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PowerUp™ SYBR™ Green Master Mix for qPCR
PowerUp™ SYBR™ Green Master Mix for qPCR
PowerUp™ SYBR™ Green Master Mix for qPCR
PowerUp™ SYBR™ Green Master Mix for qPCR
Applied Biosystems™

PowerUp™ SYBR™ Green Master Mix for qPCR

PowerUp™ SYBR™ Green Master Mix is a pre-formulated, optimized, universal 2X master mix for real-time PCR workflows. Coupled with user-suppliedRead more
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A25741Promo Image1 mL
A25742Promo Image5 mL
A25743Promo Image50 mL
A25778Promo Image10 x 5 mL
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Catalog number A25741
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1 mL
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Price (USD)
117.65
Online Exclusive
125.00
Save 7.35 (6%)
Each
Add to cart
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PowerUp™ SYBR™ Green Master Mix is a pre-formulated, optimized, universal 2X master mix for real-time PCR workflows. Coupled with user-supplied primer sets and template, PowerUp™ SYBR™ Green Master Mix is designed to amplifiy targets for accurate gene expression analysis.

PowerUp™ SYBR™ Green Master Mix features include:

  • A dual hot-start mechanism for excellent specificity
  • Highly reproducible CTs over a broad dynamic range
  • Inclusion of UDG to help prevent carryover contamination
  • Stability of pre-assembled reactions for up to 72 hours
  • Compatibility with most real-time qPCR instruments

Exceptional specificity with dual hot-start mechanism

Specificity is paramount in obtaining high-quality data in SYBR™ Green reactions and can be enhanced through control of the Taq DNA polymerase at lower temperatures before stringent primer binding. PowerUp™ SYBR™ Green Master Mix uses the Dual-Lock™ Taq DNA polymerase enzyme that combines two unique hot-start mechanisms to help control its activity and to prevent undesirable early activity of the polymerase at low temperatures. In an experiment evaluating 24 different primer sets, PowerUp™ SYBR™ Green Master Mix generated single melt curves 100% of the time, consistent with highly specific amplification.

Tight reproducibility in CTs over a wide dynamic range

PowerUp™ SYBR™ Green Master Mix demonstrates excellent reproducibility over a wide dynamic range for a variety of targets tested (see figure). In addition, this master mix provides efficient amplification over 6 logs of sample input. Unlike competitor mixes that can exhibit inhibition at high cDNA inputs and low correlation coefficients over a dynamic range experiment, PowerUp™ SYBR™ Green Master Mix efficiency is maintained over the full dynamic range to help deliver maximal confidence in data quality (see figure).

UDG included for carryover contamination control

The inclusion of uracil-DNA glycosylase (UDG) and dUTP in the PowerUp™ SYBR™ Green Master Mix enables the degradation of any previously amplified PCR products, helping prevent contamination of subsequent qPCR reactions and possible false positives.

Stability of pre-assembled reactions

The tight control of the Dual-Lock™ Taq DNA polymerase in PowerUp™ SYBR™ Green Master Mix enables reactions to be assembled up to 72 hours prior to cycling without impacting data (see figure). This consistency allows users to have confidence and flexibility in the use of PowerUP™ SYBR™ Green Master Mix across numerous workflow scenarios¹.

Broad instrument compatibility

PowerUp™ SYBR™ Green Master Mix can be used in either standard or fast cycling mode and is compatible with all Applied Biosystems™ real-time PCR instruments². It is also compatible with the Bio-Rad IQ™5 and CFX96™ / CFX384™ systems, Roche LightCycler™ LC480, and Stratagene™ MX3005P™ systems. For optimal results, recommended primer concentrations are 300–800 nM.

Learn more about PowerUp™ SYBR™ Green Master Mix

¹Pre-PCR stability is influenced not only by the master mix, but also by the target being analyzed. For maximum confidence, researchers should confirm stability profiles of their specific targets.

