NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM898730 Query DataSets for GSM898730
Status Public on Mar 22, 2012
Title BEAS-2B_Ni-transformed_Clone_rep_3
Sample type RNA
 
Source name 250.0uM NiSO4_60 days_metal removed_clone isolated from agar (4 wks)_grown in monolayer (3 wks)
Organism Homo sapiens
Characteristics cell line background: BEAS-2B
background cell type: immortalized human bronchial epithelial cell
cell type: clone isolated from agar (4 wks) and grown in monolayer (3 wks)
exposed to: 250.0uM NiSO4 for 60 days
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 Ni-3
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 7.219900264
7892502 5.952149964
7892503 4.82253755
7892504 9.324823265
7892505 4.182389227
7892506 7.010437198
7892507 6.624842145
7892508 5.698427609
7892509 12.63271329
7892510 5.847446211
7892511 4.522496467
7892512 8.06768288
7892513 4.805866304
7892514 11.55612612
7892515 9.355766905
7892516 6.771093668
7892517 7.656058302
7892518 3.584704078
7892519 5.27868026
7892520 9.657525306

Total number of rows: 32321

Table truncated, full table size 627 Kbytes.




Supplementary file Size Download File type/resource
GSM898730_Ni3.CEL.gz 4.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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