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PXD039136 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleHuman,Embryonic Kidney Cells(293T-Vector/Flag-△50),LC-MSMS
DescriptionHutchinson-Gilford progeria syndrome (HGPS) is a premature aging disease caused by progerin accumulation. However, the mechanism of how progerin causes cell defects is unclear in HGPS cells. To further investigate the possible mechanism, we used Flag-tagged progerin as bait in mass spectrometry to survey the possible regulatory factors.
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationListiodoacetamide derivatized residue
InstrumentQ Exactive
Dataset History
RevisionDatetimeStatusChangeLog Entry
02023-01-02 01:22:55ID requested
12023-01-30 02:34:21announced
Publication List
Dataset with its publication pending
Keyword List
submitter keyword: Human, LC-MSMS,progerin, binding protein,293T
Contact List
contact affiliationThe Institute of Genetics and Cytology, Northeast Normal University, Changchun, China
contact emailluj809@nenu.edu.cn
lab head
contact affiliationNortheast Normal University
contact emailzhangn783@nenu.edu.cn
dataset submitter
Full Dataset Link List
Dataset FTP location
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PRIDE project URI
Repository Record List
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