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S1PR3 encodes a member of the EDG family of receptors, which are G protein-coupled receptors. Additionally we are shipping S1PR3 Antibodies (145) and S1PR3 Kits (22) and many more products for this protein.
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Sphingosine-1-phosphate receptor 3 (S1PR3) mediates multiple aspects of the inflammatory response during sepsis.
in breast cancer cells overexpression of S1P3 and its activation by S1P (show MBTPS1 Proteins) has pro-inflammatory and pro-metastatic potential by inducing COX-2 expression and PGE2 signaling via EP2 (show SPAG11B Proteins) and EP4 (show PTGER4 Proteins).
S1PR1 (show S1PR1 Proteins)/3 silencing alters proliferation, adhesion, viability and lateral motility in estrogen receptor (show ESR1 Proteins)-negative MCF-7 and estrogen receptor (show ESR1 Proteins)-positive MDA-MB-231 breast cancer cells.
High S1PR3 expression is associated with increased lung adenocarcinoma.
The S1P1,3 activation results in Akt (show AKT1 Proteins) phosphorylation and subsequent activation of eNOS (show NOS3 Proteins) via phosphorylation at serine(1177) and dephosphorylation at threonine(495).
HDL (show HSD11B1 Proteins)-associated ApoM (show APOM Proteins) is anti-apoptotic by delivering sphingosine 1-phosphate to S1P1 (show S1PR1 Proteins) and S1P3 receptors on vascular endothelium.
The study shows that S1P receptor 3 (S1PR3) mRNA is overexpressed in EBV-positive NPC (show NPC1 Proteins) patient-derived xenografts and a subset of primary NPC (show NPC1 Proteins) tissues, and that knockdown of S1PR3 suppressed the activation of AKT (show AKT1 Proteins) and the S1P (show MBTPS1 Proteins)-induced migration of NPC (show NPC1 Proteins) cells.
S1pr3 promotes leukocyte rolling by mobilization of endothelial P-selectin (show SELP Proteins).
Stimulation with sphingosine-1-phosphate enhances cancer stem cells via S1PR3 and subsequent Notch1 (show NOTCH1 Proteins) activation.
TRPC1 (show TRPC1 Proteins) functions as a major regulator of S1P3 and VEGFR2 (show KDR Proteins) expression.
The absence of S1P3 appears responsible for a lower availability of calcium during fatigue.
These results highlight an important role for S1PR3 in Hematopoietic stem and progenitor cell niche occupancy.
S1P3 deletion protects mouse soleus from age-related drop in muscle mass, force, and regenerative capacity.
The finding that S1P3 receptor- and Galpha13 (show GNA13 Proteins)-mediated RhoA (show RHOA Proteins) activation is responsible for protection against ischemia/reperfusion suggests that selective targeting of S1P3 receptors could provide therapeutic benefits in ischemic heart disease.
The role of the S1PR3/PDGFR-beta (show PDGFRB Proteins)/Akt (show AKT1 Proteins) pathway in sphingosine-1-phosphate -induced endothelial progenitor cells migration and angiogenesis
P2RY8 promotes clustering of activated B cells within follicles in a follicular dendritic cell (FDC)-dependent manner.
Smad3 (show SMAD3 Proteins) deficiency leads to mandibular condyle degradation via the sphingosine 1-phosphate (S1P (show S1PR1 Proteins))/S1P3 signaling axis
CTGF (show CTGF Proteins) exerts profibrotic action in myoblasts via the up-regulation of sphingosine kinase-1 (show SPHK1 Proteins)/S1P3 signaling axis in TGF-beta (show TGFB1 Proteins) dependent manner.
This gene encodes a member of the EDG family of receptors, which are G protein-coupled receptors. This protein has been identified as a functional receptor for sphingosine 1-phosphate and likely contributes to the regulation of angiogenesis and vascular endothelial cell function.
sphingosine-1-phosphate receptor 3
, sphingosine 1-phosphate receptor 3-like
, G protein-coupled receptor, endothelial differentiation gene-3
, S1P receptor 3
, S1P receptor EDG3
, S1P receptor Edg-3
, endothelial differentiation G-protein coupled receptor 3
, endothelial differentiation, sphingolipid G-protein-coupled receptor, 3
, sphingosine 1-phosphate receptor 3
, sphingosine 1-phosphate receptor Edg-3
, S1p receptor 3
, endothelial differentiation sphingolipid G-protein-coupled receptor 3
, lysophospholipid receptor B3