|
Status |
Public on Jun 17, 2020 |
Title |
MTF1-Null_Suloctidil_rep1_P-5_E03 |
Sample type |
SRA |
|
|
Source name |
MCF-7 cells
|
Organism |
Homo sapiens |
Characteristics |
chemical: Suloctidil dose (um): 10
|
Treatment protocol |
Chemicals, purchased from Sigma-Aldrich, were ≥ 95% pure. All chemical stock solutions were made in DMSO. After a 48 hour incubation, MCF-7 cells were exposed for 6 hours to DMSO (0.05%) or one of the six test chemicals in DMSO (final concentration 0.05%) at a concentration of 1-100 uM. Media was removed and cells were lysed in 0.5 mL Trizol.
|
Growth protocol |
MCF-7 cells were cultured in DMEM media (GIBCO) supplemented with 10% FBS (Omega Scientific, Australia) and 1x penicillin/streptomycin/glutamine. Cells were plated at 15 x10^5 cells per well in 12-well plates and cultured for 48 hours and then exposed to test chemicals for 6 hours.
|
Extracted molecule |
total RNA |
Extraction protocol |
After cells were lysed in 0.5 mL Trizol, total RNA was extracted from each lysate and prepared for gene expression analysis using the human 1500+ Tempo-Seq platform (BioSpyder, Inc, Carlsbad, CA).
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
TempO-Seq data are analyzed using the Tempo-SeqR software package which uses the statistical computing language R. The input data analyzed was taken from the FASTQ files. Each file was aligned to a pseudo-transcriptome input using the Bowtie algorithm. The data analysis output is a table of counts with each column representing a sample and each row representing a gene. Supplementary_files_format_and_content: counts
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|
|
Submission date |
Jun 17, 2020 |
Last update date |
Jun 18, 2020 |
Contact name |
Christopher Corton |
E-mail(s) |
[email protected]
|
Organization name |
US-EPA
|
Lab |
MD B105-01
|
Street address |
109 TW Alexander Dr.
|
City |
Research Triangle Park |
State/province |
NC |
ZIP/Postal code |
27711 |
Country |
USA |
|
|
Platform ID |
GPL11154 |
Series (1) |
GSE152703 |
Transcript profiling of putative MTF-1 activating chemicals in wild-type and MTF-1-null MCF-7 cells |
|
Relations |
BioSample |
SAMN15300302 |
SRA |
SRX8567992 |