Experiment summary for ENCSR432JLI

doi:10.17989/ENCSR432JLI

Summary

Status
released
Assay
RIP-seq
Biosample summary
Drosophila melanogaster strain Oregon-R S2R+ stably expressing snRNP-U1-70K treated with 0.35 mM copper(II) sulfate for 24 hours
Biosample Type
cell line
Replication type
isogenic
Description
RIP-seq targeting snRNP-U1-70K 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+-CG8749-HA_RIP, modencode:5428
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 FLAG-tagged snRNP-U1-70K under MtnA promoter, C-terminal HA-tagged snRNP-U1-70K under MtnA promoter treated with 0.35 mM copper(II) sulfate for 24 hoursENCBS552ENGENCGM194EHBENCAB639FUHENCLB215ODF
21Drosophila melanogaster strain Oregon-R S2R+ cell line stably expressing C-terminal FLAG-tagged snRNP-U1-70K under MtnA promoter, C-terminal HA-tagged snRNP-U1-70K under MtnA promoter treated with 0.35 mM copper(II) sulfate for 24 hoursENCBS937EMZENCGM194EHBENCAB639FUHENCLB269TZL