说明书：

EAPL.pdf

Application

• For quantitative assay of adipolysis and evaluation of drug effects on adipolysis.

Key Features

• Sensitive and accurate. Use as little as 10 μL samples. Linear detection range in 96-well plate: 0.92 to 100 μg/mL (10 to 1000 μM) glycerol for colorimetric assays and 0.2 to 5 μg/mL for fluorimetric assays.
• Rapid and convenient.The procedure involves addition of a single working reagent and incubation for 20 min at room temperature.
• Robust and amenable to HTS assays. Potential interference by testing drugs is greatly reduced at 570nm. Compatible with culture media containing phenol red. Assays can be performed in 96 or 384-well plates.

Method

•  OD570nm, or FL530/585nm

Samples

•  Cell culture media

Species

•  All

Size

•  200 tests

Detection Limit

•  0.92 μg/mL

Shelf Life

•  12 months

More Details

•  Obesity is a chronic condition that develops from storage of excessive energy in the form of adipose tissue. The resulting adiposity presents a high risk factor for diseases such as type 2 diabetes, cardiovascular diseases, and cancer. ADIPOLYSIS or lipolysis is a highly regulated process in fat metabolism, in which triglycerides are broken down into glycerol and free fatty acids. Rapid, robust and accurate procedures for adipolysis quantification in cell culture are very useful in research and drug discovery. BioAssay Systems adipolysis assay kit directly measures glycerol released during adipolysis. This homogeneous assay uses a single Working Reagent that combines glycerol kinase, glycerol phosphate oxidase and color reactions in one step. The color intensity of the reaction product at 570nm is directly proportional to glycerol concentration in the sample.

·相关文献

Huttala, Outi, et al (2019). Presence of vasculature results in faster insulin response in adipocytes in vascularized adipose tissue model. ALTEX-Alternatives to animal experimentation. Assay: Adipolysis in human adipose tissue.

Jocken, Johan WE, et al (2018). Short-chain fatty acids differentially affect intracellular lipolysis in a human white adipocyte model. Frontiers in endocrinology 8: 372. Assay: Adipolysis in human stem cell.

Wang, Rebecca Y., et al (2017). Development of a three-dimensional adipose tissue model for studying embryonic exposures to obesogenic chemicals. Annals of biomedical engineering 45.7: 1807-1818. Assay: Adipolysis in human tissues.

Zheng, Qiantao, et al (2017). Reconstitution of UCP1 using CRISPR/Cas9 in the white adipose tissue of pigs decreases fat deposition and improves thermogenic capacity. Proceedings of the National Academy of Sciences 114.45: E9474-E9482. Assay: Adipolysis in pig tissues.

Huttala, Outi, et al (2016). Differentiation of human adipose stromal cells in vitro into insulin-sensitive adipocytes. Cell and tissue research 366.1: 63-74. Assay: Adipolysis in human cells.

Kim, Hyo Joon, et al (2016). An apolipoprotein B100 mimotope prevents obesity in mice. Clinical Science 130.2: 105-116. Assay: Adipolysis in mouse cells.

Yuan, Xiaoxue, et al (2016). Rutin ameliorates obesity through brown fat activation. The FASEB Journal 31.1: 333-345. Assay: Adipolysis in mouse cells.

Chandrasekaran V., Amit A. et al (2013). Effect of Nelumbo nucifera Petal Extracts on Lipase, Adipogenesis, Adipolysis, and Central Receptors of Obesity. Evidence-Based Complementary and Alternative Medicine. 2013: 10.1155/2013/145925 Assay: Adipolysis in cell lines.

Li R et al (2012). Neuropeptide Y potentiates beta-adrenergic stimulation of lipolysis in 3T3-L1 adipocytes. Regul Pept. 178(1-3):16-20. Assay: Adipolysis in mouse adipocytes.