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Status |
Public on May 28, 2020 |
Title |
UPF1 regulatory loop variant RNA-Seq and RIP-Seq |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing Other
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Summary |
HEK-293 Trex cells containing stable tetracycline-inducible transgenes driving overexpression of CLIP-tagged UPF1 isoforms 1 and 2 or GFP were used for total RNA-seq. In addition, CLIP-UPF1 isoforms were affinity purified, and bound RNA was subjected to high-throughput sequencing.
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Overall design |
Paired-end high-throughput RNA sequencing of Total RNA from cells expressing CLIP-tagged UPF1 isoform 1, UPF1 isoform 2, or GFP and RNA associated with affinity-purified CLIP UPF1 isoforms 1 and 2.
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Contributor(s) |
Fritz SE, Hogg JR |
Citation missing |
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Submission date |
Jul 09, 2019 |
Last update date |
May 28, 2020 |
Contact name |
J. Robert Hogg |
E-mail(s) |
j.hogg@nih.gov
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Organization name |
National Heart, Lung, and Blood Institute
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Department |
Biochemistry and Biophysics Center
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Street address |
50 South Drive, Room 2341
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City |
Bethesda |
State/province |
MD |
ZIP/Postal code |
20892 |
Country |
USA |
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Platforms (1) |
GPL21290 |
Illumina HiSeq 3000 (Homo sapiens) |
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Samples (15)
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Relations |
BioProject |
PRJNA553576 |
SRA |
SRP213944 |