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NU1 cells Chipseq data
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创建时间：
2025-05-20
相关数据集
Investigation of Rap1 binding occupancy in global H3-depletion condition [Rap1_ChIPseq]. Investigation of Rap1 binding occupancy in global H3-depletion condition [Rap1_ChIPseq]
We constructed the inducible H3-depleted and FLAG-tag of the repressor activator protein 1 (Rap1) yeasts to investigate the depleted effect of nucleosomal H3 on DNA-binding profiles of Rap1 and result
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Genome-wide maps of chromatin state in PANC-1 cells.
To investigate functional associations between SIRT1 and CUL4B, we used ChIP-seq to analyze genome-wide SIRT1/CUL4B complex transcriptional targets. ChIP experiments were performed first in PANC-1 ce
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Mint-ChIP-seq from activated T-helper 17 cell (ENCSR989FGD)
For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov/Pages/Research/ENCODE/ENCODE_Data_Use_Policy_for_External_Users_03-07-14.pdf https://www.e
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Mapping ERβ genomic binding sites reveals unique genomic features and identifies EBF1 as an ERβ interactor [Gro-Seq]. Homo sapiens
The C4-12/Flag.ERβ cell line which stably expressed Flag.ERβ is used to study ERβ genomic functions without ERα interference. Mapping ERβ binding sites in these cells reveals ERβ unique distribution a
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