FXR Agonist Assay Kit (TR-FRET)

Catalog #
78131
$715 *
Size: 384 reactions
Qty
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Description

The FXR (Farnesoid X Receptor) Agonist Assay Kit (TR-FRET) is designed to measure binding of the FXR and SRC-1 (Steroid Receptor Coactivator 1) for screening FXR agonists using TR-FRET technology. With this homogeneous kit, the FXR agonist assay can be performed by adding all materials, including the detection reagents, to the wells and incubating the plate for 2-hours at room temperature followed by reading the TR-FRET signal.

Assay Principle

Assay Principle

Upon binding of the agonist to the FXR, SRC-1-Biotin and FXR form a heterodimer, resulting in energy transfer from Tb donor to the dye labeled acceptor.

Synonyms
Nuclear Receptor Subfamily 1 Group H Member 4 kit, Bile Acid Receptor Assay, RIP14 assay kit, HRR1 assay kit
Product Info
Storage and Usage
Citations
Assay Kit Format
TR-FRET
Species
Human
Supplied As
384 reaction format
Materials Required But Not Supplied

Adjustable micropipettor and sterile tips
Microplate centrifuge

Format
Catalog Name Amount Storage
100410 FXR, GST-tag 3 µg -80°C
  SRC-1, Biotin labeled (10 μM in DMSO) 20 µl -80°C
  CDCA (10 mM in DMSO) 50 µl -20°C
  FXR Binding Buffer 20 ml -20°C
  Tb donor 2 x 10 µl -20°C
  Dye labeled acceptor 2 x 10 µl -20°C
79969 384-well plate, white, nonbinding 1 EA Room
Temp
UniProt #
Q96RI1
Background

Nonalcoholic fatty liver disease (NAFLD) is a characterized by the aberrant accumulation of triglycerides in hepatocytes, even in the absence of significant alcohol consumption or viral infection. The FXR is a nuclear receptor that maintains bile acid homeostasis, and aberrant bile acid signaling via activation of FXR contributes liver disease. Several small molecule agonists have been developed and tested in clinical trials for NASH (Non-Alcoholic SteatoHepatitis), and the FXR pathway is also a molecular target in the search for novel cholesterol lowering agents.

References

1. Angela D., et al. Targeting Bile Acid Receptors: Discovery of a Potent and Selective Farnesoid X Receptor Agonist as a New Lead in the Pharmacological Approach to Liver Diseases. Front Pharmacol. 2017; 8(162):1-13.
2. Sills M., et al. A Comparison of ALPHAScreen, TR-FRET, and TRF as Assay Methods for FXR Nuclear Receptors. J Biomol Screen. 2002; 7(1):3-10