² For optimal performance, standard cycling using the Applied Biosystems™ 7900 system is recommended.

For Research Use Only. Not for use in diagnostic procedures.

Specifications
Concentration2X
For Use With (Equipment)7500 Fast System, 7500 System, 7900HT System, QuantStudio™ 12k Flex, QuantStudio™ 3, QuantStudio™ 5, QuantStudio™ 6 Flex, QuantStudio 6 Pro, QuantStudio 7 Pro, QuantStudio™ 7 Flex, QuantStudio™ Absolute Q Digital PCR System, StepOne™, StepOnePlus™, ViiA™ 7 System
FormatTube
No. of Reactions100 Reactions
PolymeraseDual-Lock Taq DNA Polymerase
Product LinePowerUP™, SYBR™
Product TypeReal Time PCR SYBR Master Mix
Quantity1 mL
Sample TypeDNA
Shipping ConditionWet Ice
Sufficient For100 Reactions of 20 μL
Volume1 mL
Detection MethodSYBR
For Use With (Application)Gene Expression
PCR MethodqPCR
Reaction SpeedFast or Standard
Unit SizeEach
Contents & Storage
The 2X mix contains SYBR Green dye, Dual-Lock Taq DNA Polymerase, dNTPs with dUTP/dTTP blend, heat-labile UDG, ROX passive reference dye, and optimized buffer components. Contains 1 x 1 mL tube, sufficient for 100 20-μL reactions (10 μL Master Mix per reaction).

Store at 2–8°C in the dark.
HIghCap

For optimal RT-qPCR results

Use High-Capacity cDNA Synthesis Kits 

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Lot #Certificate TypeDateCatalog Number(s)
3266967Certificate of AnalysisJun 26, 2025A25742
3251791Certificate of AnalysisJun 25, 2025A25743
3255666Certificate of AnalysisJun 12, 2025A25741
3254235Certificate of AnalysisJun 09, 2025A25742
3240910Certificate of AnalysisMay 29, 2025A25743
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Safety Data Sheets

Frequently asked questions (FAQs)

It could be due to the following reasons:

  • Insufficient cDNA template is present. Use 10 to 100 ng of cDNA template per 50 µL reaction.
  • Quality of cDNA template is poor. Quantify the amount of cDNA template and test the cDNA template for the presence of PCR inhibitors.
  • Sample degradation. Prepare fresh cDNA, then repeat the experiment.
  • Reduced number of PCR cycles in the thermal cycling protocol. Increase the number of PCR cycles to the default setting of 40.
  • Primer-dimer formation and residual polymerase activity. Prepare the reaction mixes and reaction plate on ice. To ensure optimal results, run the reaction plate as soon as possible after completing the reaction setup.


Find additional tips, troubleshooting help, and resources within our Real-Time PCR and Digital PCR Applications Support Center.

This could be due to the following reasons:

  • Pure dye component’s spectra are incorrect. Rerun pure dye spectra.
  • Incorrect dye components have been chosen. Choose correct dyes for data analysis.


Find additional tips, troubleshooting help, and resources within our Real-Time PCR and Digital PCR Applications Support Center.

We recommend using the High-Capacity RNA-to-cDNA Kit (Cat. No. 4387406, 4388950).

Find additional tips, troubleshooting help, and resources within our Real-Time PCR and Digital PCR Applications Support Center.

The recommended primer concentration range is 300-800 nM. You will need to optimize the primer concentration by running different concentration combinations of the forward and reverse primer. See page 28 of the PowerUp SYBR Green Master Mix User Guide.

Find additional tips, troubleshooting help, and resources within our Real-Time PCR and Digital PCR Applications Support Center.

This master mix has a heat-labile UDG. It is completely and irreversibly inactivated after 10 minute incubation at 50°C.

Find additional tips, troubleshooting help, and resources within our Real-Time PCR and Digital PCR Applications Support Center.

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