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| Hauptseite > Publikationsdatenbank > Dataset containing physiological amounts of spike-in proteins into murine C2C12 background as a ground truth quantitative LC-MS/MS reference > print |
| Hauptseite > Publikationsdatenbank > Dataset containing physiological amounts of spike-in proteins into murine C2C12 background as a ground truth quantitative LC-MS/MS reference > print |
| 001 | 910685 | ||
| 005 | 20230228121558.0 | ||
| 024 | 7 | _ | |a 10.1016/j.dib.2022.108435 |2 doi |
| 024 | 7 | _ | |a 2128/33804 |2 Handle |
| 024 | 7 | _ | |a 35845101 |2 pmid |
| 024 | 7 | _ | |a WOS:000828066500003 |2 WOS |
| 037 | _ | _ | |a FZJ-2022-04057 |
| 082 | _ | _ | |a 570 |
| 100 | 1 | _ | |a Uszkoreit, Julian |0 P:(DE-Juel1)192371 |b 0 |e Corresponding author |u fzj |
| 245 | _ | _ | |a Dataset containing physiological amounts of spike-in proteins into murine C2C12 background as a ground truth quantitative LC-MS/MS reference |
| 260 | _ | _ | |a Amsterdam [u.a.] |c 2022 |b Elsevier |
| 336 | 7 | _ | |a article |2 DRIVER |
| 336 | 7 | _ | |a Output Types/Journal article |2 DataCite |
| 336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1675058409_21129 |2 PUB:(DE-HGF) |
| 336 | 7 | _ | |a ARTICLE |2 BibTeX |
| 336 | 7 | _ | |a JOURNAL_ARTICLE |2 ORCID |
| 336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
| 520 | _ | _ | |a In this article, we present a data dependent acquisition (DDA) dataset which was generated as a reference and ground truth quantitative dataset. While initially used to compare samples measured with DDA and data independent acquisition (DIA) (Barkovits et al., 2020), the presented dataset holds potential value as a benchmark reference for any workflows working on DDA data. The entire dataset consists of 15 LC-MS/MS measurements composed of five distinct spike-in-states, each with three replicates. To generate the data set, a C2C12 (immortalized mouse myoblast) cell lysate was used as a complex background for five different states which were simulated by spiking 13 defined proteins at different concentrations. For this purpose, the cell lysate was used in a constant amount of 20 µg for all samples and different amounts of the 13 selected proteins ranging from 0.1 to 10 pmol were added, reflecting physiological amounts of proteins. Afterwards, all samples were tryptically digested using the same method. From each sample 200 ng tryptic peptides were measured in triplicates on a Q Exactive HF (Thermo Fisher Scientific). The mass range for MS1 was set to 350–1400 m/z with a resolution of 60,000 at 200 m/z. HCD fragmentation of the Top10 abundant precursor ions was performed at 27% NCE. The fragment analysis (MS2) was performed with a resolution of 30,000 at 200 m/z. |
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| 588 | _ | _ | |a Dataset connected to CrossRef, Journals: juser.fz-juelich.de |
| 700 | 1 | _ | |a Barkovits, Katalin |0 P:(DE-HGF)0 |b 1 |
| 700 | 1 | _ | |a Pacharra, Sandra |0 P:(DE-HGF)0 |b 2 |
| 700 | 1 | _ | |a Pfeiffer, Kathy |0 P:(DE-HGF)0 |b 3 |
| 700 | 1 | _ | |a Steinbach, Simone |0 P:(DE-HGF)0 |b 4 |
| 700 | 1 | _ | |a Marcus, Katrin |0 P:(DE-HGF)0 |b 5 |
| 700 | 1 | _ | |a Eisenacher, Martin |0 0000-0003-2687-7444 |b 6 |
| 773 | _ | _ | |a 10.1016/j.dib.2022.108435 |g Vol. 43, p. 108435 - |0 PERI:(DE-600)2786545-9 |p 108435 - |t Data in Brief |v 43 |y 2022 |x 2352-3409 |
| 856 | 4 | _ | |u https://juser.fz-juelich.de/record/910685/files/1-s2.0-S2352340922006321-main.pdf |y OpenAccess |
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