Dual-Glo® Luciferase Assay System
Detects firefly and <i>Renilla</i> Luciferase Activities in a Single Sample
- Renilla luciferase internal control provides more accurate results
- Assay cells directly in growth medium for both reporters
- Extended half-life of 2 hours for each reporter
Catalog Number:
Size
Catalog Number: E2920
Catalog Number: E2940
Catalog Number: E2980
An Extended-Life Dual-Luciferase Assay with "Add-Mix-Measure" Convenience
The Dual-Glo® Luciferase Assay System is a homogeneous reagent system that enables fast and simple quantitation of a stable luminescent signal from two reporter genes in a single sample. The convenient "add-mix-measure" protocol generates both firefly and Renilla luciferase luminescence signals from cells that have not been preconditioned or prelysed.
With the Dual-Glo® System, internal controls can be established to minimize sample variability by reducing false-positive and false-negative readings caused by nonspecific factors such as cytotoxicity. In the Dual-Glo® Luciferase Assay, the activity of the primary reporter is correlated with the effect of specific stimuli, and the activity of the co-transfected control reporter provides an internal control to normalize results.
The system is optimized for batch processing both 96- and 384-well plates and is compatible with a wide variety of mammalian cell culture media. The Dual-Glo® Luciferase Assay System provides high Z´-factors for cell-based, high-throughput screening applications.
Assay Advantages
- Increased Precision and Accuracy. Assay normalization using an internal control co-reporter minimizes the effects of variations in cell number and health, transfection efficiency and nonspecific cellular responses.
- No centrifugation or pre-lysis steps required. Reagents are added directly to growth medium for both reporters.
- Stable signal allows flexibility for batch or continuous processing of 96- and 384-well plates. Each luminescent signal can be measured for up to 2 hours after reagent addition.
- Simple, two-step assay is compatible with any luminometer. On-board injectors not required.
- Wide Dynamic Range allows analysis of high and low reporter activity without sample dilution. Linear over at least 6 logs of enzyme concentration for each reporter.
Learn more about custom options for this product at:Â www.promega.com/custom/Â
Contact Promega for information on bulk purchases.
Protocols
Complete Protocol
Quick Protocols
Specifications
Catalog Number:
What's in the box?
| Item | Part # | Size |
|---|---|---|
|
Dual-Glo® Luciferase Substrate |
E297A | 1 × 1 vial |
|
Dual-Glo® Luciferase Buffer |
E298A | 1 × 10ml |
|
Dual-Glo® Stop & Glo® Substrate |
E313A | 1 × 100μl |
|
Dual-Glo® Stop & Glo® Buffer |
E314A | 1 × 10ml |
SDS
Search for SDSCertificate of Analysis
Use Restrictions
For Research Use Only. Not for Use in Diagnostic Procedures.Storage Conditions
See Protocol for detailed storage recommendations.
What's in the box?
| Item | Part # | Size |
|---|---|---|
|
Dual-Glo® Luciferase Substrate |
E297B | 1 × 1 vial |
|
Dual-Glo® Luciferase Buffer |
E298B | 1 × 100ml |
|
Dual-Glo® Stop & Glo® Substrate |
E313B | 1 × 1,000μl |
|
Dual-Glo® Stop & Glo® Buffer |
E314B | 1 × 100ml |
SDS
Search for SDSCertificate of Analysis
Use Restrictions
For Research Use Only. Not for Use in Diagnostic Procedures.Storage Conditions
See Protocol for detailed storage recommendations.
What's in the box?
| Item | Part # | Size |
|---|---|---|
|
Dual-Glo® Luciferase Substrate |
E297B | 10 × 1 vial |
|
Dual-Glo® Luciferase Buffer |
E298B | 10 × 100ml |
|
Dual-Glo® Stop & Glo® Substrate |
E313B | 10 × 1,000μl |
|
Dual-Glo® Stop & Glo® Buffer |
E314B | 10 × 100ml |
SDS
Search for SDSCertificate of Analysis
Use Restrictions
For Research Use Only. Not for Use in Diagnostic Procedures.Storage Conditions
See Protocol for detailed storage recommendations.
Resources
Articles
- m6A methylation orchestrates IMP1 regulation of microtubules during human neuronal differentiation
- Delivery of a BET protein degrader via a CEACAM6-targeted antibody–drug conjugate inhibits tumour growth in pancreatic cancer models
- This study sought to the effect of branched chemically modified poly(A) tails on enhancing mRNA stability and translation capacity.
- Optimize shRNA Target Sites Using Bioluminescent Reporters
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