MAK109
LPL Activity Assay Kit
Supplied by Roar Biomedical, Inc.
Synonym(s):
Lipoprotein lipase activity assay kit
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About This Item
NACRES:
NA.84
UNSPSC Code:
12161503
Product Name
LPL Activity Assay Kit, Supplied by Roar Biomedical, Inc.
usage
sufficient for 100 fluorometric tests
application(s)
pharmaceutical
detection method
fluorometric
relevant disease(s)
gastrointestinal diseases; cardiovascular diseases
storage temp.
2-8°C
Gene Information
human ... LPL(4023)
Related Categories
Application
LPL Activity Assay Kit may be used for detection of LPL activity in plasma samples of patients with hypertriglyceridemia.
Suitable for the measurement of lipoprotein lipase activity in a variety of tissue samples
Biochem/physiol Actions
The LPL Activity Assay Kit includes a non-fluorescent substrate emulsion that becomes intensely fluorescent upon interaction with LPL and pre-hydrolyzed substrate for use as a standard to convert the fluorescence intensity reading to moles of reactant formed (λEx=370 nm/λEm=450 nm). The assay is not specific for LPL and will also detect hepatic lipase activity.
General description
Lipoprotein lipase (LPL) hydrolyzes triglycerides associated with VLDL.
Storage Class
10 - Combustible liquids
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Maria Notarnicola et al.
Lipids in health and disease, 11, 145-145 (2012-11-01)
Lipid metabolism is altered in subjects with liver steatosis. FAS is a key enzyme in de novo lipogenesis and both FAS gene expression and enzymatic activity are primarily regulated by metabolic signals in the liver. Lipoprotein lipase (LPL), the rate-limiting
Tomomi Yamazaki et al.
Journal of lipid research, 53(10), 2024-2037 (2012-06-28)
Postprandial hyperlipidemia (lipemia) is a risk factor for atherosclerosis. However, mouse models of postprandial hyperlipidemia have not been reported. Here, we report that ddY mice display marked postprandial hypertriglyceridemia in response to dietary fat. In ddY mice, the fasting serum
Hung-Yu Sun et al.
Gut, 62(8), 1193-1203 (2012-06-13)
Circulating hepatitis C virus (HCV) virions are associated with triglyceride-rich lipoproteins, including very low-density lipoprotein (VLDL) and low-density lipoprotein (LDL), designated as lipo-viro-particles (LVPs). Previous studies showed that lipoprotein lipase (LPL), a key enzyme for hydrolysing the triglyceride in VLDL
Evemie Dubé et al.
Biology of reproduction, 87(1), 14-14 (2012-05-04)
Knowledge of the consequences of maternal obesity in human placental fatty acids (FA) transport and metabolism is limited. Animal studies suggest that placental uptake of maternal FA is altered by maternal overnutrition. We hypothesized that high maternal body mass index
Cedric H L Shackleton
Lipids, 47(1), 1-12 (2011-08-30)
In 1937 Butler and Marrian found large amounts of the steroid pregnanetriol in urine from a patient with the adrenogenital syndrome, a virilizing condition known to be caused by compromised adrenal secretion even in this pre-cortisol era. This introduced the
Protocols
Lipoprotein lipase (LPL) hydrolyzes triglycerides associated with VLDL.
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