Tnfrsf23

Tnfrsf23 is a member of the tumor necrosis factor superfamily of proteins. Tnfrsf23 has been shown to bind to the ligand TRAIL (tumor necrosis factor-related apoptosis-inducing ligand), but to have no signaling capacity. Tnfrsf23 shows elevated expression in mice with diet-induced fatty liver disease. Tnfrsf23 and other family members are present in a gene cluster on chromosome 7.
Full Name
Tumor Necrosis Factor Receptor Superfamily, Member 23
Function
Receptor for the cytotoxic ligand TRAIL. Lacks a cytoplasmic death domain and hence is not capable of inducing apoptosis. May protect cells against TRAIL mediated apoptosis through ligand competition. Cannot induce the NF-kappa-B pathway.
Biological Process
Biological Process activation-induced cell death of T cells Source:GO_Central1 Publication
Biological Process extrinsic apoptotic signaling pathway in absence of ligand Source:GO_Central1 Publication
Biological Process motor neuron apoptotic process Source:GO_Central1 Publication
Biological Process necroptotic signaling pathway Source:GO_Central1 Publication
Biological Process negative regulation of apoptotic process Source:GO_Central1 Publication
Biological Process negative regulation of extrinsic apoptotic signaling pathway via death domain receptors Source:MGI1 Publication
Biological Process positive regulation of cysteine-type endopeptidase activity involved in apoptotic signaling pathway Source:GO_Central1 Publication
Biological Process regulation of stress-activated MAPK cascade Source:GO_Central1 Publication
Cellular Location
Cell membrane
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Anti-Tnfrsf23 antibodies

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Target: Tnfrsf23
Host: Rat
Antibody Isotype: IgG
Specificity: Mouse
Clone: CBYJT-3842
Application*: IC, WB
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Submit A Review Fig.3 Signaling pathways in cancers. (Creative Biolabs Authorized) Fig.4 Protocols troubleshootings & guides. (Creative Biolabs Authorized) Submit A Review Fig.3 Signaling pathways in cancers. (Creative Biolabs Authorized) Fig.4 Protocols troubleshootings & guides. (Creative Biolabs Authorized)
For Research Use Only. Not For Clinical Use.
(P): Predicted
* Abbreviations
  • AActivation
  • AGAgonist
  • APApoptosis
  • BBlocking
  • BABioassay
  • BIBioimaging
  • CImmunohistochemistry-Frozen Sections
  • CIChromatin Immunoprecipitation
  • CTCytotoxicity
  • CSCostimulation
  • DDepletion
  • DBDot Blot
  • EELISA
  • ECELISA(Cap)
  • EDELISA(Det)
  • ESELISpot
  • EMElectron Microscopy
  • FFlow Cytometry
  • FNFunction Assay
  • GSGel Supershift
  • IInhibition
  • IAEnzyme Immunoassay
  • ICImmunocytochemistry
  • IDImmunodiffusion
  • IEImmunoelectrophoresis
  • IFImmunofluorescence
  • IGImmunochromatography
  • IHImmunohistochemistry
  • IMImmunomicroscopy
  • IOImmunoassay
  • IPImmunoprecipitation
  • ISIntracellular Staining for Flow Cytometry
  • LALuminex Assay
  • LFLateral Flow Immunoassay
  • MMicroarray
  • MCMass Cytometry/CyTOF
  • MDMeDIP
  • MSElectrophoretic Mobility Shift Assay
  • NNeutralization
  • PImmunohistologyp-Paraffin Sections
  • PAPeptide Array
  • PEPeptide ELISA
  • PLProximity Ligation Assay
  • RRadioimmunoassay
  • SStimulation
  • SESandwich ELISA
  • SHIn situ hybridization
  • TCTissue Culture
  • WBWestern Blot
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