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Repository Table R3 Phosphoproteomics IMAC n1.tab
Version 1.1
File Citation
Haneke, Katharina; Stoecklin, Georg, 2020, "Repository Table R3 Phosphoproteomics IMAC n1.tab", CDK1 couples proliferation with protein synthesis [Repository Tables R1-R4], https://doi.org/10.11588/data/EFHOBZ/JZCMUK, heiDATA, V1, UNF:6:JfKZnmkORxFSPz0dUd0TcQ== [fileUNF]

This file is part of "CDK1 couples proliferation with protein synthesis [Repository Tables R1-R4]".

Dataset Citation
Haneke, Katharina; Stoecklin, Georg, 2020, "CDK1 couples proliferation with protein synthesis [Repository Tables R1-R4]", https://doi.org/10.11588/data/EFHOBZ, heiDATA, V1, UNF:6:+D39RBZQyWVzfn6Sv1nj+w== [fileUNF]
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Data
doi:10.11588/data/EFHOBZ/JZCMUK
UNF:6:JfKZnmkORxFSPz0dUd0TcQ==
157a53ed1a8bf99eae81359b9cc5300c
2020-02-06
453.7 KB
Tab-Delimited
9
2918
HeLa cells were SILAC-labeled and treated with DMSO (light) or Ro3306 (heavy, 10 µM) for 4 h. After lysis and disassembly of polysomes in low magnesium buffer, samples were mixed, and ribosomal fractions obtained by sucrose density centrifugation were subjected to Wessel-Flügge precipitation. Phosphopeptides were enriched using PhosSelect iron affinity gel IMAC beads, fractionated and analyzed by mass spectrometry followed by MaxQuant analysis.
2019-11-21
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