Experiment summary for ENCSR566AUD

doi:10.17989/ENCSR566AUD

Summary

Status
released
Assay
ChIP-seq (Control ChIP-seq)
Control type
input library
Biosample summary
Homo sapiens BLaER1 6 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 6 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
338 [2-1]336 [1-1]
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_H006InputX_experiment
Date released
May 10, 2022

Isogenic replicates

Isogenic replicate
Technical replicate
Summary
Biosample
Library
21Homo sapiens BLaER1 cell line 6 hours after the sample was treated with 100 nM 17β-estradiol, 10 ng/mL Interleukin-3, 10 ng/mL CSF1ENCBS411JBCENCLB240IKT
11Homo sapiens BLaER1 cell line 6 hours after the sample was treated with 100 nM 17β-estradiol, 10 ng/mL Interleukin-3, 10 ng/mL CSF1ENCBS584ALJENCLB478MSM