TaqMan™ Fast Virus 1-Step Multiplex Master Mix for qPCR (No ROX)
TaqMan™ Fast Virus 1-Step Multiplex Master Mix for qPCR (No ROX)
Applied Biosystems™

TaqMan™ Fast Virus 1-Step Multiplex Master Mix for qPCR (No ROX)

TaqMan Fast Virus 1-Step Multiplex Master Mix (No ROX) is designed to enable dye flexibility for multiplexing up to four different RNA/DNA targets for high-throughput RT-qPCR.
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Número de catálogoVolumen
55555321 x 1 mL
55555345 x 1 mL
55555361 x 10 mL
Número de catálogo 5555532
Precio (CLP)
389.454
Each
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Volumen:
1 x 1 mL
Precio (CLP)
389.454
Each
Añadir al carro de la compra

TaqMan Fast Virus 1-Step Multiplex Master Mix (No ROX) is designed to enable dye flexibility for multiplexing up to four different RNA/DNA targets for high-throughput RT-qPCR. The 4X formulation enhances detection of both RNA and DNA viral pathogens, even in the presence of challenging PCR inhibitors. TaqMan Fast Virus master mix is used for sensitive pathogen detection in research samples as well as multiplex gene expression studies with low target input. It has a single-tube format for consistent handling and processing and is ideal for high-throughput workflows, delivering results in <30 minutes.

Benefits of TaqMan Fast Virus 1-Step Multiplex Master Mix (No ROX) include:

  • Multiplexing—optimized to detect up to four RNA/DNA viral pathogen and gene expression targets
  • High sensitivity—4X master mix to amplify RNA and DNA targets at low target input levels with six logs of dynamic range
  • Tolerant to PCR inhibitors—formulated to work in the presence of common RT-qPCR inhibitors found in blood, stool, and other complex samples
  • Dye flexibility—the formulation without ROX dye enables use of other dyes in the channel previously used to measure ROX
  • Simplified application—one-tube, one-step master mix offers a single run profile with RNA and DNA and allows easy mix-and-match of targets on a plate
  • High efficiency—increased RT-qPCR speed on fast and standard instruments

Optimized for multiplexing

TaqMan Fast Virus 1-Step Multiplex Master Mix (No ROX) has been validated for detection of up to four targets simultaneously. Viral pathogen research often includes complex reactions with multiplexed primers and probes and internal controls. To meet this need, we developed this master mix for higher order multiplex reactions with multiple gene expression targets (see figure below). To simplify your experiments, a single TaqMan Fast Virus master mix protocol has been developed to amplify both types of nucleic acid, so you can interrogate both RNA and DNA virus targets next to each other on the same plate using the same handling steps.

High sensitivity

Many viral pathogen research samples have very low levels of nucleic acid targets. TaqMan Fast Virus 1-Step Multiplex Master Mix (No ROX) is optimized for highly sensitive detection of viral targets and low-titer pathogens (see figure). Formulated at a higher concentration, this master mix allows you to set up smaller reactions and run fast-cycling instruments and protocols while obtaining at least the same sensitivity as 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.

Consistent results in the presence of inhibitors

Research samples assayed for viral pathogens commonly include materials such as blood, dirt, and tissues that can inhibit qPCR reactions. TaqMan Fast Virus 1-Step Multiplex Master Mix (No ROX) includes buffer components and proprietary additives that are optimized to handle RT-qPCR inhibitors to help ensure consistent performance and provide confidence in your results. The master mix has been tested to enable robust performance in the presence of common inhibitors, including heparin, hematin, and humic acid (see figure).

Dye flexibility

TaqMan Fast Virus 1-Step Multiplex Master Mix (No ROX) does not contain the ROX passive reference dye. This allows higher order multiplexing because other dyes, such as JUN (or similar emission wavelength dye) can be measured in the channel previously used to measure ROX. Because of this flexibility, TaqMan Fast Virus master mix can be used with common real-time PCR system and allows selection of the desired passive reference dye to best fit your needs.

Fast results

TaqMan Fast Virus 1-Step Multiplex Master Mix (No ROX) speeds your time to results and streamlines the use of your real-time PCR instruments with a fast protocol. The high-concentration formulation allows for more sample containing the target nucleic acid 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.

TaqMan Fast Virus 1-Step Multiplex Master Mix (No ROX) provides robust performance, multiplexing capabilities in the presence of common RT-qPCR inhibitors, and convenient reaction setup allow you to have more confidence in your results.

Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.

Especificaciones
Para utilizar con (equipo)Sistema 7500 Fast, sistema 7500, sistema 7900HT, QuantStudio™ 12k Flex, QuantStudio™ 3, QuantStudio™ 5, QuantStudio™ 6 Flex, QuantStudio™ 6 Pro, QuantStudio™ 7 Flex, QuantStudio™ 7 Pro, StepOne™, StepOnePlus™, Viia™ 7 System
Inicio en calienteInicio en caliente integrado
Inhibitor Tolerance (Simple)High
Capacidad multiplexUp to 4-plex
N.º de reacciones200 reacción de 20 μL
Colorante de referencia pasivaNinguno
Cantidad1 x 1 mL
Tipo de muestraARN, ADN
Condiciones de envíoHielo seco
Especificidad de dianaRNA only, Both RNA and DNA
TermoestabilidadNot Applicable
Volumen1 x 1 mL
Concentración4X
Método de detecciónSonda de cebado
Para utilizar con (aplicación)Expresión génica, Detección de virus, DNA Quantitation, Presence/Absence
Método de PCRRT-qPCR de 1 paso
Velocidad de reacciónrápida o estándar
Unit SizeEach
Contenido y almacenamiento
Contiene un tubo de 1 ml de mezcla maestra 4X de RT-PCR suficiente para 200 reacciones de 20 μL.

La mezcla maestra contiene:
• ADN polimerasa de arranque en caliente AmpliTaq Fast
• Transcriptasa inversa MMLV termoestable
• dNTP
• Inhibidor de la ARNasa
• Tampón optimizado

Almacenar tubo en congelador (de –15 a –25 °C).

Preguntas frecuentes

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 (6)

Citations & References
Abstract
Enhanced detection of viruses for improved water safety.
Authors:Hayes EK,Gouthro MT,Fuller M,Redden DJ,Gagnon GA
Journal:Scientific reports
PubMed ID:37833399
Human viruses pose a significant health risk in freshwater environments, but current monitoring methods are inadequate for detecting viral presence efficiently. We evaluated a novel passive in-situ concentration method using granular activated carbon (GAC). This study detected and quantified eight enteric and non-enteric, pathogenic viruses in a freshwater recreational lake ... More
Simultaneous detection of SARS-CoV-2, influenza A, respiratory syncytial virus, and measles in wastewater by multiplex RT-qPCR.
Authors:Hayes EK,Gouthro MT,LeBlanc JJ,Gagnon GA
Journal:The Science of the total environment
PubMed ID:37201817
Utility of nasal swabs for assessing mucosal immune responses towards SARS-CoV-2.
Authors:Roubidoux EK,Brigleb PH,Vegesana K,Souquette A,Whitt K,Freiden P,St. Jude Investigative Team,Green A,Thomas PG,McGargill MA,Wolf J,Schultz-Cherry S
Journal:Scientific reports
PubMed ID:37857783
SARS-CoV-2 has caused millions of infections worldwide since its emergence in 2019. Understanding how infection and vaccination induce mucosal immune responses and how they fluctuate over time is important, especially since they are key in preventing infection and reducing disease severity. We established a novel methodology for assessing SARS-CoV-2 cytokine ... More
Passive Surveillance of SARS-CoV-2 in Adult Blacklegged Ticks (Ixodes scapularis) from Northeast Pennsylvania.
Authors:Hunt EA,Schwartz S,Chinnici N
Journal:Life (Basel, Switzerland)
PubMed ID:37763261
Monitoring the spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in wildlife is vital to public health. White-tailed deer (Odocoileus virginianus) in the United States have tested positive for SARS-CoV-2, and their interactions with blacklegged ticks (Ixodes scapularis) raise the question of whether or not these ticks also carry SARS-CoV-2. ... More
Peptide ligands targeting the vesicular stomatitis virus G (VSV-G) protein for the affinity purification of lentivirus particles.
Authors:Barbieri E,Mollica GN,Moore BD,Sripada SA,Shastry S,Kilgore RE,Loudermilk CM,Whitacre ZH,Kilgour KM,Wuestenhagen E,Aldinger A,Graalfs H,Rammo O,Schulte MM,Johnson TF,Daniele MA,Menegatti S
Journal:Biotechnology and bioengineering
PubMed ID:37947118