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SRX4742915: piD1 GFP cell
1 ILLUMINA (HiSeq X Ten) run: 15M spots, 4.5G bases, 1.6Gb downloads

Design: monkey blastocysts after injection of dESCs 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 dESCs 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.
SAMN10134700 • SRS3824218 • All experiments • All runs
Library:
Name: dESC-GFP2
Instrument: HiSeq X Ten
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Runs: 1 run, 15M spots, 4.5G bases, 1.6Gb
Run# of Spots# of BasesSizePublished
SRR790679914,967,4994.5G1.6Gb2019-01-01

ID:
6426295

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