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SRX7007335: GSM4125657: microglia_M689; Mus musculus; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 26.2M spots, 3.9G bases, 1.5Gb downloads

Submitted by: NCBI (GEO)
Study: Analysis of NSL knockout brains
show Abstracthide Abstract
In the current study, we analyse the function of MOF-NSL complex in neural cells. We find that the NSL complex regulates metabolic networks in the brain. Overall design: Knockout of NSL complex members Mof, Kansl2 and Kansl3 was induced using the Nestin Cre. Neural cells, endothelial cells, pericytes and microglia were isolated by FACS. Gene expression analysed by RNA seq. and chromatin landscape via ChIP seq.
Sample: microglia_M689
SAMN13041614 • SRS5528505 • All experiments • All runs
Organism: Mus musculus
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: RNA from cultured pericytes, whole E14.5 brains and from neural cells was isolated using the Qiagen mini kit (#74104), while RNA from pericytes, endothelial cells and microglia was extracted using the Qiagen miRNeasy Micro kit (#1071023). Libraries for RNA-seq of cultured pericytes, whole E14.5 brains and the neural population were prepared using the Illumina TruSeq library preparation kit. For pericytes, endothelial cells and microglia, cDNA was prepared from isolated RNA using the SMART-Seq v4 Ultra Low Input RNA Kit for Sequencing (Clontech 634891). Libraries were prepared using the Nextera XT DNA library preparation kit (Illumina FC-131-1096) and sequenced on the HiSeq Hiseq 3000 or NextSeq 500. ChIP and library preparation for IP DNA was undertaken using the RELACS protocol (Arrigoni et al. 2018 Communications Biology)
Experiment attributes:
GEO Accession: GSM4125657
Links:
Runs: 1 run, 26.2M spots, 3.9G bases, 1.5Gb
Run# of Spots# of BasesSizePublished
SRR1029445426,197,0003.9G1.5Gb2020-04-01

ID:
9210430

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