Notice: Temporary Suspension of New Experiment Creation
We have temporarily disabled the creation of new experiments as we are continuously running out of space. This issue has been impacting both uploads and downloads from FlowRepository. By taking this step, we aim to make downloads of existing data more reliable.
We apologize for the inconvenience and appreciate your understanding as we work on upgrading our hardware and improving the overall solution.
Thank you for your patience.

Download-button_s

Experiment Overview

Repository ID: FR-FCM-Z333 Experiment name: Inhibition of uracil removal by ATA in MCF7 cells MIFlowCyt score: 46.61%
Primary researcher: Daniel Laverty PI/manager: Zachary Nagel Uploaded by: Daniel Laverty
Experiment dates: 2020-08-29 - 2020-09-13 Dataset uploaded: Oct 2020 Last updated: Apr 2024
Keywords: [DNA Repair] Manuscripts: [29122935]
Organizations: Harvard T.H. Chan School of Public Health, Boston, MA (United States)
Purpose: Testing the inhibition of uracil removal from DNA by the inhibitor ATA.
Conclusion: ATA inhibits the removal of uracil from a plasmid based assay in MCF7 cells
Comments: MCF7 cells were seeded into plates and treated with DMSO or with a putative uracil dna glycosylase inhibitor (ATA, sometimes referred to as ATA mix). Following treatment, cells were transfected with a plasmid-based reporter that measures uracil removal. The samples labelled "Undamaged" were transfected with plasmids encoding BFP and GFP. The samples labeled "Damaged" were transfected with a plasmid encoding GFP and a uracil-containing plasmid encoding BFP. If uracil is present in the plasmid, wild type BFP transcripts are produced. If uracil is removed. non-fluorescent transcripts are produced. Hence, increased BFP fluorescence in the samples labeled "Damaged" means decreased removal of uracil from DNA.
Funding: Not disclosed
Quality control: Daily performance tests on the flow cytometer using the manufacturer's performance tracking beads.
Download FCS Files or login and see the dataset in your inbox for further annotation details.