|
Status |
Public on Jan 01, 2016 |
Title |
DNA methylation in NT cells |
Sample type |
genomic |
|
|
Source name |
Breast cancer cell line
|
Organism |
Homo sapiens |
Characteristics |
cell line: MCF7 agent: control
|
Treatment protocol |
MCF7 cells were then treated with vehicle and PJ34 for 2hours respectively.
|
Growth protocol |
Cell cultures were incubated at 37 degree with humidified air and 5% CO2. Cells were harvested after each treatment. Cells were grown ensuring that 95% of the cells were viable. Harvested cells were centrifuged for five minutes at 200 X g.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Genomic DNA was extracted using Qiagen Dneasykit according to manusfacturers instructions.
|
Label |
Cy5 and Cy3
|
Label protocol |
Standard Illumina Protocol
|
|
|
Hybridization protocol |
Bisulfite converted DNA was amplified, fragmented and hybridized to the Illumina Infinium Human Methylation450 Beadchip using the standard Illumina protocol
|
Scan protocol |
Arrays were imaged using the HiScan with the standard recommended settings
|
Description |
Sample name: MCF7
|
Data processing |
GenomeStudio v.2011.1
|
|
|
Submission date |
Sep 25, 2014 |
Last update date |
Jan 01, 2016 |
Contact name |
Yvonne Nsokika Fondufe-Mittendorf |
E-mail(s) |
y.fondufe-mittendorf@uky.edu
|
Phone |
8593230091
|
Organization name |
University of Kentucky
|
Department |
Biochemistry
|
Lab |
Mittendorf
|
Street address |
741 South Limestone dr.
|
City |
Lexington |
State/province |
KY |
ZIP/Postal code |
40536-0509 |
Country |
USA |
|
|
Platform ID |
GPL13534 |
Series (1) |
GSE61744 |
Genome-wide profiling of PARP1 reveals an interplay with gene regulatory regions and DNA methylation |
|