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anti-Human Lipoprotein Lipase Anticorps:
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Cat (Feline) Monoclonal Lipoprotein Lipase Primary Antibody pour ELISA, FACS - ABIN1042621
Peterson, Ayyobi, Ma, Henderson, Reina, Deeb, Santamarina-Fojo, Hayden, Brunzell: Structural and functional consequences of missense mutations in exon 5 of the lipoprotein lipase gene. dans Journal of lipid research 2002
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Cow (Bovine) Polyclonal Lipoprotein Lipase Primary Antibody pour WB - ABIN3043618
Yu, Dai, Chen, Zang, Deng, Liu, Ying: Hypolipidemic and antioxidant activities of polysaccharides from Rosae Laevigatae Fructus in rats. dans Carbohydrate polymers 2013
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Human Monoclonal Lipoprotein Lipase Primary Antibody pour ELISA, WB - ABIN969262
Berk, Johnson, Lee, Zhang, Boozer, Pi-Sunyer, Fried, Albu: Higher post-absorptive skeletal muscle LPL activity in African American vs. non-Hispanic White pre-menopausal women. dans Obesity (Silver Spring, Md.) 2008
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Chicken Monoclonal Lipoprotein Lipase Primary Antibody pour IP, ELISA - ABIN2475333
Peterson, Fujimoto, Brunzell: Human lipoprotein lipase: relationship of activity, heparin affinity, and conformation as studied with monoclonal antibodies. dans Journal of lipid research 1992
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Chicken Monoclonal Lipoprotein Lipase Primary Antibody pour IP, ELISA - ABIN2475335
Chang, Reich, Brunzell, Will: Detailed characterization of the binding site of the lipoprotein lipase-specific monoclonal antibody 5D2. dans Journal of lipid research 1999
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Chicken Monoclonal Lipoprotein Lipase Primary Antibody pour IP, ELISA - ABIN2475334
Hussain, Obunike, Shaheen, Hussain, Shelness, Goldberg: High affinity binding between lipoprotein lipase and lipoproteins involves multiple ionic and hydrophobic interactions, does not require enzyme activity, and is modulated by glycosaminoglycans. dans The Journal of biological chemistry 2000
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Human Polyclonal Lipoprotein Lipase Primary Antibody pour WB - ABIN4331137
Zhang, Cui, Wang, Shang, Qi, Xue, Zhao, Deng, Xie: PPARα/γ agonists and antagonists differently affect hepatic lipid metabolism, oxidative stress and inflammatory cytokine production in steatohepatitic rats. dans Cytokine 2015
nder optimal conditions, the electrochemical DNA biosensor exhibited desirable performance for the determination of rs1801177 (of the lipoprotein lipase )with a wide linearity ranging from 10 fM to 10nM and a relatively low detection limit of 3.33 fM (S/N=3).
A link between the expression of LPL (Montrer LCP1 Anticorps) in the tumor cells and a poor clinical outcome of patients suffering chronic lymphocytic leukemia has been established. (Review)
When her TG levels normalized after incidental use of prednisone, an autoimmune mechanism was suspected. Immunoblot analyses showed the presence of autoantibodies to LPL (Montrer LCP1 Anticorps) in the patient's plasma. Autoantibodies to LPL (Montrer LCP1 Anticorps) decreased by 37% while patient was on prednisone, and by 68% as she subsequently transitioned to hydroxychloroquine monotherapy
Updated LPL (Montrer LCP1 Anticorps) structural models were generated by combining disulfide mapping, computational modeling, and data derived from single-molecule Forster resonance energy transfer. New computational suggest that LPL (Montrer LCP1 Anticorps) may dimerize using an interface that is different from the dimerization interface suggested by crystal packing contacts seen in structures of pancreatic lipase (Montrer PNLIP Anticorps).
This meta-analysis suggested that LPL (Montrer LCP1 Anticorps) HindIII variants were associated with a decreased risk of stroke in the Asian population, but not in the non-Asian population.
LPL (Montrer LCP1 Anticorps) HindIII (+/-) and PvuII (+/-), but not the Ser447Ter, might significantly reduce the risk of ischemic stroke.
apoC-III (Montrer APOC3 Anticorps) potently inhibits triglyceride hydrolysis when LPL (Montrer LCP1 Anticorps) is bound to GPIHBP1 (Montrer GPIHBP1 Anticorps)
The results of this meta-analysis suggested that the LPL (Montrer LCP1 Anticorps) S447X polymorphism is likely to be a protective factor in the development of hypertension.
Sequence variation in Kuwaiti Arabs was compared to other populations and was found to be similar with regards to the number of SNPs, InDels and distribution of the number of variants across the LPL (Montrer LCP1 Anticorps) gene locus and minor allele frequency
Regression analysis revealed significant risk for memory loss that are dependent on age and genetic variants like LPL (Montrer LCP1 Anticorps).
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 (Montrer MYLIP Anticorps)-29b targets LPL and TDG (Montrer TDG Anticorps) genes and regulates apoptosis and triglyceride production in mammary epithelial cells.
apoC-I (Montrer APOC1 Anticorps) and apoC-III (Montrer APOC3 Anticorps) 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 (Montrer ANGPTL4 Anticorps).
ANGPTL4 (Montrer ANGPTL4 Anticorps) 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 (Montrer APOC2 Anticorps).
regions that are responsive to activation by apoC-II (Montrer APOC2 Anticorps)
domain (192-238) is absolutely necessary for apolipoprotein AV (Montrer APOA5 Anticorps) in lipid binding and lipoprotein lipase activation
LPL in the hypothalamus is an important regulator of body weight and glucose homeostasis
These results identify LPL as an important regulator of fatty acid transport to skeletal compartments and demonstrate an intricate functional link between systemic and skeletal fatty acid and glucose metabolism.
mutation of a conserved cysteine in GPIHBP1 (Montrer GPIHBP1 Anticorps) abolishes the ability of GPIHBP1 (Montrer GPIHBP1 Anticorps) to bind LPL
The data suggests that ANGPTL3 (Montrer ANGPTL3 Anticorps) 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 (Montrer ANGPTL3 Anticorps))-lipoprotein lipase (LPL)pathway, and suppressed the expression of HMGCS2 (Montrer HMGCS2 Anticorps) through the increased expression of STAT5b (Montrer STAT5B Anticorps).
physiological changes in adipose tissue ANGPTL4 (Montrer ANGPTL4 Anticorps) expression during fasting and cold resulted in inverse changes in the amount of mature-glycosylated LPL in wild-type mice, but not Angptl4 (Montrer ANGPTL4 Anticorps)(-/-) mice. We conclude that ANGPTL4 (Montrer ANGPTL4 Anticorps) 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 (Montrer GPIHBP1 Anticorps)-coated beads, thereby depleting LPL stores on the surface of adipocytes. We conclude that HSPG (Montrer SDC2 Anticorps)-bound LPL in the interstitial spaces of tissues is mobile, allowing the LPL to move to GPIHBP1 (Montrer GPIHBP1 Anticorps) 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 (Montrer PPARA Anticorps) downstream target genes that are involved in fatty acid beta-oxidation.
This study shows that TNF-alpha (Montrer TNF Anticorps), by a Foxo1 (Montrer FOXO1 Anticorps) dependent pathway, increases the transcription of ANGPTL4 (Montrer ANGPTL4 Anticorps) which is secreted by the cells and causes inactivation of LPL.
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