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AB185433

Lipolysis Assay试剂盒(Colorimetric)

Lipolysis Assay Kit (Colorimetric)

5

(1 Review)

|

(16 Publications)

Lipolysis Assay Kit (Colorimetric) ab185433 uses a simple and robust way to measure the amount of glycerol released from cells during lipolysis.

- BIOVISION® assay kit
- Individual kit components also available for purchase with a minimum order of 20 units. Contact us to discuss your needs.
3 Images
Functional Studies - Lipolysis Assay Kit (Colorimetric) (AB185433)
  • FuncS

Supplier Data

Functional Studies - Lipolysis Assay Kit (Colorimetric) (AB185433)

Measurement of glycerol level in media of 3T3-L1 cells.

50 μl of 3T3-L1 cells treated with vehicle control (H2O) or 100 nM Isoproterenol for 0-3 hours.

Functional Studies - Lipolysis Assay Kit (Colorimetric) (AB185433)
  • FuncS

Supplier Data

Functional Studies - Lipolysis Assay Kit (Colorimetric) (AB185433)

Glycerol Standard Curve

Schematic Diagram - Lipolysis Assay Kit (Colorimetric) (AB185433)
  • Schematic Diagram

Supplier Data

Schematic Diagram - Lipolysis Assay Kit (Colorimetric) (AB185433)

Representative image of Lipolysis Assay Kit (Colorimetric) ab185433

Components shown from left to right :

- OxiRed Probe

- Isoproterenol

- Glycerol Standard

- Enzyme Mix VI

- Assay Buffer 5

- Buffer IV

- Wash Buffer VIII

Note : The vial labels shown in this image use generic names for illustrative purposes only and may not exactly match the specific component names included in the kit.

Note : Colors of solutions in image may not precisely match the shade of colors in the actual kit.

关键信息

检测方法

Colorimetric

样品类型

Cell culture supernatant

灵敏度

< 0.2 nmol/well

范围

2 - 10 nmol/well

检测时间

40m

检测平台

Microplate reader

产品详情

The lipolysis assay is used to quantify glycerol that is released, along with free fatty acids, from cells during lipolysis. The glycerol and free fatty acids are formed in lipolysis when triglycerides are hydrolyzed.

Lipolysis Assay Kit ab185433 includes:

- the reagents to perform a glycerol assay, with a readout on a colorimetric plate reader

- washing and incubation buffers to use with cultured cells during a lipolysis treatment study

- isoproterenol to use as a positive control to stimulate lipolysis

How the lipolysis assay works

In the lipolysis assay protocol, cultured cells are washed with the supplied buffer, and then incubated either with the incubation buffer and isoproterenol, or in the conditions of your choice. Cell culture media is then collected for the glycerol assay.

In the glycerol assay, glycerol kinase phosphorylates glycerol; and then glycerol phosphate oxidase oxidizes glycerol-1-phosphate to produce dihydroxyacetone phosphate and hydrogen peroxide. The hydrogen peroxide reacts with a probe via a peroxidase to generate color (absorbance λ= 570 nm). The increase in absorbance is proportional to the amount of glycerol in the sample.

Lipolysis assay protocol summary:

- Wash cultured cells

- Incubate cells to stimulate lipolysis

- Transfer cell culture media to 96-well plate

- Add reaction mix

- Incubate for 30 min at room temperature

- Analyze with microplate reader

Related and recommended products

For fluorometric detection, we recommend Lipolysis Assay Kit (Fluorometric) ab185434

The glycerol assay used in this kit, is also sold separately as Free Glycerol Assay Kit ab65337.

Other notes

This product is manufactured by BioVision, an Abcam company and was previously called K577 Lipolysis (3T3-L1) Colorimetric Assay Kit. K577-100 is the same size as the 100 test size of ab185433.

Lipolysis is the hydrolysis of triglycerides within the cell into glycerol and free fatty acids. The glycerol and free fatty acids are then released into the bloodstream or culture media. Lipolysis occurs in essentially all cells, but is most abundant in white and brown adipose tissue. Deficiencies in lipolysis lead to increased intracellular lipid accumulation, resulting in abnormal cellular physiology, hyperlipidemia, and insulin resistance. Lipolysis can be induced by catecholamine and certain hormones. The kit includes synthetic catecholamine, Isoproterenol, which activates ß-adrenergic receptors. This leads to activation of adenylate cyclase, which catalyzes the conversion of ATP to cAMP. cAMP then serves as a second messenger to activate hormone-sensitive lipase, which hydrolyzes the triglycerides. This pathway can be inhibited by insulin.

REACH authorisation
Abcam has not and does not intend to apply for the REACH Authorisation of customers' uses of products that contain European Authorisation list (Annex XIV) substances.
It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.

