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The protein encoded by LIPG has substantial phospholipase activity and may be involved in lipoprotein metabolism and vascular biology. Additionally we are shipping LIPG Kits (47) and LIPG Proteins (16) and many more products for this protein.
Showing 10 out of 193 products:
Human Polyclonal LIPG Primary Antibody for ICC, IHC (fro) - ABIN152888
Nijstad, Wiersma, Gautier, van der Giet, Maugeais, Tietge: Scavenger receptor BI-mediated selective uptake is required for the remodeling of high density lipoprotein by endothelial lipase. in The Journal of biological chemistry 2009
Show all 6 Pubmed References
Human Polyclonal LIPG Primary Antibody for ELISA, WB - ABIN316341
Gauster, Hiden, Blaschitz, Frank, Lang, Alvino, Cetin, Desoye, Wadsack: Dysregulation of placental endothelial lipase and lipoprotein lipase in intrauterine growth-restricted pregnancies. in The Journal of clinical endocrinology and metabolism 2007
Show all 2 Pubmed References
Human Polyclonal LIPG Primary Antibody for ICC, IF - ABIN152895
Edmondson, Brown, Kathiresan, Cupples, Demissie, Manning, Jensen, Rimm, Wang, Rodrigues, Bamba, Khetarpal, Wolfe, Derohannessian, Li, Reilly, Aberle, Evans, Hegele, Rader: Loss-of-function variants in endothelial lipase are a cause of elevated HDL cholesterol in humans. in The Journal of clinical investigation 2009
Show all 2 Pubmed References
Polyclonal LIPG Primary Antibody for WB - ABIN540696
Wiersma, Gatti, Nijstad, Kuipers, Tietge: Hepatic SR-BI, not endothelial lipase, expression determines biliary cholesterol secretion in mice. in Journal of lipid research 2009
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Human Monoclonal LIPG Primary Antibody for FACS, ICC - ABIN4308194
Ménégaut, Masson, Abello, Denimal, Truntzer, Ducoroy, Lagrost, Pais de Barros, Athias, Petit, Martin, Steinmetz, Kretz: Specific enrichment of 2-arachidonoyl-lysophosphatidylcholine in carotid atheroma plaque from type 2 diabetic patients. in Atherosclerosis 2016
We identified a missense Asn396Ser mutation (rs77960347) in the endothelial lipase (LIPG) gene, occurring with an allele frequency of 1% in the general population, which was significantly associated with depressive symptoms (P-value=5.2 x 10-08, beta=7.2).
the EL 2237 A allele might be associated with an increased Apo (show C9orf3 Antibodies) A1 level in Coronary Artery Disease subjects.
Increased hepatic expression of endothelial lipase attenuates cholesterol diet-induced hypercholesterolemia and protects against atherosclerosis.
Endothelial lipase is upregulated in human umbilical vein endothelial cells by interleukin-6 (show IL6 Antibodies) partly via the p38 MAPK (show MAPK14 Antibodies) and p65 NF-kappaB (show NFkBP65 Antibodies) signaling pathways.
Endothelial lipase (EL) 2037T/C and 2237 G/A polymorphisms might not affect the lipid-owing effects of rosuvastatin in Chinese coronary artery disease patients
Endothelial lipase protein (show ABHD6 Antibodies) expression was increased in skeletal muscle of middle-aged men with high oxygen consumption.
LIPG Polymorphisms are associated with Hyperlipidemia.
FoxA1 (show FOXA1 Antibodies), FoxA2 (show FOXA2 Antibodies), and LIPG control the uptake of extracellular lipids for breast cancer growth.
results suggested that the SNP -384A/C in the LIPG gene may be associated with risk for coronary artery disease(CAD)and the LIPG gene may play a role in CAD in the Han Chinese
Studied if a specific variant of the endothelial lipase gene was more specifically linked to the severity of diabetic retinopathy.
Brain capillary endothelial cells synthesize and secrete endothelial lipase (EL); EL can generate fatty acids at blood-brain barrier for transport to deeper regions of the brain as building blocks for membrane phospholipids.
inhibitory activity of AOE on pancreatic lipase (show PNLIP Antibodies) enzyme was evaluated at concentrations from 60 to 1000 mug/mL. The AOE inhibited the pancreatic lipase (show PNLIP Antibodies) with an IC50 = 588.5 mug/mL
Hepatic lipase (show LIPC Antibodies) and endothelial lipase influence molecular species of several classes of plasma lipids.
Furin (show FURIN Antibodies) has a role as the primary in vivo convertase of ANGPTL3 (show ANGPTL3 Antibodies) and endothelial lipase in hepatocytes
The role of EL in HDL (show HSD11B1 Antibodies)-associated S1P (show S1PR1 Antibodies) effects provides new insights into EL action, the responses seen through EL and HDL (show HSD11B1 Antibodies) interaction, and S1P (show S1PR1 Antibodies) signaling.
Endothelial lipase may act as an alternative candidate to provide fatty acids to the heart and regulate cardiac function.
Hepatic lipase (show LIPC Antibodies)- and endothelial lipase-deficiency in mice promotes macrophage-to-feces RCT (show FOXE3 Antibodies) and HDL (show HSD11B1 Antibodies) antioxidant properties.
Endothelial lipase supplies cells with free fatty acids and HDL (show HSD11B1 Antibodies)-derived lysophosphatidylcholine and lysophosphatidylethanolamine species resulting in increased cellular triglycerides and phosphatidylcholine (show SGMS2 Antibodies) (PC) content and decreased PC synthesis.
EL expression modulates vascular remodeling as well as plasma HDL (show HSD11B1 Antibodies)-C levels
Starvation regulates endothelial lipase expression via SREBP-2 (show SREBF2 Antibodies).
The protein encoded by this gene has substantial phospholipase activity and may be involved in lipoprotein metabolism and vascular biology. This protein is designated a member of the TG lipase family by its sequence and characteristic lid region which provides substrate specificity for enzymes of the TG lipase family.
, lipase, endothelial
, endothelial lipase-like
, Endothelial lipase
, endothelial cell-derived lipase
, lipoprotein lipase H
, lipose, endothelial
, endothelial-derived lipase
, lipase G