TaqMan™ Fast Advanced Master Mix for qPCR
Pair your qPCR Master Mix with ready to use TaqMan Gene Expression, Genotyping Assay or Custom Probes for multiplexing. Use our helpful TaqMan Search Wizard to find the Assays for your target of interest. Learn more
TaqMan™ Fast Advanced Master Mix for qPCR
Applied Biosystems™

TaqMan™ Fast Advanced Master Mix for qPCR

TaqMan Fast Advanced Master Mix delivers accurate quantification and dependability in less time on an array of qPCR instrument platforms.
Catalog NumberQuantity
44445561 x 1 mL
44445571 x 5 mL
44449632 x 5 mL
44449645 x 5 mL
444496510 x 5 mL
44445581 x 50 mL
Catalog number 4444556
Price (JPY)
18,300
Each
Contact Us ›
Quantity:
1 x 1 mL

TaqMan Fast Advanced Master Mix delivers accurate quantification and dependability in less time on an array of qPCR instrument platforms. It provides best in class performance, including the widest quantifiable range, in both single and duplex reactions, even with challenging targets. TaqMan Fast Advanced Master Mix contains AmpliTaq Fast DNA Polymerase, uracil-N-glycosylase (UNG), dNTPs with dUTP, ROX dye (passive reference), and optimized buffer components. It is supplied at a 2X concentration.

Features of the TaqMan Fast Advanced Master Mix include:

  • Best-in-class performance—superior sensitivity, accuracy, dynamic range, and specificity compared to standard mixes in standard mode
  • Engineered for enhanced benchtop stability—stable at room temperature for up to 72 hours in preassembled reactions
  • Optimized for multiplexing—validated for duplexing with exogenous and endogenous internal positive control assays
  • Reduced run times (<40 minutes) on fast and standard instrumentation—optimized for fast mode on fast instruments and fast cycling conditions on standard instruments
  • Seamlessly transitions into your experiments—validated with TaqMan assays for gene expression and microRNAs, and TaqMan array micro-fluidic cards

Best-in-class performance

TaqMan Fast Advanced Master Mix has been designed to provide performance equal to or better than standard master mixes. It has been benchmarked against the leading suppliers' standard and fast master mixes to help ensure that it succeeds in providing best-in-class sensitivity, accuracy, dynamic range, and specificity. TaqMan Fast Advanced Master Mix's dynamic range (up to 7 logs) is the widest in the industry. The impressive sensitivity of the mix is showcased in the figure below which compares the Ct values of TaqMan Fast Advanced Master Mix and TaqMan Universal PCR Master Mix across a panel of gene expression assays.

Benchtop stability for high-throughput handling and convenience

TaqMan Fast Advanced Master Mix has been engineered to retain a high level of performance in preassembled reactions for up to 72 hours. The stability of this mix provides users of high-throughput liquid handling systems the assurance that the results on the first plate will mimic those of the last plate. The figure below shows an assay that was run upon assembly (time 0) and after 72 hours of incubation at 30°C, simulating the most extreme room temperature scenario.

For those with less extreme throughput needs, the enhanced stability of this master mix provides an overall added convenience to your workflow, as you are no longer constrained to immediately running plates upon assembly.

Optimized for multiplexing

We realize that confidence is paramount when it comes to your results. For added confidence in the results in every well, TaqMan Fast Advanced Master Mix has been designed to help deliver accurate results for duplex reactions using an internal positive control (IPC). The figure below shows results for the experimental target β-actin (gene name: ACTB), which was serially diluted and amplified in single-target reactions and duplex reactions.

Validated for microRNA assays

TaqMan Fast Advanced Master Mix has been validated for use with multiple real-time PCR applications, including microRNA assays. The formulation provides high specificity and dynamic range, the two most critical performance attributes that define successful results when working with microRNAs. The data in the figure below demonstrate excellent PCR linearity over a 6-log range of input template.

Reduced run times on standard instrumentation

TaqMan Fast Advanced Master Mix has been optimized for use with both fast and standard instrumentation, enabling researchers who currently own standard instruments to also reap the performance benefits and time savings this mix provides. The figure below showcases the impressive results achieved when using TaqMan Fast Advanced Master Mix under fast thermal cycling conditions on the Applied Biosystems 7300 Real-Time PCR System. The mix has been tested with all Applied Biosystems standard real-time PCR instrumentation (7900HT, 7500, and 7300 systems) to enable success independent of whether or not you own a fast-enabled instrument.

For Research Use Only. Not for use in diagnostic procedures.
Specifications
Fidelity (vs. Taq)2 X
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 Flex, QuantStudio 7 Pro, StepOne, StepOnePlus, ViiA 7 System
IncludesdUTP, UNG/UDG
Inhibitor Tolerance (Simple)High
Multiplex CapabilityDuplex
No. of Reactions100 Reactions
Passive Reference DyeROX (Pre-mixed)
PolymeraseAmpliTaq Fast DNA Polymerase
Product LineTaqMan
Product TypeFast Advanced Master Mix
Quantity1 x 1 mL
Sample TypeDNA (Genomic), cDNA
Shipping ConditionWet Ice
Target SpecificitycDNA or gDNA only
Thermostability72 hr., Assembled Reaction
Volume1 mL
Concentration2X
Detection MethodPrimer-probe
For Use With (Application)Gene Expression, DNA Quantitation, Presence/Absence, miRNA analysis
FormLiquid
GC-Rich PCR PerformanceHigh
PCR MethodqPCR
Reaction SpeedFast
Unit SizeEach
Contents & Storage
Contains 1 tube (1 mL) 2X TaqMan Fast Advanced Master Mix sufficient for 100 reactions

TaqMan Fast Advanced Master Mix contains AmpliTaq Fast DNA Polymerase, Uracil-N glycosylase (UNG), dNTPs (with dUTP), ROX dye (passive reference), and optimized buffer.

