NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM898710 Query DataSets for GSM898710
Status Public on Mar 22, 2012
Title BEAS-2B_Contrl_Clone_rep_1
Sample type RNA
 
Source name agar-derived clone_not treated_paired with As and Ni clones
Organism Homo sapiens
Characteristics cell line background: BEAS-2B
background cell type: immortalized human bronchial epithelial cell
cell type: agar-derived control clone
Treatment protocol Cells were treated with an aqueous filter-sterlized solution of metals at the concentrations and days indicated prior to seeding in soft agar; metal was removed before seeding in soft agar and for the remainder of the experiment.
Growth protocol cell were grown under standard laboratory conditions in DMEM supplemented with 10% FBS and 1% PenStrep; a single cell suspension of 5,000 cells per 9.6 square cm was seeded in soft agar at a concentration of 0.35%
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using Trizol (Invitrogen) according to the manufacturer’s protocol and purified using RNeasy Plus Micro Kit (Qiagen).
Label biotin
Label protocol The cDNA probes were synthesized using the WT Expression Kit for Affymetrix Whole Transcript Expression Arrays (Ambion), fragmented, and labeled using Affymetrix Whole Transcript Terminal Labeling Kit (Affymetrix).
 
Hybridization protocol cRNA generated by the labeling procedure was hybridized for 16 hr to the Affymetrix array according to the manufacturer's manual. Genechips were processed using protocol FS450_0007 for Genechip® fluidics station 450.
Scan protocol Affymetrix GeneArray scanner 7G
Description Ctrl-1
Data processing Feature intensity was extracted by GeneChip Operating System as CEL files; data from cel files were batch normalized in R using the COMBAT package. The probe-level analysis of the batch-normalized data was done by the RMA-16 algorithm using GeneSpring GX11.5 program.
 
Submission date Mar 21, 2012
Last update date Sep 01, 2016
Contact name Hailey A. Clancy
E-mail(s) [email protected]
Phone (845) 731-3592
Organization name New York University
Department Environmental Medicine
Lab Dr. Max Costa
Street address 57 Old Forge Road
City Tuxedo
State/province NY
ZIP/Postal code 10987
Country USA
 
Platform ID GPL6244
Series (1)
GSE36684 Exposure of an immortalized human bronchial epithelial cell line, BEAS-2B, to one of four metals (arsenic, chromium, nickel or vanadium) to determine the early changes that lead to cell transformation
Relations
Reanalyzed by GSE86357

Data table header descriptions
ID_REF
VALUE normalized

Data table
ID_REF VALUE
7892501 6.86199585
7892502 6.001509963
7892503 4.485570785
7892504 9.347539376
7892505 3.642212296
7892506 6.524415013
7892507 6.231275826
7892508 7.186794998
7892509 12.43815848
7892510 6.081777246
7892511 4.367015219
7892512 7.600365474
7892513 4.782591392
7892514 11.47256824
7892515 9.393498795
7892516 7.321110188
7892517 7.974667131
7892518 4.095127421
7892519 5.811856184
7892520 9.464717746

Total number of rows: 32321

Table truncated, full table size 627 Kbytes.




Supplementary file Size Download File type/resource
GSM898710_C1.CEL.gz 4.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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