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Status |
Public on Sep 13, 2012 |
Title |
ChIPseq analysis of IRF4 and BATF in immune cells |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Purpose: The purpose of this study is to find the binding partner of IRF4 in the context of Th17- cell differentiation. To this end, we have used ChIPseq analysis followed by de novo motif search around genome-wide binding sites to identify BATF as the binding partner for IRF4 in the context of not only Th17 cells but other immune cell types as well.
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Overall design |
Naïve T-cells isolated from the spleen of C57BL/6J mice are cultured under Th17, Th2 or Th0 polarizing conditions for 42 hrs and subject to ChIP using IRF4 and/or BATF antibodies followed by high-throughput sequencing. Bone marrow derived dendritic cells (BMDCs) were stimulated with LPS for 6hrs and similrly subjected to ChIPseq analysis with IRF4.
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Contributor(s) |
Agrawal S, Zeng W, Lugt B |
Citation(s) |
22983707 |
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Submission date |
Sep 10, 2012 |
Last update date |
May 15, 2019 |
Contact name |
Smita Agrawal |
Organization name |
Genentech Inc.
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Department |
Immunology
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Street address |
1 DNA Way
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City |
South San Francisco |
State/province |
CA |
ZIP/Postal code |
94080 |
Country |
USA |
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Platforms (2) |
GPL11002 |
Illumina Genome Analyzer IIx (Mus musculus) |
GPL13112 |
Illumina HiSeq 2000 (Mus musculus) |
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Samples (9)
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This SubSeries is part of SuperSeries: |
GSE40483 |
A genomic regulatory element that directs assembly and function of immunespecific AP-1-IRF complexes |
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Relations |
BioProject |
PRJNA174767 |
SRA |
SRP015676 |