IL34
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
TNR
Gene Ontology Biological Process
- associative learning [IMP]
- extracellular matrix organization [IMP]
- locomotory exploration behavior [IMP]
- long-term synaptic potentiation [IMP]
- negative regulation of axon extension [IDA]
- negative regulation of axon extension involved in regeneration [IMP]
- negative regulation of cell adhesion [ISO]
- negative regulation of cell-cell adhesion [IDA, IMP]
- negative regulation of neuron projection development [IDA]
- negative regulation of synaptic transmission [IMP]
- neuromuscular process controlling balance [IMP]
- neuron cell-cell adhesion [IMP]
- positive regulation of synaptic transmission, glutamatergic [IMP]
- positive regulation of transmission of nerve impulse [IMP]
- regulation of synaptic transmission [IMP]
- synapse organization [IMP]
- telencephalon cell migration [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Affinity Capture-MS
An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner is identified by mass spectrometric methods.
Publication
Receptor-type protein-tyrosine phosphatase ζ is a functional receptor for interleukin-34.
Interleukin-34 (IL-34) is highly expressed in brain. IL-34 signaling via its cognate receptor, colony-stimulating factor-1 receptor (CSF-1R), is required for the development of microglia. However, the differential expression of IL-34 and the CSF-1R in brain suggests that IL-34 may signal via an alternate receptor. By IL-34 affinity chromatography of solubilized mouse brain membrane followed by mass spectrometric analysis, we identified ... [more]
Throughput
- Low Throughput
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
IL34 TNR | Affinity Capture-Western Affinity Capture-Western An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins. | Low | - | BioGRID | - |
Curated By
- BioGRID