Promega's Política de cookies

Empleamos cookies y tecnologías similares para mantener la funcionalidad de nuestro sitio web, analizar su rendimiento, mejorar el funcionamiento y mostrar contenido personalizado. Algunas cookies son esenciales para el buen funcionamiento de nuestro sitio web. El resto no serán instaladas en su equipo sin su consentimiento. Visite la Política de Cookies para obtener mayor detalle.

G4000_CelTiter-96-Non-Radioactive-Cytotoxicity-Assay-1000 G4100_CellTiter-96-NonRadioactive-Cytotoxicity-Assay-5000

A Colorimetric Assay to Assess Cell Viability

  • Greater sensitivity than the neutral red procedure
  • Non-radioactive, fast and convenient assay applicable to a variety of cells

Catalog Number:

Size

Overview
Protocols
Specifications
Resources
Related Products

The CellTiter 96® Non-radioactive Cell Proliferation Assay is a collection of qualified reagents that provide a convenient method of determining viable cell number. The CellTiter 96® Assay is a modification of the MTT assay method described by Mosmann and incorporates several improvements to the method that address previous technical problems including: 1) serum protein precipitation caused by adding organic solvent; 2) interference by phenol red; 3) incomplete solubilization of the formazan crystals resulting in lower sensitivity; and 4) stability of the colored product.

The CellTiter 96® Assay is performed by adding a premixed, optimized Dye Solution to culture wells of a 96-well plate, usually containing various concentrations of growth factor or test substance. During a 4-hour incubation, living cells convert the MTT tetrazolium component of the Dye Solution into a formazan product. If you currently use a [3H]-thymidine incorporation assay, the addition of Dye Solution can be substituted for the pulse of radioactive thymidine at the time point in the assay when the pulse of [3H]-thymidine is usually added. The Solubilization/Stop Solution is then added to the culture wells to solubilize the formazan product, and the absorbance at 570nm is recorded using a 96-well plate reader. In addition, direct comparison between [3H]-thymidine incorporation and tetrazolium conversion have demonstrated less than a 5% difference between the two assays for determination of growth factor content of several samples.

Features and Benefits

Gain Sensitivity: Detect as few as 1,000 cells/well with a 96-well plate reader. Greater sensitivity than the neutral red assay procedure.

Use With a Variety of Cells: Assay mammalian, plant and yeast cells.

Non-Radioactive: Requires no scintillation cocktail or radioactive waste disposal.

Save Time: Perform the assay in a 96-well plate with no washing steps, no cell harvesting and no scintillation counting.

Convenient and Adapts to Your Needs: Requires no weighing or mixing of dye compounds and follows either a 4-hour or overnight protocol.


Specifications

Catalog Number:

Contenido

Item Part # Presentación

Solubilization Solution/Stop Mix

G401A 1 × 100ml

Dye Solution

G402A 1 × 15ml

Certificado de Análisis

Search by lot number

Use Restrictions

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

Condiciones de Almacenaje

Store Dye Solution at –20°C and Solubilization/Stop Solution at room temperature.

Contenido

Item Part # Presentación

Solubilization Solution/Stop Mix

G4101 1 × 500ml

Dye Solution

G4102 1 × 75ml

Certificado de Análisis

Search by lot number

Use Restrictions

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

Condiciones de Almacenaje

Store Dye Solution at –20°C and Solubilization/Stop Solution at room temperature.

Resources

No related resources available