ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR126/060/ERR12652360/ERR12652360.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR126/065/ERR12652365/ERR12652365.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR126/058/ERR12652358/ERR12652358.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR126/061/ERR12652361/ERR12652361.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR126/064/ERR12652364/ERR12652364.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR126/062/ERR12652362/ERR12652362.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR126/059/ERR12652359/ERR12652359.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR126/063/ERR12652363/ERR12652363.fastq.gzprimary200OKGenomicsUniversity of BirminghamEuropean Bioinformatics Institutehttps://www.ebi.ac.uk/ena/browser/view/PRJEB72534ArrayExpressThe experiment contains ChIP-seq data for Acinetobacter baumannii strain AB5075 encoding 3xFLAG tagged H-NS. Experiments were done with or without ectopic expression of the truncated H-NS-39 protein (corresponding to the H-NS multimerization surface). The strain was grown at 37 degrees in LB medium and crosslinked with 1 % (v/v) formaldehyde. After sonication, to break open cells and fragment DNA, immunoprecipitations were done using anti-FLAG antibodies against. Libraries were prepared using DNA remaining after immunoprecipitation.ENAfalseChIP-seq analysis of H-NS in Acinetobacter baumannii AB5075ChIP-seq analysis of H-NS in Acinetobacter baumannii AB50752024-07-162024-07-16PRJEB72534