Nuclear Factor of Activated T cells (NFAT)
|Product Family||Product Number||Product Description||Technical Manual|
|IB18001-32||NFAT Reporter Assay System, 3 x 32 assays in 96-well format||Technical Manual|
|IB18001||NFAT Reporter Assay System, 1 x 96-well format assays||Technical Manual|
|IB18002||NFAT Reporter Assay System, 1 x 384-well format assays|
Nuclear Factor of Activated T cells Assay Kit
This Nuclear Factor of Activated T cells (NFAT) assay kit is an all-inclusive firefly luciferase reporter assay system that includes addition to NFAT Reporter Cells, two optimized media for use during cells culture and in diluting test samples, the calcineurin-NFAT pathway activator Ionomycin, Luciferase Detection Reagent, and a cell culture-ready assay plate.
NFAT Reporter Cells are transiently transfected and prepared as frozen stocks using INDIGO's proprietary CryoMite™ process. This cryo-preservation method allows for the immediate dispensing of healthy, division-competent reporter cells into assay plates. There is no need for cumbersome intermediate treatment steps such as spin-and-rinse of cells, viability determinations, or cell titer adjustments prior to assay setup.
INDIGO’s NFAT assay kits feature a luciferase detection reagent specially formulated to provide stable light emission between 5 and 90+ minutes after initiating the luciferase reaction. Incorporating a 5-minute reaction-rest period ensures that light emission profiles attain maximal stability, thereby allowing assay plates to be processed in batch. By doing so, the signal output from all sample wells, from one plate to the next, may be directly compared within an experimental set.
NFAT assay kits are offered in different assay formats to accommodate researchers' needs: 3x 32, 1x 96, and 1x 384 assay formats for screening small numbers of test compounds, as well as custom bulk reagents for HTS applications.
Bulk assay reagents can be custom manufactured to accommodate any scale of HTS. Please inquire.
Nuclear Factor of Activated T cells Assay Services
The primary application of INDIGO's cell-based NFAT assays are to quantitatively assess the bioactivity of a test compound as an agonist or antagonist of the receptor. Service assays include a positive control reference compound and 'vehicle' control for every experiment. A formal study report and all data files are provided to the client upon completion of the study. To receive a quote for your proposed study, complete & submit the online "Request a Quote" form or contact an INDIGO Customer Service Representative to discuss your desired study parameters.
Nuclear Factor of Activated T cells Assay Background
The five members of the Nuclear Factor of Activated T cells (NFAT1-5) family were initially identified as key regulators of genes involved in the activation, proliferation, differentiation, and apoptosis of cells, most notably the T cells and B cells of the immune system.
Inactive NFAT resides in the cytoplasm in a multi-phosphorylated form. Phospho-NFAT is converted to its active form through the activation of calcineurin, a calcium-dependent phosphatase. Any physiological event that drives the influx of extra-cellular Ca+2, or depletes internal Ca+2 stores within the endoplasmic reticula, results in the Ca+2-activation of calcineurin and its subsequent dephosphorylation of phospho-NFAT. Activated NFAT translocates to the nucleus where it binds to specific genetic response element (GRE) sequences within the promoter / enhancer region of target genes. Functional transcription complexes form via cooperative association with other transcription factors, most notably AP-1.
Importantly, dysregulation of the calcineurin-NFAT pathway is strongly associated with autoimmune diseases such as systemic lupus erythematosus and rheumatoid arthritis, thereby making it an important therapeutic target for small molecule drug development.
INDIGO's Reporter Cells contain an engineered luciferase reporter gene functionally linked to tandem NFAT/AP-1 GRE sequences positioned immediately upstream of a minimal promoter. Activated NFAT will bind to its corresponding GREs to initiate the formation of a complete transcription complex that drives Luc gene expression. Thus, quantifying changes in luciferase activity in the treated reporter cells provides a sensitive surrogate measure of changes in NFAT activity. Accordingly, the principal application of this reporter assay is in the screening of test compounds to quantify any functional activities, either activating or inhibitory, that they may exert against the calcineurin-NFAT signal transduction pathway.