Experiment summary for ENCSR026XFP

doi:10.17989/ENCSR026XFP

Summary

Status
released
Assay
RIP-seq
Target
mub
Biosample summary
Drosophila melanogaster strain Oregon-R S2R+ stably expressing mub treated with 0.35 mM copper(II) sulfate for 24 hours
Biosample Type
cell line
Replication type
isogenic
Description
RIP-seq targeting mub in Drosophila S2R+ cells.
Treatments
0.35 mM copper(II) sulfate (CHEBI:23414) for 24 hours
Nucleic acid type
RNA
Size range
>200
Fragmentation methods
chemical (generic)
Size selection method
AMPure XP bead purification
Strand specificity
unstranded
Controls

Attribution

modENCODE Project
Lab
Brenton Graveley, UConn
Award
U01HG004271 (Susan Celniker, LBNL)
Project
modENCODE
References
Aliases
brenton-graveley:S2R+-CG7437-HA_RIP, modencode:5426
Date submitted
March 31, 2014
Date released
March 31, 2014

Isogenic replicates

Isogenic replicate
Technical replicate
Summary
Biosample
Modifications
Antibody
Library
11Drosophila melanogaster strain Oregon-R S2R+ cell line stably expressing C-terminal HA-tagged mub under MtnA promoter, C-terminal FLAG-tagged mub under MtnA promoter treated with 0.35 mM copper(II) sulfate for 24 hoursENCBS382JGXENCGM463IQTENCAB639FUHENCLB143FQW
21Drosophila melanogaster strain Oregon-R S2R+ cell line stably expressing C-terminal HA-tagged mub under MtnA promoter, C-terminal FLAG-tagged mub under MtnA promoter treated with 0.35 mM copper(II) sulfate for 24 hoursENCBS355XFZENCGM463IQTENCAB639FUHENCLB225NPD