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Status |
Public on Jun 02, 2021 |
Title |
Inflammation drives alternative first exon usage of critical immune genes including Aim2 [RNA-seq] |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Macrophage cells are essential components of the innate immune system and contain toll-like receptors (TLRs) that intiate the immune response when pathogen-associated molecular pattern molecules (PAMPs) are recognized. In this experiment, we stimulate TLR4 in bone marrow-derived macrophage cells with lipopolysaccharide (LPS) for 6 hours to simmulate inflammation and study the resulting differential splicing landscape and gene expression.
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Overall design |
Unstimulated or LPS stimulated Primary Bone Marrow Derived Macrophages (BMDMs) from WT mice were collected and placed in Trizol. RNA was isolated and sequenced using Illumina.
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Contributor(s) |
Carpenter S, Brooks A |
Citation(s) |
34047695 |
Submission date |
Dec 09, 2019 |
Last update date |
Sep 01, 2021 |
Contact name |
Sergio Covarrubias |
E-mail(s) |
secovarr@ucsc.edu
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Phone |
2132710156
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Organization name |
UCSC
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Department |
MCD
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Lab |
Carpenter
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Street address |
Thimann Receiving/Department Carpenter Lab/Biomed 125, 1156 High St., Thimann Labs
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City |
Santa Cruz |
State/province |
CA |
ZIP/Postal code |
95064 |
Country |
USA |
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Platforms (1) |
GPL21493 |
Illumina HiSeq 3000 (Mus musculus) |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE141754 |
Inflammation drives alternative first exon usage of critical immune genes including Aim2 |
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Relations |
BioProject |
PRJNA594369 |
SRA |
SRP235279 |