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SRX15038779: GSM6071122: 12RFP, d10; Homo sapiens; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 33.7M spots, 10.1G bases, 3.5Gb downloads

External Id: GSM6071122_r1
Submitted by: Environmental Epigenetics, Bioscience, KAUST- King Abdullah university of science and technology
Study: LINE-1 retrotransposons are reduced in bone of osteoporotic patients, correlate positively to BMD, and stimulate bone anabolism in transfected mesenchymal stem cells
show Abstracthide Abstract
To investigate the role of LINE-1 in bone regeneration, we delivered synthetic L1 RNA to mesenchymal stem cells (MSC), from osteoporotic patients, induced to osteogenic differentiation. Overall design: First, mesenchymal stem cells (MSC) from femur of 4 osteoporotic patients (HUK9, HUK12, HUK16, HUK19) were isolated. MSC were then induced to osteogenic differentiation and transfected after 5 days with RFP mRNA (negative control) or L1 RNA. Samples were collected at day 6 (24h post-transfection) and day 10 (5 days post-transfection). Comparative gene expression profiling analysis of RNA-seq data for RFP mRNA and L1 RNA transfected cells was performed.
Sample: 12RFP, d10
SAMN27926692 • SRS12785541 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: GSM6071122
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Cells were harvested and resuspended in 1ml of QIAzol Lysis reagent (Qiagen, Cat. No.79306). Total RNA was then purified with RNeasy Plus Mini kit (Qiagen, cat. No. 74134) with minimal modifications to manufacturer's instructions. DNase treatment (RNase free DNase set, Qiagen, Cat. No. 79254) was performed to remove any residual DNA. RNA quality and concentration were checked using a NanodropTM 2000 spectrophotometer (ThermoFisher). Total RNA-seq library was prepared with CORALL Total RNA library prep with RiboCop rRNA for Human/Mouse/Rat depletion kit (Lexogen GmbH, Vienna, Austria) following manufacturer's instructions (library type: fr-secondstrand) by IGA Technology service (Italy). Final libraries were checked with both Qubit 2.0 Fluorometer (Invitrogen, Carlsbad, CA) and Agilent Bioanalyzer DNA assay or Caliper (PerkinElmer, Waltham, MA).
Runs: 1 run, 33.7M spots, 10.1G bases, 3.5Gb
Run# of Spots# of BasesSizePublished
SRR1896166933,728,95810.1G3.5Gb2024-09-13

ID:
21511115

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