PXD014235

PXD014235 is an original dataset announced via ProteomeXchange.

Title	IgG purification- MS analysis - MS analysis was undertaken on human IgG purified using different approaches to assess purifity and potential alterations within the IgG N-linked glycans
Description	MS analysis was undertaken on human IgG purified using different approaches to assess purifity and potential alterations within the IgG N-linked glycans
HostingRepository	PRIDE
AnnounceDate	2021-03-04
AnnouncementXML	Submission_2021-03-04_12:11:54.526.xml
DigitalObjectIdentifier
ReviewLevel	Peer-reviewed dataset
DatasetOrigin	Original dataset
RepositorySupport	Unsupported dataset by repository
PrimarySubmitter	Nichollas Scott
SpeciesList	scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationList	complex glycosylation
Instrument	Orbitrap Fusion Lumos; LTQ Orbitrap Elite

Revision	Datetime	Status	ChangeLog Entry
0	2019-06-12 08:43:26	ID requested
⏵ 1	2021-03-04 12:11:54	announced

Dataset with its publication pending

submitter keyword: Human, IgG, Protein A purification, Melon gel

Amy Chung
contact affiliation	SENIOR RESEARCH FELLOW(NHMRC TRAINING FELLOWSHIP), Chung Lab, Department of Microbiology and Immunology / Peter Doherty Institute, University of Melbourne Melbourne, Victoria, Australia
contact email	awchung@unimelb.edu.au
lab head
Nichollas Scott
contact affiliation	University of Melbourne
contact email	nichollas.scott@unimelb.edu.au
dataset submitter

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/2019/11/PXD014235

PRIDE project URI

• PRIDE
  1. PXD014235
     1. Label: PRIDE project
     2. Name: IgG purification- MS analysis - MS analysis was undertaken on human IgG purified using different approaches to assess purifity and potential alterations within the IgG N-linked glycans