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LPL encodes lipoprotein lipase, which is expressed in heart, muscle, and adipose tissue. Additionally we are shipping Lipoprotein Lipase Antibodies (140) and Lipoprotein Lipase Proteins (15) and many more products for this protein.
Showing 10 out of 66 products:
Guinea Pig Lipoprotein Lipase ELISA Kit for Sandwich ELISA - ABIN2345123
Chan, Wong, Pang, Barrett, Watts et al.: Inter-relationships between proprotein convertase subtilisin/kexin type 9, apolipoprotein C-III and plasma apolipoprotein B-48 transport in obese subjects: a stable isotope study in the postprandial ... in Clinical science (London, England : 1979) 2014
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Human Lipoprotein Lipase ELISA Kit for Sandwich ELISA - ABIN414399
Wang, Puthanveetil, Wang, Kim, Abrahani, Rodrigues: Severity of diabetes governs vascular lipoprotein lipase by affecting enzyme dimerization and disassembly. in Diabetes 2011
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Human Lipoprotein Lipase ELISA Kit for Sandwich ELISA - ABIN366804
Levine, Hull, Buchwald, Villablanca: The spontaneous firing patterns of forebrain neurons. II. Effects of unilateral caudate nuclear ablation. in Brain research 1974
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Mouse (Murine) Lipoprotein Lipase ELISA Kit for Sandwich ELISA - ABIN367674
Feng, Hai-ning, Xiao-man, Zun-chen, Sheng-rong, Das: Effect of yellow capsicum extract on proliferation and differentiation of 3T3-L1 preadipocytes. in Nutrition (Burbank, Los Angeles County, Calif.) 2014
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Mouse (Murine) Lipoprotein Lipase ELISA Kit for Sandwich ELISA - ABIN415412
Liu, Xu, Liu, Ding, Liu, Chen, Fan, Zhang, Zheng, Zou, Lyu, Zhang: Regulation of plasma lipid homeostasis by hepatic lipoprotein lipase in adult mice. in Journal of lipid research 2016
heterozygous N291S mutation in the lipoprotein lipase gene impairs whole-body insulin (show INS ELISA Kits) sensitivity and affects a distinct set of plasma metabolites in humans
LPL (show LCP1 ELISA Kits) is important for the maturation of small discoidal HDL (show HSD11B1 ELISA Kits) particles into large spherical HDL (show HSD11B1 ELISA Kits) particles, while HL is important for HDL (show HSD11B1 ELISA Kits) remodeling of very large HDL (show HSD11B1 ELISA Kits) particles into intermediate-size HDL (show HSD11B1 ELISA Kits) particles, as shown in lipoprotein lipase and hepatic lipase (show LIPC ELISA Kits) deficiency
The authors now show: (1) that ANGPTL4 (show ANGPTL4 ELISA Kits) inactivates LPL (show LCP1 ELISA Kits) by catalyzing the unfolding of its hydrolase domain; (2) that binding to GPIHBP1 (show GPIHBP1 ELISA Kits) renders LPL (show LCP1 ELISA Kits) largely refractory to this inhibition; and (3) that both the LU domain and the intrinsically disordered acidic domain of GPIHBP1 (show GPIHBP1 ELISA Kits) are required for this protective effect.
Carrier status for the two common LPL (show LCP1 ELISA Kits) variants: 447Ter (low TG/high HDL (show HSD11B1 ELISA Kits)-C) and 291Ser (high TG/low HDL (show HSD11B1 ELISA Kits)-C) was determined. Compared with the reference variant, the prevalence of metabolic syndrome was lower in carriers of the 447Ter variant (11.2% vs. 17.9%, P < 0.001) but with no difference in carriers of the 291Ser variant (18.4% vs. 16.5%, P = 0.59).
A rare variant in APOC3 (show APOC3 ELISA Kits)(rs138326449) has been associated with triglyceride, very low-density lipoprotein, and high-density lipoprotein levels, as well as risk of coronary heart disease. Effects are unlikely to be solely predictable by the action of APOC3 (show APOC3 ELISA Kits) through LPL (show LCP1 ELISA Kits).
LPL (show LCP1 ELISA Kits) gene polymorphisms are not genetic markers for the development of stroke in the Colombian sample used.
Acute hypoxia strongly inhibits lipoprotein lipase activity in differentiated human preadipocytes.
novel mutations cause type 1 hyperlipoproteinemia by inducing a loss or reduction in LPL (show LCP1 ELISA Kits) secretion accompanied by a loss of LPL (show LCP1 ELISA Kits) enzymatic activity
LPL (show LCP1 ELISA Kits) HindIII polymorphism was significantly associated with the risk of coronary artery disease (CAD (show CAD ELISA Kits)); for Ser447X polymorphism, it was found that only XX genotype was significantly associated with CAD (show CAD ELISA Kits) risk; PvuII polymorphism had no significant association with CAD (show CAD ELISA Kits) risk; LPL (show LCP1 ELISA Kits) HindIII polymorphism might serve as a potential biomarker for CAD (show CAD ELISA Kits) risk
Rare variants in LPL (show LCP1 ELISA Kits) and a common variant in APOA5 (show APOA5 ELISA Kits) were more commonly found in Thai subjects with severe hypertriglyceridemia
isothermal titration calorimetry (ITC) can be used for quantitative measurements of LPL activity and interactions under in vivo-like conditions, for comparisons of the properties of plasma samples from patients and control subjects as substrates for LPL, as well as for testing of drug candidates developed with the aim to affect the LPL system.
