Directly visualize and quantify apoptosis with any cell line or transgenic mouse expressing firefly luciferase.
This one-step assay will detect NanoLuc® Luciferase, an all new, state-of-the-art technology offering unrivaled sensitivity and versatility in a very small reporter.
A simple, sensitive "add-mix-read" firefly luciferase reporter assay. Provides long-lived luminescence ideal for batch processing multiple 96-, 384- or 1,536-well plates.
The ONE-Glo™ + Tox Assay combines luciferase assay chemistry with a cell viability marker to better understand reporter gene expression in the context of cell health.
This assay offers the brightest, most sensitive option for mix-and-read detection of firefly luciferase. It is compatible with high-throughput formats, especially when used in a continuous process format.
This homogeneous reagent system offers fast and simple quantitation of cotransfected firefly and Renilla luciferase activities.
State-of-the-art reporter technology offering unrivaled sensitivity and versatility in a very small luciferase. Find the pNL reporter that is right for your application.
Express firefly and NanoLuc® luciferases from the same transcript. Generate two unfused luciferase enzymes with distinct compound interaction profiles, allowing convenient identification of true and false hits in HTS compound screening.
Quantitatively measure microRNA activity with a luciferase reporter. The firefly luciferase (luc2) vector is the primary reporter to monitor mRNA regulation and Renilla luciferase (hRluc-neo) acts as a control reporter for normalization and selection.
These next generation, luciferase reporter vectors offer more efficient expression of both firefly and Renilla luciferases in mammalian cells.
Generate more relevant data with efficient transfection of your optimal cell line without compromising cell viability.
FuGENE® 6 offers proven performance cited in thousands of scientific papers and used in hundreds of cell lines. The novel non-liposomal formulation offers high efficiency transfection of DNA with minimal toxicity.
Transfect DNA into a wide variety of cell lines with high efficiency and low toxicity! There is no need to remove serum or culture medium after introducing the reagent:DNA complex.
Spend less time optimizing transfections especially for primary cell cultures requiring continuous exposure to serum.
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