TaqMan™ Fast Virus 1-Step Master Mix for qPCR
TaqMan™ Fast Virus 1-Step Master Mix for qPCR
TaqMan™ Fast Virus 1-Step Master Mix for qPCR
TaqMan™ Fast Virus 1-Step Master Mix for qPCR
Applied Biosystems™

TaqMan™ Fast Virus 1-Step Master Mix for qPCR

TaqMan Fast Virus 1-Step Master Mix is designed for fast, highly sensitive real-time RT-PCR, even in the presence of challenging PCR inhibitors.
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Número do catálogoQuantity
44444345 x 1 mL
44444361 x 10 mL
44444321 x 1 mL
Número do catálogo 4444434
Preço (BRL)
6.298,50
Each
Adicionar ao carrinho
Quantity:
5 x 1 mL
Preço (BRL)
6.298,50
Each
Adicionar ao carrinho

The features of the kit have been selected to enhance virus detection on commonly used sample types. A single-tube format allows for uniform handling and processing for both RNA and DNA viruses.

TaqMan Fast Virus 1-Step Master Mix is designed for fast, highly sensitive real-time RT-PCR even in the presence of challenging PCR inhibitors. The 4X formulation provides enhanced detection of both RNA and DNA viruses and is ideal for multiplex gene expression studies, even with low target input. The TaqMan Fast Virus 1-Step Master Mix provides a single-tube format for uniform handling and processing, while delivering qPCR cycling in less than 30 minutes, helpful when working in high throughput workflows.

Key product features:

  • High sensitivity—4X master mix to amplify both RNA and DNA with improved sensitivity
  • Consistent results—formulated to handle common RT-PCR inhibitors found in blood, stool, and other difficult samples
  • Simplified application— one-tube, one-step master mix, offering a single run profile with RNA and DNA, which allows for easy mix-and-match of targets on a plate
  • Target flexibility—works in singleplex, multiplex, and with exogenous or endogenous internal controls
  • High efficiency—increased qRT-PCR speed on fast and on standard instruments

Two formulations

The master mix is available in two formulations:

  • TaqMan Fast Virus 1-Step Master Mix containing ROX dye as a passive reference is recommended for singleplex (1 probe) and up to triplex (3 probes) reactions
  • TaqMan Fast Virus 1-Step Multiplex Master Mix (No ROX) (Cat. No. 5555532), which does not contain a passive reference, is recommended for use with assays utilizing the JUN (or similar omission wavelength) dye or for higher order multiplexing (>3 targets)

High sensitivity

Many common research samples with viral nucleic acids have very low levels of target. We have optimized the master mix for high-sensitivity detection of viral targets. The higher-concentration master mix allows you to set up smaller reactions, which means that you can perform fast cycling protocols and obtain at least the same sensitivity as is expected from standard-cycling qPCR. Alternatively, larger sample input amounts can be added to standard reaction volumes for more accurate quantification of low-titer samples (figure below).

Consistent results in the presence of inhibitors

Research samples commonly assayed for viruses include blood, dirt, and tissues. Buffer components and proprietary additives in the TaqMan Fast Virus 1-Step Master Mix have been optimized to handle RT-PCR inhibitors (figure below) to help ensure consistent performance even with these difficult samples, so that you can be more confident in your results.

Flexibility in targets

It is common for labs to test for both RNA and DNA viruses in a variety of samples. To simplify your experiments, a single TaqMan Fast Virus 1-Step Master Mix protocol has been developed to assay both types of nucleic acid, so you can perform RNA and DNA virus queries next to each other on the same plate using the same handling steps (figure below). Additionally, because virus research often includes multiplexed primers and probes and internal reaction controls, we have optimized the master mix to work with multiple target amplicons (figure below).

Fast results

The TaqMan Fast Virus 1-Step Master Mix speeds your time to results and maximizes the use of your real-time PCR instruments with a fast protocol. The high-concentration formulation allows for more target nucleic acid sample to be added in the smaller reaction volumes required to run fast protocols. This enables you to maintain sensitivity with low-titer research samples while improving speed and throughput (figure below).

TaqMan Fast Virus 1-Step Master Mix provides a reliable and efficient reagent for real-time RT-PCR of virus samples that does not sacrifice accuracy. Its robust performance in the presence of common RT-PCR inhibitors and its convenient and flexible reaction setup allows you to have more confidence in your results.

