ChIP-chip of E. coli K-12 MG1655 with antibody against ArgR-8myc, Lrp-8myc, and TrpR-8myc under various conditions.
Source: NCBI BioProject (ID PRJNA135559)
Source: NCBI BioProject (ID PRJNA135559)
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Project name: Escherichia coli str. K-12 substr. MG1655
Description: We integrated transcription factor binding regions and mRNA transcript abundance to elucidate the ArgR, Lrp, and TrpR regulon experimentally. To measure transcription factor binding at a genome scale, we employed a ChIP-chip method to derivative strains of E. coli K-12 MG1655 harboring ArgR-8myc, Lrp-8myc, or TrpR-8myc under various conditions.Overall design: A twelve ChIP-chip study under six separate culture conditions. The high-density oligonucleotide tiling arrays used were consisted of 371,034 oligonucleotide probes spaced 25 bp apart (25-bp overlap between two probes) across the E. coli genome.
Data type: Epigenomics
Sample scope: Multiisolate
Relevance: ModelOrganism
Organization: Systems Biology Research Group, Bioengineering, UCSD
Literatures
- PMID: 22082910
Release date: 2011-12-01
Last updated: 2010-12-14