Experiment summary for ENCSR452GUC

doi:10.17989/ENCSR452GUC

Summary

Status
released
Assay
ChIP-seq (Control ChIP-seq)
Control type
input library
Biosample summary
Homo sapiens BLaER1 120 hours after the sample was treated with 100 nM 17β-estradiol, 10 ng/mL Interleukin-3, 10 ng/mL CSF1
Biosample Type
cell line
Replication type
isogenic
Description
Control ChIP-Seq on BLaER1 cell line after 120 h treatment with 100 nM 17β-estradiol, 10 ng/mL Interleukin-3, 10 ng/mL CSF1.
Treatments
100 nM 17β-estradiol (CHEBI:16469) , 10 ng/mL Interleukin-3 (UniProtKB:P08700) , 10 ng/mL CSF1 (UniProtKB:P09603)
Nucleic acid type
DNA
Average fragment size
527 [1-1]326 [2-1]
Fragmentation methods
shearing (Covaris generic)
Size selection method
AMPure XP bead purification

Attribution

Community submission
Lab
Roderic Guigo, CRG
Award
ERC-2011-AdG-294653-RNA-MAPS (Roderic Guigo, CRG)
Project
community
External resources
Aliases
roderic-guigo:td_chipseq_H120InputX_experiment
Date released
May 10, 2022

Isogenic replicates

Isogenic replicate
Technical replicate
Summary
Biosample
Library
11Homo sapiens BLaER1 cell line 120 hours after the sample was treated with 100 nM 17β-estradiol, 10 ng/mL Interleukin-3, 10 ng/mL CSF1ENCBS019UMZENCLB156ECT
21Homo sapiens BLaER1 cell line 120 hours after the sample was treated with 100 nM 17β-estradiol, 10 ng/mL Interleukin-3, 10 ng/mL CSF1ENCBS040UGCENCLB066ZDY