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SRX16252989: GSM6340068: UB cells,cKO,E16.5,biol rep 2 [B_2]; Mus musculus; RNA-Seq
1 ILLUMINA (HiSeq X Ten) run: 22.8M spots, 6.7G bases, 2Gb downloads

External Id: GSM6340068_r1
Submitted by: Shanghai Jiaotong University School of Medicine
Study: ASH2L controls ureteric bud morphogenesis via regulation of RET/GFRA1 signaling activity [RNA-seq]
show Abstracthide Abstract
To elucidate the role of H3K4 methylation in metanephros development, we selectively inactivated ASH2L, core subunit of the COMPASS complex in mice UB lineage. We then performed gene expression profiling analysis using data obtained from RNA-seq of 3 different FACS-sorted UB lineage cells at E16.5 of the control and cKO mouse embryos. Overall design: Comparative gene expression profiling analysis of RNA-seq data for FACS-sorted UB lineage cells at E16.5 of control and Ash2l cKO mouse embryos.
Sample: UB cells,cKO,E16.5,biol rep 2 [B_2]
SAMN29765766 • SRS13893028 • All experiments • All runs
Organism: Mus musculus
Library:
Name: GSM6340068
Instrument: HiSeq X Ten
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: RNA was harvested using mirVana miRNA Isolation Kit (Ambion). RNA purity and quantification were evaluated using the NanoDrop 2000 spectrophotometer (Thermo Scientific, USA). RNA integrity was assessed using the Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA). Then the libraries were constructed using TruSeq Stranded mRNA LT Sample Prep Kit (Illumina, San Diego, CA, USA) according to the manufacturer's instructions. The transcriptome sequencing and analysis were conducted by OE Biotech Co., Ltd. (Shanghai, China).
Runs: 1 run, 22.8M spots, 6.7G bases, 2Gb
Run# of Spots# of BasesSizePublished
SRR2021882322,785,5116.7G2Gb2023-01-19

ID:
22962730

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