规格

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性能和储存信息

运输条件
Blue Ice
推荐的短期储存条件
-20°C
推荐的长期储存条件
-20°C
储存信息
-20°C

产品实验方案

靶点信息

文献 (16)

Recent publications for all applications. Explore the full list and refine your search

Revista brasileira de farmacognosia : orgao oficial da Sociedade Brasileira de Farmacognosia 33:334-343 PubMed36819090

2023

Quercetin-3--rutinoside from Downregulates Adipogenesis and Lipid Accumulation and Improves Glucose Uptake by Activation of AMPK/Glut-4 in 3T3-L1 Cells.

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Muni Swamy Ganjayi,Reddy Sankaran Karunakaran,Sreedevi Gandham,Balaji Meriga

Clinical and translational medicine 12:e1108 PubMed36480426

2022

Myoglobin-mediated lipid shuttling increases adrenergic activation of brown and white adipocyte metabolism and is as a marker of thermogenic adipocytes in humans.

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Lisa Christen,Helen Broghammer,Inka Rapöhn,Kevin Möhlis,Christian Strehlau,Aleix Ribas-Latre,Claudia Gebhardt,Lisa Roth,Kerstin Krause,Kathrin Landgraf,Antje Körner,Kerstin Rohde-Zimmermann,Anne Hoffmann,Nora Klöting,Adhideb Ghosh,Wenfei Sun,Hua Dong,Christian Wolfrum,Tienush Rassaf,Ulrike B Hendgen-Cotta,Michael Stumvoll,Matthias Blüher,John T Heiker,Juliane Weiner

Metabolites 11: PubMed34564426

2021

Anti-Obesity Effect of Hot Water Extract of Barley Sprout through the Inhibition of Adipocyte Differentiation and Growth.

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Myeong-Jin Kim,Hye-Won Kawk,Sang-Hyeon Kim,Hyo-Jae Lee,Ji-Won Seo,Jong-Tae Kim,Seung-Hee Jang,Min-Jeong Kim,Young-Min Kim

Frontiers in endocrinology 12:698621 PubMed34394003

2021

Laminin-α4 Is Upregulated in Both Human and Murine Models of Obesity.

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Anna Goddi,Alanis Carmona,Liesl Schroedl,Jeremy M White,Matthew J Piron,Avelino De Leon,Isabel Casimiro,Alexandria Hoffman,Maria A Gonzalez Porras,Eric M Brey,Matthew J Brady,Ronald N Cohen

Frontiers in pharmacology 12:704074 PubMed34366856

2021

Anti-Obesity and Lipid Lowering Activity of Bauhiniastatin-1 is Mediated Through PPAR-γ/AMPK Expressions in Diet-Induced Obese Rat Model.

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Reddy Sankaran Karunakaran,Oruganti Lokanatha,Ganjayi Muni Swamy,Chintha Venkataramaiah,Muppuru Muni Kesavulu,Chippada Appa Rao,Kameswara Rao Badri,Meriga Balaji

Cells 10: PubMed34066961

2021

SIRT5 Inhibition Induces Brown Fat-Like Phenotype in 3T3-L1 Preadipocytes.

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Francesca Molinari,Alessandra Feraco,Simone Mirabilii,Serena Saladini,Luigi Sansone,Enza Vernucci,Giada Tomaselli,Vincenzo Marzolla,Dante Rotili,Matteo A Russo,Maria Rosaria Ricciardi,Agostino Tafuri,Antonello Mai,Massimiliano Caprio,Marco Tafani,Andrea Armani

3 Biotech 11:233 PubMed33968577

2021

A bioactive fraction of inhibits adipogenesis and inflammation in 3T3-L1 cells via modulation of PPAR-γ/SREBP-1c and TNF-α/IL-6.

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Species

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Karunakaran Reddy Sankaran,Muni Swamy Ganjayi,Lokanatha Oruganti,Appa Rao Chippada,Balaji Meriga

Adipocyte 10:216-231 PubMed33866927

2021

Cleavage of the vaspin N-terminus releases cell-penetrating peptides that affect early stages of adipogenesis and inhibit lipolysis in mature adipocytes.

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Species

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Catherine A Tindall,Estelle Erkner,Jan Stichel,Annette G Beck-Sickinger,Anne Hoffmann,Juliane Weiner,John T Heiker

Nature metabolism 3:244-257 PubMed33619378

2021

The major cap-binding protein eIF4E regulates lipid homeostasis and diet-induced obesity.

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Species

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Crystal S Conn,Haojun Yang,Harrison J Tom,Kenji Ikeda,Juan A Oses-Prieto,Hieu Vu,Yasuo Oguri,Supna Nair,Ryan M Gill,Shingo Kajimura,Ralph J DeBerardinis,Alma L Burlingame,Davide Ruggero

The Biochemical journal 477:2735-2754 PubMed32648926

2020

MAPK-interacting kinase 2 (MNK2) regulates adipocyte metabolism independently of its catalytic activity.

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Unspecified application

Species

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James E Merrett,Jianling Xie,Peter J Psaltis,Christopher G Proud
View all publications
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