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SRX4742928: piD1 GFP cell
1 ILLUMINA (HiSeq X Ten) run: 16.3M spots, 4.9G bases, 1.9Gb downloads

Design: monkey blastocysts after injection of pESCs were cultured on 8-well IbiTreat -plates (IB-80826; Ibidi GmbH) with in vitro culture media in 5% CO2 incubator. For the first 24 h, the GFP single cell were isolated. Embryos were digested into single cells following treatment with 0.5% Trypsin. Cells were grouped with GFP negative or positive using inverted fluorescence microscope. GFP+ injected cells and GFP- host embryonic cells were collected for gene expression analysis, respectively. To exclude GFP cell marker expression used in PCR may come from recipient embryonic cells, single GFP+ cells were picked up under fluorescence microscopy, respectively. The contaminations of the host embryonic cells were excluded before performing RNA isolation. cDNAs synthesis and amplification were performed with Discover-sc WTA Kit V2 (Vazyme N711, China) according to the instruction manual. The qualities of the cDNAs were evaluated by Bioanalyzer 2100.
Submitted by: Kunming University of Science and Technology
Study: cynomolgus monkey Raw sequence reads
show Abstracthide Abstract
Primed Pluripotent Stem Cells to Generate Chimeric Monkeys .
Sample: monkey blastocysts after injection of pESCs were cultured on 8-well IbiTreat -plates (IB-80826; Ibidi GmbH) with in vitro culture media in 5% CO2 incubator. For the first 24 h, the GFP single cell were isolated.
SAMN10134683 • SRS3824231 • All experiments • All runs
Library:
Name: pESC-GFP3
Instrument: HiSeq X Ten
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Runs: 1 run, 16.3M spots, 4.9G bases, 1.9Gb
Run# of Spots# of BasesSizePublished
SRR790678616,309,3284.9G1.9Gb2019-01-01

ID:
6426308

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