|
Status |
Public on May 16, 2020 |
Title |
pkd1_input |
Sample type |
SRA |
|
|
Source name |
epithelial cells
|
Organism |
Mus musculus |
Characteristics |
tissue: Kidney cell type: pkd1(PH) chip antibody: none
|
Growth protocol |
pkd1 and null cells were cultured in DMEM-F12 medium supplemented with 3% fetal bovine serum (FBS) and 1% penicillin/streptomycin,1% Insulin-Transferrin-Selenium, IFNγ, Nystatin suspension and T3.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
pkd1 and null cells were cross-linked with 1% formaldehyde for 10 min at RT. The crosslink was stopped by adding 1/20 volume of 2.5 M glycine. Cells were washed with PBS and harvested using ChIP lysis buffer. Cells were then sonicated to obtain fragments (100-500 bp) with Bioruptor Sonicator. Immunoprecipitation was performed with H3K27ac antibody (Abcam cat# ab4729). After elution and reversal cross-linking, DNA was purified and sequenced on BGISEQ-500. Construction of ChIP-seq library was completed by BGI company (Shenzhen,China).
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
BGISEQ-500 |
|
|
Data processing |
ChIP-seq data were mapped to mus musculus genome (mm10) by SOAPaligner/SOAP2 ChIP-Seq peaks were generated using peak finding algorithm MACS (Model-based Analysis for ChIP -Seq, version: MACS-1.4.2) Reads mapped only once at locus were allowed for peak calling. Genome_build: mm10 Supplementary_files_format_and_content: Wig files were generated by MACS-1.4.2.
|
|
|
Submission date |
Dec 02, 2019 |
Last update date |
May 16, 2020 |
Contact name |
Zeyun Mi |
E-mail(s) |
mizeyun@tmu.edu.cn
|
Phone |
15900207057
|
Organization name |
Tianjin Medical University
|
Street address |
Qi Xiang Tai Road
|
City |
Tianjin |
ZIP/Postal code |
300070 |
Country |
China |
|
|
Platform ID |
GPL23479 |
Series (2) |
GSE141279 |
SE-driven metabolic reprogramming in ADPKD (ChIP-Seq) |
GSE141281 |
SE-driven metabolic reprogramming in ADPKD |
|
Relations |
BioSample |
SAMN13446748 |
SRA |
SRX7255693 |