|
Status |
Public on Dec 31, 2014 |
Title |
DNA methylation in HCT116 |
Sample type |
genomic |
|
|
Source name |
Cell line
|
Organism |
Homo sapiens |
Characteristics |
cell line: HCT116
|
Growth protocol |
Du145, PC3, MCF7, MDA-MB-231, and RKO were maintained in RPMI1640 medium. HCT116 was maintained in McCoy's 5A medium. RWPE1 was maintained in keratinocyte-SFM. HMEC was maintained in mammary epithelial cell serum-free growth medium. FHC was maintained in mixture of Ham's F12 and DMEM (1:1).
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Genomic DNA was extracted by standard phenol/chloroform method, and was quantified using a Quant-iT PicoGreen dsDNA Assay Kit (Life Technologies).
|
Label |
Cy5 and Cy3
|
Label protocol |
Standard Illumina Protocol
|
|
|
Hybridization protocol |
Standard Illumina Protocol
|
Scan protocol |
The array was scanned with an iScan System.
|
Description |
Cancer cell line
|
Data processing |
The data were analyzed using GenomeStudio Methylation Module Software.
|
|
|
Submission date |
Feb 06, 2014 |
Last update date |
Dec 31, 2014 |
Contact name |
Hideyuki Takeshima |
E-mail(s) |
takeshima.hideyuki@hoshi.ac.jp
|
Organization name |
Hoshi University
|
Department |
Institute for Advanced Life Sciences
|
Lab |
Department of Epigenomics
|
Street address |
2-4-41 Ebara
|
City |
Shinagawa-ku |
State/province |
Tokyo |
ZIP/Postal code |
142-8501 |
Country |
Japan |
|
|
Platform ID |
GPL13534 |
Series (1) |
GSE54758 |
DNA methylation, H3K27me3, and gene expression statuses of human cancer cell lines and normal cells. |
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