For Research Use Only. Not for use in diagnostic procedures.
Especificações
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, StepOne, StepOnePlus, ViiA 7 System
FormatTube
Hot StartBuilt-In Hot Start
Inhibitor Tolerance (Simple)High
Multiplex CapabilityUp to 3-plex
No. of Reactions1000 Reactions
Passive Reference DyeROX (Pre-mixed)
PolymeraseAmpliTaq Fast DNA Polymerase
Product LineTaqMan
Product Type1-Step Master Mix
Quantity5 x 1 mL
Reverse TranscriptaseM-MLV
Sample TypeTotal RNA, Viral DNA, Viral RNA, mRNA
Shipping ConditionDry Ice
Sufficient For1000 Reactions
Target SpecificityRNA only, Both RNA and DNA
ThermostabilityNot Applicable
Detection MethodPrimer-probe
For Use With (Application)Microbial Detection, Gene Expression, DNA Quantitation, Presence/Absence
FormLiquid
PCR Method1-step RT-qPCR
Reaction SpeedFast or Standard
Unit SizeEach
Conteúdo e armazenamento
Contains 5 x 1 mL tubes of 4X RT-PCR master mix sufficient for 1000 x 20 μL reactions. Components of each:
• AmpliTaq™ Fast DNA Polymerase, UP
• Thermostable MMLV Reverse Transcriptase
• dNTPs
• RNase Inhibitor (RNaseOUT™)
• ROX™ dye (passive reference)

Store at -15°C to -25°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.

Citações e referências (959)

Citações e referências
Abstract
Diagnosing the novel SARS-CoV-2 by quantitative RT-PCR: variations and opportunities.
Authors:Barreto HG,de Pádua Milagres FA,de Araújo GC,Daúde MM,Benedito VA
Journal:Journal of molecular medicine (Berlin, Germany)
PubMed ID:33067676
The world is currently facing a novel viral pandemic (SARS-CoV-2), and large-scale testing is central to decision-making for the design of effective policies and control strategies to minimize its impact on the global population. However, testing for the presence of the virus is a major bottleneck in tracking the spreading ... More
DNA vaccination protects mice against Zika virus-induced damage to the testes.
Authors:Griffin BD,Muthumani K,Warner BM,Majer A,Hagan M,Audet J,Stein DR,Ranadheera C,Racine T,De La Vega MA,Piret J,Kucas S,Tran KN,Frost KL,De Graff C,Soule G,Scharikow L,Scott J,McTavish G,Smid V,Park YK,Maslow JN,Sardesai NY,Kim JJ,Yao XJ,Bello A,Lindsay R,Boivin G,Booth SA,Kobasa D,Embury-Hyatt C,Safronetz D,Weiner DB,Kobinger GP
Journal:Nature communications
PubMed ID:28589934
Zika virus (ZIKV) is an emerging pathogen causally associated with serious sequelae in fetuses, inducing fetal microcephaly and other neurodevelopment defects. ZIKV is primarily transmitted by mosquitoes, but can persist in human semen and sperm, and sexual transmission has been documented. Moreover, exposure of type-I interferon knockout mice to ZIKV ... More
Inhibitory effect of lactoferrin-coated zinc nanoparticles on SARS-CoV-2 replication and entry along with improvement of lung fibrosis induced in adult male albino rats.
Authors:El-Fakharany EM,El-Gendi H,El-Maradny YA,Abu-Serie MM,Abdel-Wahhab KG,Shabana ME,Ashry M
Journal:International journal of biological macromolecules
PubMed ID:37356684
Severe acute respiratory syndrome 2019-new coronavirus (SARS-CoV-2) is a major global challenge caused by a pandemic disease, named ‘COVID-19’ with no effective and selective therapy available so far. COVID-19-associated mortality is directly related to the inability to suppress the viral infection and the uncontrolled inflammatory response. So, we investigated the ... More
Respiratory Syncytial Virus Matrix Protein-Chromatin Association Is Key to Transcriptional Inhibition in Infected Cells.
Authors:Li HM,Ghildyal R,Hu M,Tran KC,Starrs LM,Mills J,Teng MN,Jans DA
Journal:Cells
PubMed ID:34685766
The morbidity and mortality caused by the globally prevalent human respiratory pathogen respiratory syncytial virus (RSV) approaches that world-wide of influenza. We previously demonstrated that the RSV matrix (M) protein shuttles, in signal-dependent fashion, between host cell nucleus and cytoplasm, and that this trafficking is central to RSV replication and ... More
Novel strains of a pandemic plant virus, tomato spotted wilt orthotospovirus, increase vector fitness and modulate virus transmission in a resistant host.
Authors:Chinnaiah S,Gautam S,Herron B,Workneh F,Rush CM,Gadhave KR
Journal:Frontiers in microbiology
PubMed ID:37840712
Tomato spotted wilt orthotospovirus (TSWV) is one of the most successful pandemic agricultural pathogens transmitted by several species of thrips in a persistent propagative manner. Current management strategies for TSWV heavily rely on growing single-gene resistant cultivars of tomato (“Sw-5b” gene) and pepper (“Tsw” gene) deployed worldwide. However, the emergence ... More