PXD023563 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Targeted analysis of alternative protein isoforms in AC16 cells |
Description | AC16 cells (Human Cardiomyocyte Cell Line) were digested by trypsin and analyzed by parallel reaction monitoring. |
HostingRepository | PRIDE |
AnnounceDate | 2022-05-19 |
AnnouncementXML | Submission_2022-05-19_13:05:13.883.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Maggie Pui Yu Lam |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | No PTMs are included in the dataset |
Instrument | Q Exactive HF |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2021-01-13 00:19:33 | ID requested | |
⏵ 1 | 2022-05-19 13:05:14 | announced | |
Publication List
Han Y, Wood SD, Wright JM, Dostal V, Lau E, Lam MPY, Computation-assisted targeted proteomics of alternative splicing protein isoforms in the human heart. J Mol Cell Cardiol, 154():92-96(2021) [pubmed] |
Keyword List
submitter keyword: AC16, PRM |
Contact List
Maggie Pui Yu Lam, PhD |
contact affiliation | University of Colorado, Anschutz Medical Campus |
contact email | maggie.lam@cuanschutz.edu |
lab head | |
Maggie Pui Yu Lam |
contact affiliation | UC Denver, Anschutz Medical Campus |
contact email | maggie.lam@ucdenver.edu |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2022/05/PXD023563 |
PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD023563
- Label: PRIDE project
- Name: Targeted analysis of alternative protein isoforms in AC16 cells