Guo Huiling H - OmicsDI

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Proteomics (3)

Organisms

Homo sapiens (2)
Acanthamoeba genotype T4 (1)
Rhodobacter capsulatus (1)
Mycoplasma suis KI3806 (1)
Vicia faba (1)
Aspergillus (1)
Cryptococcus deuterogattii R265 (1)
Cryptococcus deneoformans JEC21 (1)
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Rhodnius prolixus (1)
Cellulophaga lytica (1)
Klebsiella pneumoniae subsp. rhinoscleromatis ATCC 13884 (1)
Trichopria drosophilae (1)
Hepatitis B virus subtype ayw (1)
Francisella tularensis subsp. holarctica LVS (1)
Camponotus floridanus (1)
Plasmodium falciparum 58.1 (1)
Oryzias latipes (1)
Oryza longistaminata (1)
Solenopsis invicta (1)
Japanese encephalitis virus (1)
West Nile virus (1)
Culex pipiens pipiens (1)
Camponotus fellah (1)
Mycoplasmoides pneumoniae 19294 (1)
Xenopsylla cheopis (1)
NEWT:1313166 (1)
Hydra vulgaris (1)
Fusobacterium nucleatum subsp. nucleatum ATCC 25586 (1)
Angiostrongylus (1)

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iProX (2)
pride (1)

Tissue

Cell culture (1)

Technology Type

Bottom-up proteomics (1)
Mass Spectrometry (1)

Publication Date

2023 (1)
2025 (1)

Lab affiliation

Children's Hospital of Fudan University, National Children's Medical Center, and Shanghai Key Laboratory of Medical Epigenetics, International Co-laboratory of Medical Epigenetics and Metabolism, Ministry of Science and Technology, Institutes of Biomedical Sciences, Fudan University, Shanghai, 200032, China (1)

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Proteomic Analysis of USP17LA-Interacting Proteins in 293T Cells

To explore the interaction network of USP17LA, we overexpressed it in HEK293T cells and performed IP-MS to identify associated proteins and potential targets.

ORGANISM(S): Homo sapiens (Human)

2025-11-17 | PXD065847 | Pride

Mass spectrometry analysis of Flag-H9N2-NS2 interacting proteins

ORGANISM(S): Homo Sapiens

PXD056322 |

Low glucose metabolite 3-phosphoglycerate switches PHGDH from serine synthesis to p53 activation to control cell fate

This project identified the interacting proteins of p53 under glucose starvation in HEK293 cells.