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Status |
Public on Mar 01, 2018 |
Title |
Gene expression in Sox9 progenitors in the developing mouse lung |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing Other
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Summary |
This submission consists of two experiments utilizing translating ribosome affinity purification-sequencing (TRAP-seq). The first uses TRAP-seq to isolate transcripts from Sox9 positive progenitors at E14 and an E17 lung and compares it to non-immunoprecipitated whole lung homogenate control. The second compares TRAP-seq isolated transcripts from Sox9-wild type progenitors versus mutant progenitors. Recombination was induced at E13 and cells were isolated at E16.
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Overall design |
Sox9-TRAP at E14 vs supernatant; Sox9-TRAP at E17 vs whole lung homogenate; duplicated Sox9-mutant versus Sox9-wild-type
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Contributor(s) |
Chen J, Ostrin E |
Citation(s) |
29440304 |
NIH grant(s) |
Grant ID |
Grant title |
Affiliation |
Name |
R01 HL130129 |
Role of AT1 cells in perinatal lung maturation |
The University of Texas MD Anderson Cancer Center |
JICHAO CHEN |
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Submission date |
Jul 18, 2017 |
Last update date |
Jul 25, 2021 |
Contact name |
Edwin Justin Ostrin |
E-mail(s) |
ejostrin@mdanderson.org
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Organization name |
MD Anderson Cancer Center
|
Department |
Pulmonary Medicine
|
Street address |
1515 Holcombe Blvd, Unit 1465
|
City |
Houston |
State/province |
Texas |
ZIP/Postal code |
77030 |
Country |
USA |
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Platforms (1) |
GPL21103 |
Illumina HiSeq 4000 (Mus musculus) |
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Samples (8)
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Relations |
BioProject |
PRJNA394882 |
SRA |
SRP112742 |