|
Status |
Public on Dec 08, 2018 |
Title |
ChIP-Seq p65 HeLa FLDD 0h TNF |
Sample type |
SRA |
|
|
Source name |
HeLa
|
Organism |
Homo sapiens |
Characteristics |
tissue: HeLa cells genotype/variation: p65 KO, FLDD p65 rescue tnf stimulation: 0h TNF chip antibody: p65 (C-20); Santa Cruz sc-372
|
Treatment protocol |
HeLa cells and MEFs were stimulated with TNFα (20 ng/ml) for 60 min
|
Growth protocol |
HeLa and MEF cells were cultured in DMEM (Life Technologies) supplemented with FCS and Penicillin/Streptomycin.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
For RNA-Seq cells were harvested and total RNA was isolated using the NucleoSpin RNA Kit (Macherey-Nagel). For ChIP-Seq samples were crosslinked using Formaldehyde, Sonicated and chromatin was extracted using the p65 Antibody. DNA was purified NucleoSpin Gel and PCR Clean UP Kit with buffer NTB (Macherey-Nagel). RNA-Seq libraries were prepared from total RNA using the TruSeq Stranded total RNA LT kit (Illumina). ChIP-Seq libraries were prepared from purified ChIP DNA with the Microplex Library Preparation Kit (Diagenode)
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|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 1500 |
|
|
Data processing |
ChIP-Seq data were aligned to human genome hg19 and hg38 using bowtie 1.0 with n = 1 and m = 3 as parameter
Bigwig files were created using Galaxy/Cistrome or Galaxy/deepTools, duplicated tags were ignored
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|
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Submission date |
Jun 26, 2018 |
Last update date |
Dec 08, 2018 |
Contact name |
Robert Liefke |
E-mail(s) |
[email protected]
|
Organization name |
Philipps University of Marburg
|
Department |
Institute of Molecular Biology and Tumor Research (IMT)
|
Street address |
Hans-Meerwein-Str. 2
|
City |
Marburg |
State/province |
Hessen |
ZIP/Postal code |
35043 |
Country |
Germany |
|
|
Platform ID |
GPL18460 |
Series (1) |
GSE116284 |
NF-κB p65 dimerization and DNA-binding is important for inflammatory gene expression |
|
Relations |
BioSample |
SAMN09497834 |