Pierce™ Gaussia Luciferase Glow Assay Kit
Pierce™ Gaussia Luciferase Glow Assay Kit
Thermo Scientific™

Pierce™ Gaussia Luciferase Glow Assay Kit

The Thermo Scientific Pierce Gaussia Luciferase Glow Assay Kit provides a sensitive bioluminescence system to determine expression of a geneRead more
Have Questions?
Change viewbuttonViewtableView
Catalog NumberQuantity
16160100 Reactions
161611000 Reactions
Catalog number 16160
Price (USD)
133.00
Each
Add to cart
Quantity:
100 Reactions
Price (USD)
133.00
Each
Add to cart

The Thermo Scientific Pierce Gaussia Luciferase Glow Assay Kit provides a sensitive bioluminescence system to determine expression of a gene of interest with a luciferase reporter. The extremely bright and stable bioluminescence signal (half-life greater than 1 hour) is produced in the presence of the Gaussia-Dura luciferase reporter due to oxidation of the luciferase substrate coelenterazine (Figure 1). Gaussia luciferase is a 20 kDa protein from the marine copepod, Gaussia princeps, that has greater protein stability and signal brightness than firefly and native Renilla luciferase. The bioluminescent enzyme is highly secreted into the cell culture media, allowing for live cell monitoring of reporter activity. Light output generated by the luciferase reaction can be correlated to the amount of Gaussia luciferase protein produced and used to determine the activity of the promoter driving Gaussia expression.

Features of the Gaussia Luciferase Glow Assay Kit:
Sensitive—highly sensitive detection of Gaussia luciferase activity
Stable—increased signal stability
Simple—does not require a luminometer with injectors
Compatible—assay reagents compatible with other Gaussia luciferases
Automation-friendly—amenable to high throughput assays
Convenient—contains a universal cell lysis buffer and optimized glow assay reagent
Safe—allows one to perform non-radioactive assays

When used with Thermo Scientific Gaussia-Dura Luc Vectors, the kit provides an extremely sensitive bioluminescent reporter assay system for detection of secreted or intracellular luciferase activity from promoter or pathway activation with extended signal stability. The light output generated by the luciferase reaction (emission maximum of 485 nm) indicates that Gaussia luciferase was transcribed. This light emission can be correlated to the amount of luciferase protein produced, which in turn is proportional to the activity of the promoter for Gaussia luciferase expression and indicates that the regulatory region of the target gene was active. This reaction does not require adenosine triphosphate (ATP) or other cofactors. The kit includes cell lysis buffer, reaction buffer and substrate and can be used to detect the activity of any Gaussia luciferases or derivatives that use coelenterazine as a substrate.

The Gaussia Luciferase Glow Assay Kit requires:
Gaussia luciferase and luminometer or other instrument capable of monitoring luminescence, such as Thermo Scientific Varioskan LUX Microplate Readers.

Applications of the Gaussia Luciferase Glow Assay Kit:
• Promoter studies for analyzing cis- regulatory elements and trans-acting factors
• Drug screening
• siRNA and miRNA screening
• Multiplexed assays to study off-target effects
• Secretory pathway/protein localization reporter assays
• Signal transduction pathway analysis
• RNA splicing studies

The Gaussia-Dura gene used in the Thermo Scientific Gaussia-Dura Luc Vectors is derived from the wild type Gaussia gene and provides equally bright but more stable light output. The Gaussia Glow Assay Kit reagent yields a Gaussia-Dura luciferase reaction with glow-type kinetics that provides a lower intensity but longer-duration signal allowing for higher sample throughput. This glow-type assay with a prolonged luminescence signal does not require reagent injectors and is recommended for luminometers without injectors or for applications requiring batch processing of samples.

