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Receptor for an unknown ligand. Additionally we are shipping G Protein-Coupled Receptor 132 Antibodies (55) and many more products for this protein.
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we found an additional novel G2A variant (G2A-b) that is the major transcript with functional response to ligand stimulation as well as G2A-a, and succeeded in discriminating proton-sensing and oxidized fatty acid-sensing activities of G2A.
G2A is a negative modifier of lymphoid leukemogenesis initiated by the BCR-ABL oncogene
In atherosclerotic plaques of human coronary arterial specimens, G2A is expressed by macrophages within the lipid-r (show APOE Proteins)ich plaques, whereas no immunoreactivity of G2A is observed in fibrous plaques where macrophages do not exist.
G2A can activate a specific combination of G proteins, and G2A/LPC (show PCSK7 Proteins)-induced apoptosis involves both G alpha(13 (show GNA13 Proteins))- and G alpha(s (show GNAS Proteins))-mediated pathways
G2A was not detected in either brain or skin vascular endothelial cell type.
G2A is a proton-sensing G-protein-coupled receptor (show ADRA1A Proteins) antagonized by lysophosphatidylcholine
Activity of the human G2A receptor is less sensitive to pH fluctuations as measured by inositol phosphate and cAMP accumulation.
results indicate that G protein-coupled receptor G2A is a receptor for 9-hydroxyoctadecadienoic acid (9-HODE) and other oxidized free fatty acids and is activated by oxidized free fatty acids
G2A latent within neutrophil secretory vesicles may facilitate signaling through lysophospholipids for neutrophil activation and calcium flux.
9-HODE-G2A signaling plays proinflammatory roles in skin under oxidative conditions
Lyso-PS signaled to macrophages in a G2A-dependent manner for their enhanced production of prostaglandin E2 (PGE2) via a calcium-dependent cytosolic phospholipase A2 (show PLA2G4A Proteins)/cyclooxygenase-mediated mechanism.
G2A is expressed predominantly by macrophages within atherosclerotic lesions at the aortic root of apolipoprotein E (show APOE Proteins)-deficient mice.
role of G2A in lysophosphatidylcholine-mediated T-cell migration
G2A signaling regulates macrophage chemotaxis to lysophosp[hatidylcholine.
data indicate the ability of lysophosphatidylcholine to stimulate macrophage & T-cell chemotaxis via G2A is not manifested in vivo & G2A-mediated proapoptotic rather than chemotactic action is most penetrant during atherogenesis
the neuritogenic effect of sPLA2 is mediated by generation of LPC and subsequent activation of G2A
Examination of lipoprotein profiles revealed elevated levels of circulating high-density lipoprotein (HDL (show HSD11B1 Proteins)) cholesterol in G2A-/- LDLR (show LDLR Proteins)-/- mice compared with their G2A+/+ LDLR (show LDLR Proteins)-/- counterparts after extended periods of diet intervention.
Endothelial G2A expression may aid in prevention of vascular inflammation and atherosclerosis.
The G2A receptor is important for hepatobiliary bile salt, cholesterol, and phospholipid homeostasis and for the pathogenesis of cholesterol gallstone formation.
NADPH oxidase-dependent generation of lysophosphatidylserine enhances clearance of activated and dying neutrophils via G2A.
Receptor for an unknown ligand. Activates a G alpha protein, most likely G alpha(q). May be involved in apoptosis. Functions at the G2/M checkpoint to delay mitosis. May serve as a mechanism for T- and B-cells, and other cell types, to slow their proliferation and repair damaged DNA to ensure proper replication.
G protein-coupled receptor 132
, probable G-protein coupled receptor 132-like
, G2 accumulation protein
, probable G-protein coupled receptor 132
, G protein-coupled receptor G2A
, G protein-coupled receptor G2a