Experiment summary for ENCSR291KUB

doi:10.17989/ENCSR291KUB

Summary

Status
released
Assay
ChIP-seq (TF ChIP-seq)
Target
Rel
Biosample summary
Drosophila melanogaster strain Rel-GFP whole organism wandering third instar larva genetically modified (insertion) using site-specific recombination targeting D. melanogaster Rel
Biosample Type
whole organisms
Replication type
isogenic
Description
ChIP-seq on transgenic flies expressing Rel-eGFP fusion proteins. The IP was performed using an anti-GFP antibody.
Nucleic acid type
DNA
Size range
200-800
Fragmentation methods
sonication (Bioruptor generic)
Size selection method
SPRI beads
Controls

Attribution

modERN project
Lab
Kevin White, UChicago
Award
U41HG007355 (Robert Waterston, UW)
Project
modERN
External resources
Aliases
kevin-white:Rel-GFP
Date submitted
July 24, 2015
Date released
July 6, 2016
Submitter comment
ENCFF707KFY, ENCFF584KZL were revoked because a software bug accidentally truncated the file content. The submitters have provided replacement files. This experiment was conducted with C-terminally tagged Rel. The majority of full-length Rel protein is localized to the cytoplasm prior to cleavage, when the N-terminal portion can translocate into the nucleus. We plan on repeating this experiment with an N-terminal GFP tag.

Encyclopedia Integration

Isogenic replicates

Isogenic replicate
Technical replicate
Summary
Biosample
Modifications
Antibody
Library
21Drosophila melanogaster strain Rel-GFP mixed sex wandering third instar larva whole organism genetically modified (insertion) using site-specific recombination targeting D. melanogaster RelENCBS079KXGENCGM696ISOENCAB728YTOENCLB146SRJ
31Drosophila melanogaster strain Rel-GFP mixed sex wandering third instar larva whole organism genetically modified (insertion) using site-specific recombination targeting D. melanogaster RelENCBS853AJHENCGM696ISOENCAB728YTOENCLB916EEP