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ProteomicsCo-IP (AP-MS) of Connexin-43 - Gap junction protein Connexin-43 is a direct transcriptional regulator of N-cadherin in vivo
Co-IP Experiment Bait: Cx43-Flag Cell line: Hela Related Publication: Gap Junction protein Connexin-43 is a direct transcriptional regulator of N-cadherin in vivo, Maria Kotini, Elias Barriga, Jonathan Leslie, Marc Gentzel, Verena Rauschenberger, Alexandra Schambony, and Roberto Mayor
ORGANISM(S): Homo sapiens (Human) 
2018-10-16 | PXD010870 | Pride
Ap-ms Hela Co-ip 
ProteomicsCo-IP/MS for determining interacting partners of TSG-6 in human pHSCs
Interacting partners of TSG-6 were analyzed by coimmunoprecipitation (co-IP) coupled with liquid chromatography tandem mass spectrometry (LC–MS/MS)
ORGANISM(S): Homo sapiens (Human) 
2024-06-16 | PXD047449 | Pride
Human Tsg-6 Primary hepatic stellate cells Co-ip/ms 
ProteomicsUPLC-MS/MS of YAP co-IP during activating and inactivating plating conditions
To identify YAP binding partners potentially involved in mechanotransduction, we performed a YAP co-IP/MS experiment using sparsely or densely plated MCF10A cells.
ORGANISM(S): Homo sapiens (Human) 
2019-11-21 | PXD007287 | Pride
Dense Yap Co-ip Sparse Mammary epithelial cells Mcf10a 
ProteomicsLYSET/TMEM251 SILAC Co-IP from MIA PaCA-2
Endogenous LYSET/TMEM251 was isolated via Co-IP from MIA PaCa-2 cells. LYSET KO cells were used as controls. Cells were grown in SILAC medium for 3 passages
ORGANISM(S): Homo sapiens (Human) 
2022-09-29 | PXD035821 | Pride
Silac co-ip Human Lyset Tmem251 
ProteomicsAdult mouse choroid plexus OTX2 Co-IP
To analyze OTX2 function in adult choroid plexus, we performed several OTX2 co-immunoprecipitation (co-IP) experiments with mass spectrometry analysis to identify potential protein partners. We previously discovered that OTX2 protein also accumulates non-cell autonomously in subventricular zone (SVZ...
ORGANISM(S): Mus musculus (Mouse) 
2021-08-23 | PXD021244 | Pride
Homeoprotein Mouse Otx2 Choroid plexus 
ProteomicsMassProteomic Analysis of MIRO2 Interacting Proteins by Co-IP and Mass Spectrometry
This project investigates the interactome of MIRO2 using co-immunoprecipitation (Co-IP) followed by mass spectrometry analysis. Control and MIRO2-FLAG overexpressing cells were subjected to Co-IP to identify proteins that interact with MIRO2 and potentially facilitate mitochondrial-derived vesicle (...
ORGANISM(S): Homo sapiens (Human) 
2026-06-03 | PXD078488 | Pride
Human Miro2-flag B-fission 
ProteomicsCo-IP of v-ATPase subcomplexes from MEFs under amino acid starvation and restimulation
v-ATPase Vo and V1 domains were isolated via Co-IP from MEFs expressing HA-Atp6V1B2 and FLAG-Atp6VoaA3 using HA- and FLAG-tag antibodies. Treatment groups were full medium (control), amino acid starvation (60 min) and restimulation (30 min). Cells were grown in SILAC medium for 3 passages.
ORGANISM(S): Mus musculus (Mouse) 
2022-08-20 | PXD030174 | Pride
Mefs Co-ip Silac Vatpase Amino acid starvation 
ProteomicsCo-immunoprecipitation followed by mass spectrometry (Co-IP/MS) data of HNRNPF.
The interacting proteins of HNRNPF were identified in mouse embryonic stem cells by co-immunoprecipitation followed by mass spectrometry (Co-IP/MS).
ORGANISM(S): Mus musculus (Mouse) 
2025-06-30 | PXD065613 | Pride
Mesc Hnrnpf 
ProteomicsAnnexin A2 facilitates Japanese encephalitis virus replication by regulating endocytosis and intracellular transport in PK15 cells (Co-IP proteomics dataset)
All raw files correspond to porcine kidney epithelial cell (PK15) samples, including two groups: one group named IP-SA14 was the cellular protein from PK15 cell infected with JEV. The other group named IP-kong was control group from normally cultured PK15 cells. all raw spectral data are integrated ...
ORGANISM(S): Sus scrofa domesticus (domestic pig) 
2026-09-14 | PXD081082 | Pride
Envelope proteins of jev Immunoprecipitation Pk15 cell Lc-ms/ms 
ProteomicsTMEM160 Promotes Tumor Growth in Lung Adenocarcinoma and Cervical Adenocarcinoma Cell Lines
This dataset corresponds to the proteomic characterization of the TMEM160 interactome in A549 cells using co-immunoprecipitation (Co-IP) followed by data-independent acquisition mass spectrometry (DIA-MS). TMEM160 was immunoprecipitated using an anti-TMEM160 antibody, and interacting proteins were i...
ORGANISM(S): Homo sapiens (Human) 
2025-12-01 | PXD071042 | Pride
C-hpp  tmem160  non-small cell lung cancer  cervical cancer  tumor growth  nuclear localization dia-nn  dia proteomics  co-ip proteomics  a549 cells 
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