miR (show MYLIP ELISA Kits)-29b targets LPL and TDG (show TDG ELISA Kits) genes and regulates apoptosis and triglyceride production in mammary epithelial cells.
apoC-I (show APOC1 ELISA Kits) and apoC-III (show APOC3 ELISA Kits) inhibit lipolysis by displacing LPL from lipid emulsion particles. We also propose a role for these apolipoproteins in the irreversible inactivation of LPL by factors such as angptl4 (show ANGPTL4 ELISA Kits).
ANGPTL4 (show ANGPTL4 ELISA Kits) is more accurately described as a reversible, noncompetitive inhibitor of LPL.
Our findings confirmed that three novel SNPs we identified in the LPL gene can affect fatty acid composition and carcass traits. Therefore, selection for AA and GA genotypes should be recommended to genetically improve beef quality and flavor.
Single nucleotide polymorphisms of the LPL gene might be useful genetic markers for growth traits in the bovine reproduction and breeding.
Results describe the functional role of the secondary structure in the lipoprotein lipase-binding portion of apolipoprotein CII (show APOC2 ELISA Kits).
regions that are responsive to activation by apoC-II (show APOC2 ELISA Kits)
domain (192-238) is absolutely necessary for apolipoprotein AV (show APOA5 ELISA Kits) in lipid binding and lipoprotein lipase activation
The data suggests that ANGPTL3 (show ANGPTL3 ELISA Kits) is part of the machinery causing dyslipidemia majorily via LPL inhibition in mastitis mice.
Using in vitro ketosis model by glucose starvation, studied inhibition of ketosis by momilactone B. Found momilactone B could regulate the angiopoietin-like-3 (ANGPTL3 (show ANGPTL3 ELISA Kits))-lipoprotein lipase (LPL)pathway, and suppressed the expression of HMGCS2 (show HMGCS2 ELISA Kits) through the increased expression of STAT5b (show STAT5B ELISA Kits).
physiological changes in adipose tissue ANGPTL4 (show ANGPTL4 ELISA Kits) expression during fasting and cold resulted in inverse changes in the amount of mature-glycosylated LPL in wild-type mice, but not Angptl4 (show ANGPTL4 ELISA Kits)(-/-) mice. We conclude that ANGPTL4 (show ANGPTL4 ELISA Kits) promotes loss of intracellular LPL by stimulating LPL degradation after LPL processing in the endoplasmic reticulum (ER).
LPL moved quickly from heparan sulfate proteoglycans (HSPGs) on adipocytes to GPIHBP1 (show GPIHBP1 ELISA Kits)-coated beads, thereby depleting LPL stores on the surface of adipocytes. We conclude that HSPG (show SDC2 ELISA Kits)-bound LPL in the interstitial spaces of tissues is mobile, allowing the LPL to move to GPIHBP1 (show GPIHBP1 ELISA Kits) on endothelial cells
our study reveals that hepatic LPL is involved in the regulation of plasma LPL activity and lipid homeostasis.
The induction of LPL activity by fasting in core transgenic mice activated PPARalpha (show PPARA ELISA Kits) downstream target genes that are involved in fatty acid beta-oxidation.
This study shows that TNF-alpha (show TNF ELISA Kits), by a Foxo1 (show FOXO1 ELISA Kits) dependent pathway, increases the transcription of ANGPTL4 (show ANGPTL4 ELISA Kits) which is secreted by the cells and causes inactivation of LPL.
Our findings suggest that neuronal LPL is involved in the regulation of body weight and composition in response to either the change in quantity (HF feeding) or quality (n-3 PUFA-enriched) of dietary fat
An LPL structural model suggests that the LPL S447X truncation exposes residues implicated in LPL binding to lipoprotein binding uptake receptors, such as GPIHBP1 (show GPIHBP1 ELISA Kits).
feeding induces lipasin, activating the lipasin-Angptl3 (show ANGPTL3 ELISA Kits) pathway, which inhibits LPL in cardiac and skeletal muscles to direct circulating TAG to WAT for storage
LPL encodes lipoprotein lipase, which is expressed in heart, muscle, and adipose tissue. LPL functions as a homodimer, and has the dual functions of triglyceride hydrolase and ligand/bridging factor for receptor-mediated lipoprotein uptake. Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia, while less extreme mutations in LPL are linked to many disorders of lipoprotein metabolism.
, O 1-4-5
, adipose lipoprotein lipase
, triacylglycerol lipase