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.

G8941_Viral-ToxGlo--Assay--10ml_3 G8942_Viral-ToxGlo--Assay--10-x-10ml_3 G8943_Viral-ToxGlo--Assay--100ml_3

Determine Viral CPE or Monitor Compounds for Antiviral Activity

  • Easy, simple protocol measures ATP
  • Quantifiable assay for measuring viral-induced cytopathic effect (CPE)
  • Compatible with high-throughput screening

Catalog Number:

Size

Catalog Number: G8941

Consultar Precio

Catalog Number: G8942

Consultar Precio

Catalog Number: G8943

Consultar Precio


Overview
Protocols
Specifications
Resources
Related Products

The Viral ToxGlo™ Assay is a simple, quantifiable method of determining viral-induced cytopathic effects (CPE) in host cells caused by lytic virions. The assay measures cellular ATP as a surrogate measure of host cell viability. When CPE occurs due to viral infection, ATP depletion can be measured and correlated with viral burden. The amount of ATP detected is directly proportional to the number of viable host cells in culture and can be used as a simple method to quantify viral-induced CPE. The homogeneous "add-mix-measure" assay procedure involves adding the single reagent (ATP Detection Reagent) directly to host cells following viral treatment. A “glow-type” luminescent signal is generated that is proportional to the amount of ATP present. Cell washing, multiple pipetting steps and visual assessment are not required to assess CPE. The system detects as few as 15 cells/well in a 384-well format in 10 minutes after reagent addition and mixing and is designed for use in multiwell formats, making it ideal for automated high-throughput screening (HTS).

Features and Benefits

Objectively Quantify CPE: The assay provides quantifiable data by luminescence detection, which obviates subjective operator error associated with visual scoring methods.

Decrease Time to Results: Data can be recorded and analysis begun 10 minutes after reagent addition.

Simplify Assessment of CPE: The homogeneous “add-mix-measure” protocol dramatically reduces the manual steps required for CPE assessment.

Choose Your Format: The reagent is scalable from 96- to 1536-well plate formats.

Amenable to High-Throughput Screening: Luminescent signal is very stable with a half-life generally >5 hours dependent on cell type and medium used, allowing batch or consecutive processing. No fluorescence interference results in high signal to background and delivers excellent Z′ values in screening applications.

Applications include the determination of viral infectivity and the corresponding tissue culture infective dose (TCID50) and potential antiviral potency or off-target toxicity of test compounds.

 

This method is only useful for viruses that produce cytotoxicity and CPE.


Quantifiable Measure of CPE

11321MB_936px

Increased luminescence indicates less infective virus and less CPE. Panel A. Dilutions of Influenza virus H1N1 were applied to MDCK monolayers. Panel B. Dilutions of VEEV applied to Vero E6 monolayers. Panel C. Dilutions of dengue virus applied to BHK-21 monolayers. Panel D. Dilutions of RSV applied to A549 monolayers. After incubation, ATP Detection Reagent was added directly to cells and luminescence measured.


Accurately Calculate Toxicity of Test Compounds

Fast and simple determination of antiviral potency.

Panel A. Test compound reduces viral CPE with no off-target cytotoxicity. MDCK cells with 100 TCID50 of H1N1 (on-target antiviral) or MDCK cells only (off-target cytotoxicity). Panel B. Test compound reduces viral CPE and also causes off-target cytotoxicity. BHK-21 cell monolayer with 100 TCID50 of Dengue virus (on-target antiviral) or BHK-1 cells only (off-target cytotoxicity). After incubation, ATP Detection Reagent was added directly to cells and luminescence measured.

Specifications

Catalog Number:

Contenido

Item Part # Presentación

ATP Detection Buffer

G806A 1 × 10ml

ATP Detection Substrate

V363A 1 × 1 vial

Certificado de Análisis

Search by lot number

Use Restrictions

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

Condiciones de Almacenaje

BB

Contenido

Item Part # Presentación

ATP Detection Buffer

G806A 10 × 10ml

ATP Detection Substrate

V363A 10 × 1 vial

Certificado de Análisis

Search by lot number

Use Restrictions

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

Condiciones de Almacenaje

BB

Contenido

Item Part # Presentación

ATP Detection Buffer

G806B 1 × 100ml

ATP Detection Substrate

V363B 1 × 1 vial

Certificado de Análisis

Search by lot number

Use Restrictions

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

Condiciones de Almacenaje

BB

Resources

Otros