NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2837636 Query DataSets for GSM2837636
Status Public on May 21, 2019
Title DLD1 siUHRF1-1 plus TSA
Sample type genomic
 
Source name DLD1 with UHRF1 siRNA1 plus TSA
Organism Homo sapiens
Characteristics cell line: DLD1
sirna: UHRF1 siRNA1
genotype: UHRF1 depletion
agent: Trichostatin A
Treatment protocol DLD1 cells were transfected with a control siRNA (Thermo Fisher Scientific) or siRNAs targeting UHRF1 (Thermo Fisher Scientific) using using Lipofectamine RNAiMAX (Thermo Fisher Scientific) and incubated for 48 h. Cells were then treated with mock (ethanol) or 300 nM Trichostatin A (TSA) for additional 24 h.
Growth protocol DLD1 cells were cultured in DMEM supplemented with 10% heat-inactivated fetal bovine serum. The cultures were incubated at 37 ÂșC in a humidified incubator with 5% CO2.
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was extracted using the standard phenol-chloroform method.
Label Cy5 and Cy3
Label protocol Standard Illumina Protocol
 
Hybridization protocol Bisulphite converted DNA was amplified, fragmented and hybridized to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol.
Scan protocol Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting.
Description 9682764154_R05C01_Grn.idat
9682764154_R05C01_Red.idat
DLD1 with UHRF1 siRNA1 plus TSA
DLD1-siUHRF1-1-TSA
Data processing BeadStudio software V2011.1
Signals were background subtracted and normalized to internal controls using GenomeStudio V2011.1 and Methylation Module 1.9.0.
 
Submission date Nov 02, 2017
Last update date May 21, 2019
Contact name Hiromu Suzuki
E-mail(s) hsuzuki@sapmed.ac.jp
Phone +81-11-611-2111
Organization name Sapporo Medical University
Department Department of Molecular Biology
Street address S1, W17, Chuo-ku
City Sapporo
State/province Hokkaido
ZIP/Postal code 060-8556
Country Japan
 
Platform ID GPL13534
Series (2)
GSE106437 Analysis of DNA methylation in colorectal cancer DLD1 cells with UHRF1 depletion and HDAC inhibition
GSE106439 UHRF1 depletion and HDAC inhibition synergistically reactivate epigenetically silenced genes in colorectal cancer cells

Data table header descriptions
ID_REF
VALUE Average Beta (normalized)
Detection Pval

Data table
ID_REF VALUE Detection Pval
cg00000029 0.2857 0
cg00000108 0.81364 0
cg00000109 0.50791 0
cg00000165 0.37995 0
cg00000236 0.43197 0
cg00000289 0.40777 0
cg00000292 0.4646 0
cg00000321 0.46438 0
cg00000363 0.5809 0
cg00000622 0.01055 0
cg00000658 0.58731 0
cg00000714 0.11223 0
cg00000721 0.62365 0
cg00000734 0.07643 0
cg00000769 0.05866 0
cg00000807 0.43261 0
cg00000884 0.69926 0
cg00000905 0.06588 0
cg00000924 0.46665 0
cg00000948 0.55463 0

Total number of rows: 485577

Table truncated, full table size 9902 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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