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Status |
Public on Oct 31, 2020 |
Title |
RNA sequencing of Hes5.3+ cells from E5 chick embryonic retinas in control and retinoic acid treated conditions. |
Organism |
Gallus gallus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Two E5 (HH26) chick embryonic retinas were dissected from two embryos, electroporated with Hes5.3-GFP reporter plasmid, and incubated in 2.5 μM retinoic acid (RA) in culture medium (DMEM, 10% FBS, 1% Penicillin/Streptomycin) for 8 hours. The corresponding opposite retinas from the same embryos were used as controls and incubated in culture medium with DMSO. Cells were dissociated and GFP+ cells were sorted by FACS. RNA was extracted using TRIzol reagent, according to manufacturer's protocol. RNA samples were quantified by Qubit 4 fluorometer (Thermo Fisher), and RNA quality was assessed by BioAnalyzer (Agilent). RNA sequencing was performed. This protocol was done in triplicate for RA and control conditions.
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Overall design |
Gene expresson by RNA-seq in Hes5.3+ cells from two E5 chick embryonic retinas taken from two different embryos and treated with RA, vs two control retinas from the opposite side of the same embryos, in triplicate.
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Contributor(s) |
Brodier L, Matter J |
Citation missing |
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Submission date |
Mar 05, 2020 |
Last update date |
Oct 31, 2020 |
Contact name |
Laurent Brodier |
E-mail(s) |
laurent.brodier@unige.ch
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Organization name |
University of Geneva
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Department |
Molecular Biology
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Street address |
30 Quai Ernest-Ansermet
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City |
Geneva |
State/province |
Geneva |
ZIP/Postal code |
1211 |
Country |
Switzerland |
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Platforms (1) |
GPL23499 |
Illumina HiSeq 4000 (Gallus gallus) |
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Samples (6)
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Relations |
BioProject |
PRJNA610527 |
SRA |
SRP251687 |