WARNING: Reproductive Harm - www.P65Warnings.ca.gov
For Research Use Only. Not for use in diagnostic procedures.
Specifications
TypeAssay Kit
TargetLuciferase, Gaussia Luciferase
Sufficient For100 Luciferase Assays
Quantity100 Reactions
AssayReporter Enzyme, Luciferase Reporter Assay
Compatible CellsMammalian Cells
Detection MethodBioluminescence
For Use With (Equipment)Luminometer (Microplate)
Format384-well plate, 96-well plate
Label TypeEnzyme Labeled
Substrate PropertiesChemical Substrate
TechniqueEnhanced Chemiluminescence
Substrate TypeLuciferase Substrate
Product LinePierce™
SubstrateCoelenterazine
PromoterEF-1α
Unit SizeEach
Contents & Storage
Sufficient For: 100 luciferase assays in microplate wells
• Gaussia Glow Assay Buffer, 5 mL (store at 4°C)
• 100X Coelenterazine, 50 μL (store at -80°C)
• Luciferase Cell Lysis Buffer (2X), 6 mL (store at room temperature)

Kit may be stored at -80°C, or individually at indicated temperatures.

Frequently asked questions (FAQs)

I got a high background signal with a Gaussia/Cypridina/Renilla Luciferase Glow/Luciferase Flash assay. What went wrong?

Here are possible causes and solutions:

- Non-specific oxidation of substrate: Use less serum in the cell culture media; Note: Albumin can increase the auto-oxidation of Vargulin; Avoid repeated freezing and thawing of the sample.
- Control sample is contaminated: Use new sample; Change pipette tips after each well.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

I am getting a high saturating signal with a Gaussia/Cypridina/Renilla Luciferase Glow/Luciferase Flash assay. What could have happened?

This could be due to high luciferase expression. Here are some suggestions:

  • Reduce incubation time before collecting samples. 
  • Decrease the integration time on the instrument.
  • Dilute the sample: for secreted Gaussia/Cypridina Luciferase, dilute the sample using media from the cell culture; for cell lysate, dilute the sample using lysis buffer 


  • Note: A low sample volume can increase assay variability. Dilute the sample and use the recommended volume of 10-20 µL per assay.

    Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

    Why am I getting a low signal in lysate using a Gaussia/Cypridina/Renilla Luciferase Glow/Luciferase Flash assay? Can you provide some suggestions?

    Here are possible causes and solutions:

    - Non-optimized lysis buffer used: Assay luciferase activity in the media to confirm good expression of luciferase; Use only the provided lysis buffer.
    - Low luciferase expression: Lyse cells in smaller volume of 1X Cell Lysis Buffer; Use a different promoter or growth conditions to improve expression; Increase the integration time on the instrument; Scale up volume of sample and reagent per well.

    Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

    I got a low signal in media when I used a Gaussia/Cypridina/Renilla Luciferase Glow/Luciferase Flash assay. What happened?

    Here are possible causes and solutions:

    - Insufficient luciferase accumulation in media: Incubate cells for a longer time.
    - Low luciferase expression: Use less media per well during the experiment;.Use a different promoter or growth conditions to improve expression;.Increase the integration time on the instrument;.Scale-up the volume of sample and reagent per well.
    - Treatment interfered with cellular secretory pathway: Transfect cells with a plasmid for constitutive expression of Luciferase (i.e., with pTK or pCMV promoter); Determine if luciferase actively expresses in media without treatment. Add treatment; Determine if there is a corresponding drop in luciferase activity from the constitutively expressed plasmid.

    Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

    I am getting no signal with my Gaussia/Cypridina/Renilla Luciferase Glow/Luciferase Flash assay. Why is this?

    Here are possible causes and solutions:

    - Low transfection efficiency: Optimize transfection conditions using a visual transfection control (e.g., a plasmid over-expressing a fluorescent protein); Verify plasmid DNA quality - use only transfection grade DNA; Use actively dividing, low passage cells; Use a different cell type.
    - No or low promoter activity: Use conditions known for promoter activation; Incubate cells for a longer time; Change growth conditions to improve expression; Use a different promoter.
    - Substrate auto-oxidized: Protect substrate from light and air; Maintain 100X Coelenterazine at -80 degrees C; maintain 100X Vargulin at -80 degrees C; Prepare new Coelenterazine Working Solution if used longer than 8 hours; Prepare new Vargulin Working Solution if used longer than 2 hours

    Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.