|
Status |
Public on Dec 21, 2016 |
Title |
Nrf1_ChIP-seq_MEF_replicate1 |
Sample type |
SRA |
|
|
Source name |
Wild-type MEFs immortalized with SV40 large T antigen and treated with MG132.
|
Organism |
Mus musculus |
Characteristics |
chip-antibody: Cell Signaling Technology, anti-TCF11 (D5B10) cell type: Mouse enbryonic fibroblasts
|
Treatment protocol |
MEFs were treated with 10 μM of MG132 for 6 hr.
|
Growth protocol |
MEFs were maintained in DMEM supplemented with 10% FBS and antibiotics.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Lysates were clarified from sonicated nuclei, and protein-DNA complexes were isolated using antibody to Nrf1 and Dynabeads-proteinA and -proteinG Libraries were prepared according to NuGEN's instructions accompanying the Ovation Ultralow DR Multiplex System 1-8 (NuGEN, 0330-32).
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2000 |
|
|
Description |
ChIP samples using antibody to Nrf1 obtained from MG132-treated wild-type MEFs, replicate 1
|
Data processing |
ChIP-seq reads were aligned to the mm9 genome assembly using bwa version 0.6.2-r126. Data were filtered using samtools version 0.1.18 Peaks were called using macs2 version 2.0.10 Genome_build: mm9 Supplementary_files_format_and_content: BigWig files were generated using BEDtools version 2.17.0 and UCSC Genome Bioinformatics
|
|
|
Submission date |
Oct 31, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Eri H Kobayashi |
Organization name |
Tohoku University Graduate School of Medicine
|
Department |
Medical Biochemistry
|
Street address |
2-1 Seiryo-machi, Aobaku
|
City |
Sendai |
State/province |
Miyagi |
ZIP/Postal code |
980-8575 |
Country |
Japan |
|
|
Platform ID |
GPL13112 |
Series (1) |
GSE89344 |
A Homeostatic Shift Facilitates Endoplasmic Reticulum Proteostasis through Transcriptional Integration of Proteostatic Stress Response Pathways [ChIP-seq] |
|
Relations |
BioSample |
SAMN05956186 |
SRA |
SRX2311119 |