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Sample GSM480287 Query DataSets for GSM480287
Status Public on Jun 03, 2010
Title Subject 1188, Replicate 5
Sample type RNA
 
Source name Derived from neonatal foreskin
Organism Homo sapiens
Characteristics subject/donor: 1188
gender: Male
tissue: cultured epidermis
replicate: 5
Treatment protocol Following overnight incubation in MMM Media, individual epidermal tissues were peeled from the tissue insert and placed into 2 ml of RNAlater® (Ambion/ABI, Foster City, CA) pre-loaded into a 24-well plate. After 24 hours incubation under 4°C, the RNAlater® submersed tissues were transferred into a 2 ml Seal-Rite® microcentrifuge tube (USA Scientific Inc, Ocala, FL) and all excess RNAlater® was removed from the tissue by gentle pipetting. The tissues were stored at -80°C until RNA was isolated.
Growth protocol Reconstructed human EpiDerm™ EPI-200 tissues prepared from four different neonatal foreskin donors (254, 1188, 219 and 926) were acquired from MatTek Corporation (Ashland, MA). Five tissues from each donor were placed into 6-well plates with 1ml/tissue/well of pre-warmed (37°C) NMM media (MatTek Corp.) and incubated overnight at 37°C.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using TRI-Reagent and protocol provided by supplier (Molecular Research Center, Cincinnati, OH). Extracted RNA was further purified using Qiagen RNEasy columns and protocol provided by supplier (QIAgen, Valencia, CA).
Label biotin
Label protocol Total RNA was converted to biotin-labeled cRNA GeneChip target using Ambion Message Amp II- Biotin Enhanced Kit according to manufacture's recommendations. Biotin-labeled cRNA was purified using the Qiagen RNeasy kit and a total of 20 μg of cRNA was fragmented randomly to ~200 bp at 94°C for 35 min (200 mM Tris-acetate, pH 8.2, 500 mM KOAc, 150 mM MgOAc).
 
Hybridization protocol Following fragmentation, cRNA was hybridized for 16 hr at 45C on GeneChip Human U133plus2.0 Arrays. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner 3000.
Description Gene expression data from reconstituted human epidermis
Data processing The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1500.
 
Submission date Dec 04, 2009
Last update date Jun 02, 2010
Contact name Jay Patrick Tiesman
Organization name Procter & Gamble
Department Global Biotechnology
Lab Mason Business Center
Street address PO BOX 8006
City MASON
State/province OH
ZIP/Postal code 45040-8006
Country USA
 
Platform ID GPL570
Series (1)
GSE19330 Expression data from Epiderm cultured skin derived from four different donors

Data table header descriptions
ID_REF
VALUE Signal
ABS_CALL indicating whether the transcript was present (P), absent (A), or marginal (M)
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 258.81 A 0.262827
AFFX-BioB-M_at 227.261 A 0.195266
AFFX-BioB-3_at 22.7652 A 0.724854
AFFX-BioC-5_at 472.63 P 0.002867
AFFX-BioC-3_at 207.061 A 0.175328
AFFX-BioDn-5_at 1336.34 P 0.0020226
AFFX-BioDn-3_at 5716.37 P 0.00844047
AFFX-CreX-5_at 10026 P 7.00668e-05
AFFX-CreX-3_at 11033.6 P 4.42873e-05
AFFX-DapX-5_at 22390.6 P 4.42873e-05
AFFX-DapX-M_at 26837 P 5.16732e-05
AFFX-DapX-3_at 33562.1 P 5.16732e-05
AFFX-LysX-5_at 2343.96 P 6.02111e-05
AFFX-LysX-M_at 2772.74 P 4.42873e-05
AFFX-LysX-3_at 6075.54 P 4.42873e-05
AFFX-PheX-5_at 3858.74 P 5.16732e-05
AFFX-PheX-M_at 3975.48 P 4.42873e-05
AFFX-PheX-3_at 3871.84 P 4.42873e-05
AFFX-ThrX-5_at 2571.25 P 8.14279e-05
AFFX-ThrX-M_at 5038.79 P 4.42873e-05

Total number of rows: 54675

Table truncated, full table size 1627 Kbytes.




Supplementary file Size Download File type/resource
GSM480287.CEL.gz 4.9 Mb (ftp)(http) CEL
GSM480287.CHP.gz 291.7 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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