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SRX5192755: GSM3536166: MS275-rep3: E13.5_NSPCs_MS275-3_RNA-seq; Mus musculus; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 22.1M spots, 6.6G bases, 2Gb downloads

Submitted by: NCBI (GEO)
Study: ChIP-seq and RNA-seq analysis of histone Kcr in the embryonic forebrain and neural stem/progenitor cells.
show Abstracthide Abstract
To gain a deeper insight into how histone lysine crotonylation regulates embryonic neural stem/progenitor cells (NSPCs) proliferation and differentiation, ChIP-seq and RNA-seq were performed to analyze the genome-wide changes of histone Kcr and transcriptiome changes stimulated with crotonate and MS-275 in E13.5 NSPCs. Overall design: Total RNA was extracted from E13.5 NSPCs before and after crotonate and MS-275 stimulation and generated by deep sequencing, in four biological replicates, using Illumina novaseq 6000. ChIP was excuted using pan-Kcr and Pan-Kac antibody with E13.5 NSPCs before and after crotonate and MS-275 stimulation.
Sample: Transcriptome_E13.5_NSPCs_MS-275-rep3_RNA-seq
SAMN10678419 • SRS4198790 • All experiments • All runs
Organism: Mus musculus
Library:
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Lysates were clarified from sonicated nuclei and histone-DNA complexes were isolated with antibody. RNA was harvested using Trizol reagent. NEBNext® Ultra™ RNA library prep kit for Illumina® (NEB) was used with 2 ug of total RNA for the construction of sequencing libraries. ChIP's DNA was subjected to end-repair and then was 3'adenylated. Adaptors were ligated to the ends of these 3'adenylated fragments. Next, polymerase chain reaction amplification was to amplify those fragments with adaptors from previous step. RNA libraries were prepared for sequencing using standard Illumina protocols.
Experiment attributes:
GEO Accession: GSM3536166
Links:
Runs: 1 run, 22.1M spots, 6.6G bases, 2Gb
Run# of Spots# of BasesSizePublished
SRR838281022,104,6656.6G2Gb2019-05-02

ID:
7023842

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