Store at 2°C to 8°C in the dark.

Frequently asked questions (FAQs)

What can I do to improve the sensitivity of my qPCR assay?

If you are targeting a low-abundance gene, you may have trouble getting Ct values in a good, reliable range (Ct > 32). To increase the sensitivity of the assay, you may want to consider the following:

- Increase the amount of RNA input into your reverse transcription reaction, if possible
- Increase the amount of cDNA in your qPCR reaction (20% by volume max)
- Try a different reverse transcription kit, such as our SuperScript VILO Master Mix, for the highest cDNA yield possible
- Consider trying a one-step or Cells-to-CT type workflow (depending on your sample type)

How do I set the baseline for my qPCR experiment?

Most times your instrument software can automatically set a proper baseline for your data. Check out our short video, Understanding Baselines, for more information on how to set them (https://www.youtube.com/watch?feature=player_embedded&v=5BjFAJHW-bE).

How do I set the threshold for my qPCR experiment?

In most cases your instrument software can automatically set a proper threshold for your data. Check out our short video, Understanding Thresholds, for more information on how to set them (https://www.youtube.com/watch?feature=player_embedded&v=H_xsuRQIM9M).

I am not getting any amplification with my TaqMan Assay or SYBR Green primer set. What is causing this?

There could be several reasons for no amplification from an assay or primer set. Please see these examples and suggested solutions in our Real-Time Troubleshooting Tool (https://www.thermofisher.com/us/en/home/life-science/pcr/real-time-pcr/qpcr-education/real-time-pcr-troubleshooting-tool/gene-expression-quantitation-troubleshooting/no-amplification.html) for more details.

I am getting amplification in my no-template control (NTC) wells in my qPCR experiment. What is causing this?

There could be several reasons for amplification in a NTC well. Please see these examples and suggested solutions in our Real-Time Troubleshooting Tool (https://www.thermofisher.com/us/en/home/life-science/pcr/real-time-pcr/qpcr-education/real-time-pcr-troubleshooting-tool/gene-expression-quantitation-troubleshooting/amplification-no-template-control.html) for more details.

Citations & References (3430)

Citations & References
Abstract
Microglia TREM2(R47H) Alzheimer-linked variant enhances excitatory transmission and reduces LTP via increased TNF-α levels.
Authors:Ren S,Yao W,Tambini MD,Yin T,Norris KA,D'Adamio L
Journal:eLife
PubMed ID:32579116
To study the mechanisms by which the p.R47H variant of the microglia gene and Alzheimer’s disease (AD) risk factor TREM2 increases dementia risk, we created Trem2(R47H) KI rats. Trem2(R47H) rats were engineered to produce human Aβ to define human-Aβ-dependent and -independent pathogenic mechanisms triggered by this variant. Interestingly, pre- and ... More
PARP9-DTX3L ubiquitin ligase targets host histone H2BJ and viral 3C protease to enhance interferon signaling and control viral infection.
Authors:Zhang Y,Mao D,Roswit WT,Jin X,Patel AC,Patel DA,Agapov E,Wang Z,Tidwell RM,Atkinson JJ,Huang G,McCarthy R,Yu J,Yun NE,Paessler S,Lawson TG,Omattage NS,Brett TJ,Holtzman MJ
Journal:Nature immunology
PubMed ID:26479788
Enhancing the response to interferon could offer an immunological advantage to the host. In support of this concept, we used a modified form of the transcription factor STAT1 to achieve hyper-responsiveness to interferon without toxicity and markedly improve antiviral function in transgenic mice and transduced human cells. We found that ... More
Unique maternal immune and functional microbial profiles during prenatal stress.
Authors:Antonson AM,Evans MV,Galley JD,Chen HJ,Rajasekera TA,Lammers SM,Hale VL,Bailey MT,Gur TL
Journal:Scientific reports
PubMed ID:33219314
Maternal stress during pregnancy is widespread and is associated with poor offspring outcomes, including long-term mental health issues. Prenatal stress-induced fetal neuroinflammation is thought to underlie aberrant neurodevelopment and to derive from a disruption in intrauterine immune homeostasis, though the exact origins are incompletely defined. We aimed to identify divergent ... More
A puromycin selectable cell line for the enrichment of mouse embryonic stem cell-derived V3 interneurons.
Authors:Xu H,Iyer N,Huettner JE,Sakiyama-Elbert SE
Journal:Stem cell research & therapy
PubMed ID:26555777
INTRODUCTION: Spinal V3 interneurons (INs) are a commissural, glutamatergic, propriospinal neuron population that holds great potential for understanding locomotion circuitry and local rewiring after spinal cord injury. Embryonic stem cells hold promise as a cell source. However, the inevitable heterogeneity resulting from differentiation protocols makes studying post-mitotic stem cell-derived neuron ... More
Electrospun biomaterial scaffolds with varied topographies for neuronal differentiation of human-induced pluripotent stem cells.
Authors:Mohtaram NK,Ko J,King C,Sun L,Muller N,Jun MB,Willerth SM
Journal:Journal of biomedical materials research. Part A
PubMed ID:25524598