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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 (59) and LIPG Proteins (24) and many more products for this protein.
Showing 10 out of 201 products:
Human Monoclonal LIPG Primary Antibody for ELISA, WB - ABIN394686
Hu, Lui, Mak, Chu, Lee, Poon, Tsui, Ko, Baum, Tam, Li, Tomlinson: Pharmacogenetic analysis of lipid responses to rosuvastatin in Chinese patients. in Pharmacogenetics and genomics 2010
Show all 5 references for ABIN394686
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 references for ABIN316341
Human Polyclonal LIPG Primary Antibody for ELISA, WB - ABIN308446
Jin, Wang, Millar, Quertermous, Rothblat, Glick, Rader: Hepatic proprotein convertases modulate HDL metabolism. in Cell metabolism 2007
Cow (Bovine) Polyclonal LIPG Primary Antibody for IHC, WB - ABIN2779368
Willer, Sanna, Jackson, Scuteri, Bonnycastle, Clarke, Heath, Timpson, Najjar, Stringham, Strait, Duren, Maschio, Busonero, Mulas, Albai, Swift, Morken, Narisu, Bennett, Parish, Shen, Galan, Meneton, Hercberg, Zelenika, Chen, Li, Scott, Scheet, Sundvall, W: Newly identified loci that influence lipid concentrations and risk of coronary artery disease. in Nature genetics 2008
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.
EL-384A/C polymorphism was significantly associated with the ACS and lipids profile in an elderly Uygur population in Xinjiang.
Results showed that the protein levels of endothelial lipase (EL), NF-kappaB (show NFKB1 Antibodies) p65 (show GORASP1 Antibodies), MAPK p38 (show MAPK1 Antibodies) protein (show RNF19A Antibodies) levels, in addition to the proliferation of umbilical vein endothelial cells (HUVECs), were increased by angiotensin II (AngII).
Genetic studies of patients with early onset of coronary artery disease (CAD (show CAD Antibodies)) in the Chinese Han population show that the EL 584C/T variant is not always involved in the pathogenesis of early-onset CAD (show CAD Antibodies).
The results of the present meta-analysis suggest that the carriers of EL 584 T allele have a higher HDL (show HSD11B1 Antibodies)-C level in Caucasian populations. Whereas, it might not be a protective factor for CHD (show CHDH Antibodies).
Results indicate the spatial consensus catalytic triad "Ser (show SIGLEC1 Antibodies)-Asp (show ASIP Antibodies)-His", a characteristic motif in lipoprotein lipase (show LPL Antibodies), hepatic lipase (show LIPC Antibodies), and endothelial lipase.
EL activity was higher in metabolic syndrome and in obesity. It was negatively associated with high-density lipoprotein-cholesterol and apolipoprotein A-I (show APOA1 Antibodies) in control and metabolic syndrome, respectively.
T allele of LIPG -584C/T polymorphism might play a potential role in the susceptibility to atherogenesis in the Turkish population.
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