Firefly Luciferase ATP Assay Kit (#28854) Datasheet Without Images Cell Signaling Technology

For Research Use Only. Not for Use in Diagnostic Procedures.

Product Information

Product Usage Information

Substrate Reagent Preparation:

1. Thaw buffer; equilibrate supplied reagents at room temperature.

2. Reconstitute Firefly Luciferase Reaction Mixture with entire bottle of Cell Lysis Buffer.

3. Mix by gentle inverting.

Directions for Use: Plate cells of interest at specific predetermined cell densities, at 100 μL per well, into the 96-well opaque assay plate. Prepare control wells containing media without cells. It is recommended to run samples in duplicates. Treat cells with compounds of interest and incubate according to desired specifications. Add 100 μL of Firefly Luciferase Reaction Mixture to each well containing cells and media only control wells. Mix contents on an orbital shaker for 2 min, then place on benchtop. Allow the plate to incubate at room temperature for an additional 15 min to stabilize luminescent signal. Obtain results from a plate reader with a Luminometer setting.

Note: Absolute signal may vary by plate reader.

Additional Components Not Supplied:

· White opaque 96-well assay plate (i.e., White MaxiSorp/FluoroNunc 96-well plate, ThermoFisher Scientific #437591)

· Single and multichannel pipettes

· Orbital plate shaker

· Plate reader with Luminometer setting.

Storage

All components in this kit are stable for at least 24 months when stored at -80ºC. After reconstitution of the Firefly Luciferase Reaction Mixture, aliquot into single use aliquots to avoid multiple freeze/thaw cycles. Store at 4ºC for up to a week or -20ºC for up to one month. Protect from light.

Specificity / Sensitivity

The Firefly Luciferase Reaction Mixture is a single reagent for performing ATP assays on cultured cells. The RLU output is directly proportional to the amount of viable cells in the sample. The higher the RLUs, the higher the number of viable cells.

Product Description

The Firefly Luciferase ATP Assay Kit allows cell viability to be measured using luminescence. This assay kit detects and quantifies ATP, an indicator of cell viability, by measuring assay readings in relative light units (RLUs) using a luminometer. This is a highly sensitive, highly stable kit with fast results that produces a stable, glowing signal proportional to the viable cell count. The Firefly Luciferase Reaction Mixture is made up of Firefly Luciferase and D-Luciferin.

Background

Cell viability and proliferation assays are widely used in drug discovery to study growth factors, cytokines, and cytotoxic agents. High throughput screening, in early drug discovery compound screening and in later drug safety and toxicity studies, requires a reliable, sensitive, and simple assay with the ability to analyze a large number of samples. Luminescent cell viability assays using luciferase were developed based on the enzymatic reaction of luciferase oxidizing luciferin, yielding visible light (1). Luciferase isolated from the firefly P. pyralis has been widely used to study cell viability through a multistep reaction that involves ATP (2,3). In contrast to cell proliferation assays, such as radioactive thymidine or BrdU labeling of DNA in live cells followed by quantification of the incorporated thymidine (by quantifying sample radioactivity) or BrdU (using anti-BrdU antibody), the Firefly Luciferase ATP assay does not require radioactive materials, cell fixing, or cell permeabilization. It is a one-step assay procedure requiring the addition of a single reagent directly to cultured cells in growth media; washing and multiple pipetting steps are not necessary.

Species Reactivity

Species reactivity is determined by testing in at least one approved application (e.g., western blot).

Cross-Reactivity Key

H: human M: mouse R: rat Hm: hamster Mk: monkey Vir: virus Mi: mink C: chicken Dm: D. melanogaster X: Xenopus Z: zebrafish B: bovine Dg: dog Pg: pig Sc: S. cerevisiae Ce: C. elegans Hr: horse GP: Guinea Pig Rab: rabbit All: all species expected

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