin fibroblast cells derived from hypospadias patients in response to low-dose bisphenol A exposure

Data table header descriptions
ID_REF
VALUE normalized to 75th percentile of signal intensity

Data table
ID_REF VALUE
A_19_P00315452 -0.90409184
A_19_P00315459 -2.7363086
A_19_P00315469 -6.9653683
A_19_P00315473 -6.114259
A_19_P00315482 -6.0267177
A_19_P00315490 -6.851044
A_19_P00315492 -6.878698
A_19_P00315493 -4.3370442
A_19_P00315496 -7.104811
A_19_P00315499 -6.350623
A_19_P00315502 -5.7585993
A_19_P00315504 -3.3888907
A_19_P00315506 -5.375124
A_19_P00315508 -7.04763
A_19_P00315518 -6.4335585
A_19_P00315519 -7.0220656
A_19_P00315523 -1.0419378
A_19_P00315524 -3.193252
A_19_P00315526 -2.126062
A_19_P00315527 -1.9244576

Total number of rows: 42405

Table truncated, full table size 997 Kbytes.




Supplementary file Size Download File type/resource
GSM861112_1-BPA.txt.gz 12.4 Mb (ftp)(http) TXT
Processed data included within Sample table

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