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Status |
Public on Sep 28, 2022 |
Title |
mRNA-sequencing of ILC1 cells |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Purpose: To understanding the effects of RORa deficiency on ILC1 cells, we conducted bulk mRNA-seqencing Method: Firstly, we purified liver ILC1 cells (CD45.2+CD3-CD19-NKp46+NK1.1+CD49a+CD49b-) via Fluorescence Activated Cell Sorting, then frozen in -80 °C ultra-low temperature refrigerator, followed by High-throughput sequencing, in three replicates for WT (Rorafl/fl) mice and one replicate for cKO (Ncr1Cre-Rorafl/fl) , using Illumina Hiseq 1500 platform.
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Overall design |
Find the DEGs in cKO ILC1 cells
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Contributor(s) |
Song J, Song H, Sun R, Tian Z, Peng H |
Citation(s) |
34510508 |
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Submission date |
Oct 20, 2021 |
Last update date |
Sep 28, 2022 |
Contact name |
Zhigang Tian |
E-mail(s) |
tzg@ustc.edu.cn
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Phone |
+8615665425083
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Organization name |
Univerity of Science and Technology of China
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Street address |
Huangshan Road,number 443
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City |
Hefei |
State/province |
Anhui |
ZIP/Postal code |
230000 |
Country |
China |
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Platforms (1) |
GPL18480 |
Illumina HiSeq 1500 (Mus musculus) |
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Samples (4)
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Relations |
BioProject |
PRJNA772937 |
SRA |
SRP342256 |