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The protein encoded by TNFSF14 is a member of the tumor necrosis factor (TNF) ligand family. Additionally we are shipping TNFSF14 Kits (47) and TNFSF14 Proteins (42) and many more products for this protein.
Showing 10 out of 206 products:
Human Monoclonal TNFSF14 Primary Antibody for FACS - ABIN4897779
Celik, Langer, Stellos, May, Shankar, Kurz, Katus, Gawaz, Dengler: Platelet-associated LIGHT (TNFSF14) mediates adhesion of platelets to human vascular endothelium. in Thrombosis and haemostasis 2007
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Human Monoclonal TNFSF14 Primary Antibody for CyTOF, ELISA (Capture) - ABIN4900484
Wang, Wen, Routy, Bernard, Sekaly, Watts et al.: 4-1BBL induces TNF receptor-associated factor 1-dependent Bim modulation in human T cells and is a critical component in the costimulation-dependent rescue of functionally impaired HIV-specific CD8 T ... in Journal of immunology (Baltimore, Md. : 1950) 2007
Show all 4 Pubmed References
Human Polyclonal TNFSF14 Primary Antibody for ELISA, WB - ABIN4330966
Cohavy, Zhou, Ware, Targan: LIGHT is constitutively expressed on T and NK cells in the human gut and can be induced by CD2-mediated signaling. in Journal of immunology (Baltimore, Md. : 1950) 2005
Human Monoclonal TNFSF14 Primary Antibody for FACS - ABIN4897778
Holmes, Wilson, Black, Benest, Vaz, Tan, Tanavde, Cook: Licensed human natural killer cells aid dendritic cell maturation via TNFSF14/LIGHT. in Proceedings of the National Academy of Sciences of the United States of America 2014
LIGHT is highly expressed and companied with severe inflammations in patients with coronary disease. LIGHT significantly enhanced inflammation response in oxLDL-induced THP-1 (show GLI2 Antibodies) macrophages.
LIGHT and LTBR (show LTBR Antibodies) interaction increases the survival and proliferation of human bone marrow-derived mesenchymal stem cells, and therefore, LIGHT might play an important role in stem cell therapy.
LIGHT, via LTbetaR signaling, may contribute to exacerbation of airway neutrophilic inflammation through cytokine and chemokine (show CCL1 Antibodies) production by bronchial epithelial cells.
LIGHT controls TSLP (show TSLP Antibodies) to drive pulmonary fibrosis.
The tumor necrosis factor (show TNF Antibodies) superfamily molecule LIGHT promotes keratinocyte activity and skin fibrosis.
proliferation and migration would be enhanced in Tca8113 cells with over-expressed TNFSF14
LIGHT, a TNF (show TNF Antibodies) superfamily member, is involved in T-cell homeostasis and erosive bone disease associated with rheumatoid arthritis.
Crystal structures of LIGHT and the LIGHT:DcR3 complex reveal the structural basis for the DcR3 (show TNFRSF6B Antibodies)-mediated neutralization of LIGHT.
regulation by NK cell licensing helps to safeguard against TNFSF14 production in response to healthy tissues.
TNFSF14 has an effect on the activation of basophils and eosinophils interacting with bronchial epithelial cells
Blockade of LIGHT markedly suppressed airway smooth muscle hyperplasia and inflammatory responses, which might be modulated through HVEM (show TNFRSF14 Antibodies)-NFkappaB or c-JUN (show JUN Antibodies) pathways.
The LIGHT (Tumour necrosis factor (show TNF Antibodies) ligand superfamily member 14, TNFSF14)/Lymphotoxin beta-Receptor (show LTBR Antibodies)(LTbeta (show LTB Antibodies)-R) pathway, which is involved in T-cell and macrophage activation, was diminished in plasma and in apoE (show APOE Antibodies)-/-Irs2 (show IRS2 Antibodies)+/-HL-/- atheromas.
LIGHT signalling pathway combined with IFN-gamma (show IFNG Antibodies) induces beta cells apoptosis via an NF-kappaB (show NFKB1 Antibodies)/Bcl2 (show BCL2 Antibodies)-dependent mitochondrial pathway.
Together, these results demonstrate that the LIGHT signaling pathway is not only required for inflammatory cytokine production as part of the host response to chlamydial infection, but also influences the differentiation of CD4 (show CD4 Antibodies)(+) CD25 (show IL2RA Antibodies)(+) FoxP3 (show FOXP3 Antibodies)(+) Treg cells, both of which may be essential for control of C. psittaci respiratory tract infection.
These results expose the relevance of LIGHT/LTbetaR/HVEM (show TNFRSF14 Antibodies) interaction for the potential therapeutic control of the allogeneic immune responses mediated by alloreactive CD8 (show CD8A Antibodies) T cells that can contribute to prolong allograft survival.
Mechanistically, intratumoral LIGHT induces pericyte differentiation and normalization via Rho kinase (show ROCK2 Antibodies) signaling. Minute amounts of LIGHT act in a paracrine fashion to trigger an amplifying cascade involving transforming growth factor beta (TGF-beta) from peri (show POSTN Antibodies)-vascular macrophages.
localized overexpression of Tnfsf14 potently enhances muscle regeneration, and that this regenerative capacity of Tnfsf14 is dependent on Akt (show AKT1 Antibodies) signaling.
LIGHT-HVEM (show TNFRSF14 Antibodies) interactions stimulate IL-12 (show IL12A Antibodies) production by DCs during Leishmania donovani infection. Blockade of LIGHT-LTbetaR interactions dramatically enhanced early anti-parasitic immunity.
The protein encoded by this gene is a member of the tumor necrosis factor (TNF) ligand family. This protein is a ligand for TNFRSF14, which is a member of the tumor necrosis factor receptor superfamily, and which is also known as a herpesvirus entry mediator (HVEM). This protein may function as a costimulatory factor for the activation of lymphoid cells and as a deterrent to infection by herpesvirus. This protein has been shown to stimulate the proliferation of T cells, and trigger apoptosis of various tumor cells. This protein is also reported to prevent tumor necrosis factor alpha mediated apoptosis in primary hepatocyte. Two alternatively spliced transcript variant encoding distinct isoforms have been reported.
tumor necrosis factor ligand superfamily, member 14
, tumor necrosis factor (ligand) superfamily, member 14
, delta transmembrane LIGHT
, herpes virus entry mediator ligand
, herpesvirus entry mediator A
, herpesvirus entry mediator ligand
, herpesvirus entry mediator-ligand
, ligand for herpesvirus entry mediator
, tumor necrosis factor ligand superfamily member 14
, tumor necrosis factor receptor-like 2
, tumor necrosis factor superfamily member LIGHT
, tumor necrosis factor superfamily member 14
, tumor necrosis factor superfamily, member 14