NFAT Reporter (Luciferase) – THP-1 Cell Line
The NFAT reporter (Luciferase)-THP-1 cell line is designed for monitoring the NFAT (nuclear factor of activated T-cells) signaling pathway in THP-1 cells by measuring luciferase activity. It contains a firefly luciferase gene driven by the NFAT response element located upstream of the minimal TATA promoter. Upon activation by NFAT activators such as Ionomycin, endogenous NFAT transcription factors bind to the DNA response elements, inducing transcription of the luciferase reporter gene.
Interested in screening and profiling inhibitors, or activators of NFAT-mediated signaling pathways without the need to purchase and license the cell line? Check out our Cell Signaling Pathway Screening.
Purchase of this cell line is for research purposes only; commercial use requires a separate license. View the full terms and conditions.
Materials Required for Cell Culture
Name | Ordering Information |
Thaw Medium 2 | BPS Bioscience, #60184 |
Growth Medium 2M | BPS Bioscience, #78181 |
Materials Required for Cellular Assay
Name | Ordering Information |
Ionomycin | Sigma, #I3909 |
PMA | Sigma-Aldrich, #P8139 |
Cyclosporin A | Cayman, #12088 |
Assay Medium: Thaw Medium 2 | BPS Bioscience, #60184 |
Growth Medium 2M | BPS Bioscience, #78181 |
96-well tissue culture treated white clear-bottom assay plate | Corning, #3610 |
ONE-Step™ luciferase assay system | BPS Bioscience, #60690 |
Luminometer |
For best results, it is highly recommended to use these validated and optimized media from BPS Bioscience. Other preparations or formulations of media may result in suboptimal performance.
Thaw Medium 2 (BPS Bioscience, #60184): RPMI1640 medium supplemented with 10% FBS, 1% Penicillin/Streptomycin
Growth Medium 2M (BPS Bioscience, #78181): RPMI1640 medium supplemented with 10% FBS, 1% Penicillin/Streptomycin plus 1 μg/ml of Puromycin
Assay Medium: Thaw Medium 2 (BPS Bioscience, #60184)
The cell line has been screened using the PCR-based Venor®GeM Mycoplasma Detection kit (Sigma-Aldrich, #MP0025) to confirm the absence of Mycoplasma species.
1. Clipstone NA, Crabtree GR. Nature. 1992 Jun 25;357(6380):695-7.
2. Lyakh, L., et al. Mol Cell Biol. 1997 May;17(5):2475-84.