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MAK109

Sigma-Aldrich

LPL Activity Assay Kit

Supplied by Roar Biomedical, Inc.

Synonym(s):

Lipoprotein lipase activity assay kit

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1 KIT
$747.00

$747.00


Estimated to ship onMarch 29, 2025


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1 KIT
$747.00

About This Item

UNSPSC Code:
12161503
NACRES:
NA.84

$747.00


Estimated to ship onMarch 29, 2025


Request a Bulk Order

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)

General description

Lipoprotein lipase (LPL) hydrolyzes triglycerides associated with VLDL.

Application

LPL Activity Assay Kit may be used for detection of LPL activity in plasma samples of patients with hypertriglyceridemia.[1]

Suitability

Suitable for the measurement of lipoprotein lipase activity in a variety of tissue samples

Principle

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.

related product

Storage Class

10 - Combustible liquids


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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
Ewa Szalowska et al.
Peptides, 32(5), 938-945 (2011-02-22)
GIP receptor knockout mice were shown to be protected from the development of obesity on a high fat diet, suggesting a role of GIP in the development of obesity. In our study we aimed to test the hypothesis if excess
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
Chaofeng Yang et al.
Nutrition & metabolism, 9(1), 94-94 (2012-10-31)
Endocrine FGF19 and FGF21 exert their effects on metabolic homeostasis through fibroblast growth factor receptor (FGFR) and co-factor betaKlotho (KLB). Ileal FGF19 regulates bile acid metabolism through specifically FGFR4-KLB in hepatocytes where FGFR1 is not significant. Both FGF19 and FGF21
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

Protocols

Lipoprotein lipase (LPL) hydrolyzes triglycerides associated with VLDL.

Questions

1–2 of 2 Questions  
  1. Which plates are compatible with the MAK109 LPL Activity Assay Kit? Will it work on flat-bottom plates and if the plate has black walls but a clear bottom?

    1 answer
    1. The assay does work on flat-bottom plates, but round-bottom plates are preferred for incubation in a water bath to ensure even temperature distribution in each well. The suitability may depend on the specific activity of the protein.
      It is not recommended to use clear bottom plates for fluorescence-based assays, nor is reading a fluorescent method from the bottom of the plate advisable. The black-walled, clear bottom plates are typically used for visualization with a microscope.

      Helpful?

  2. Is the kit designed for all LPL? Can it provide any selectivity for different types of LPL, such as pancreatic lipase, hepatic lipase, and endothelial lipase?

    1 answer
    1. The substrate could be hydrolyzed by any surface active lipase, offering no selectivity. However, the liquid crystalline physical state of the emulsion provides selectivity for LPL and hepatic lipase (HL). Running post heparin plasma in high salt to inhibit LPL, but not HL, allows for selective activity measurement of LPL or HL. Endothelial lipase (EL) would not be interested in this substrate.

      Helpful?

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