|
Status |
Public on Mar 22, 2012 |
Title |
BEAS-2B_Contrl_Clone_rep_11 |
Sample type |
RNA |
|
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Source name |
agar-derived clone_not treated_paired with V 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).
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|
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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-11
|
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.
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|
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Submission date |
Mar 21, 2012 |
Last update date |
Sep 01, 2016 |
Contact name |
Hailey A. Clancy |
E-mail(s) |
hah213@nyu.edu
|
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 |