Make a better choice! No choosing of different qPCR master mixes anymore! One product for use with different thermal cycler simplifies the decision making process. The GNX Versa qPCR Master Mix 2X is an optimized 2-time reaction mix for real-time qPCR detection and quantitation of target DNA sequences using the SYBR®/FAM channel of most real-time qPCR instruments. It contains our HotStart Taq DNA Polymerase together with a unique passive reference dye that is compatible across a variety of instrument platforms (including those that require a high or low ROX reference signal). This dye does not spectrally overlap with fluorescent dyes used for qPCR and will not interfere with real-time detection. The master mix formulation contains all PCR components required for amplification and quantitation of DNA except primers and DNA template. Genomic DNA or cDNA can be analysed using existing as well as commercial primers.AdvantagesOne formulation for different plattformsConvenient master mix formatUser-friendly protocols simplifing reaction setupProduct performs consistently across a wide variety of sample sourceData analysisSYBR® Green binds non-specifically to double-stranded DNA. For this, the best way to check if a qPCR reaction using SYBR® Green amplified a single target without primer dimer formation is with melt-curve analysis. Melt-curve analysis is performed after a qPCR run and serves to verify that PCR amplification was specific for a single amplicon. The nonspecific binding of SYBR® Green makes melt-curve analysis one of the very few ways to confirm target-specific amplification. If the fluorescence signal generated is due to primer dimers or non-specific amplification, your relative quantification of target is at least suspect. So when starting up a new SYBR® Green PCR, always perform melt-curve analysis as a QC step to help confirm target specificity!

Lyophilized 5X Multiplex PCR Mastermix for robust PCR with all components for rapid, sensitive and reproducible quantification of DNA. The optimized DNA polymerase and an optimized buffer including our ultrapure dNTPs are key components of the ready to use mix. A hot-start formulation of the included DNA polymerase prevents false amplification during the reaction setup. Our 5X qPCR master mix will function with a wide range of templates including human-, mammal-, and plant-derived samples. Features:- 5-time concentrate for more variability in primer- and probe volumes- amplification of different targets in a single PCR tube (tested for up to 4 targets).- the hot-start formulation of the included DNA polymerase prevents false amplification during the reaction setup- the optimized buffer includes our ultrapure dNTPs Our new lyophilized Multiplex master mix for fast and easy multiplexing minimizes the need for optimization and makes the development of multiplex PCR assays fast and easy. Our new 5-fold multiplex mastermix minimizes the need for optimization and therefore makes the development and establishment of multiplex PCR easier and faster.  Read now in our blog why the 5x qPCR Multiplex MasterMix is the optimal choice for your multiplex qPCR. Our Standard Agarose LE > and especially our high resolution Agarose Tiny > are ideally suited for the subsequent electrophoresis analysis. Other realtime master mixes for your realtime PCR experiments can be found here >. Examples of Multiplex applications:F. Javier Pérez-Pérez and Nancy D. Hanson, Detection of Plasmid-Mediated AmpC β-Lactamase Genes in Clinical Isolates by Using Multiplex PCR, J. Clin. Microbiol. June 2002 vol. 40 no. 6 2153-2162. doi: 10.1128/JCM.40.6.2153-2162.2002. Tamara B. Souzaa, Diego M. Lozerb, Sônia M. S. Kitagawab, Liliana C. Spanob, Neusa P. Silvac and Isabel C. A. Scaletskya, Real-Time Multiplex PCR Assay and Melting Curve Analysis for Identifying Diarrheagenic Escherichia coli. J. Clin. Microbiol. March 2013 vol. 51 no. 3 1031-1033, doi: 10.1128/JCM.02478-12.

Introduction: Quantitative PCR is an important tool for SNP and gene expression analysis. Two general fluorescent chemistries exist for quantitative detection of gene transcripts: probes (e.g. TaqMan®, Scorpions™ Probes, molecular beacons) and DNA-binding fluorescent dyes (e.g. ethidium bromide, SYBR® Green, EvaGreen®, PicoGreen®). Ampliqon offers the RealQ Plus 2x Master Mix in two formulations: for probe or with DNA-binding fluorescent dye, making them ideal for most quantitative PCR applications. The RealQ Plus 2x Master Mixes are available with high, low or without ROX™ for optimal performance on most of the commonly used real-time PCR instruments. The RealQ Plus 2x Master Mixes promote high specificity and low background by using TEMPase Hot Start DNA Polymerase, a modified Taq DNA polymerase with hot start capabilities. The RealQ Plus 2x Master Mix Green, without ROX™, is a singletube 2x reagent including all components necessary to perform DNA-binding dye based real-time DNA amplification. Just add your primers and DNA. Detection limit: approximately 1 copy. Quantitation limit: approximately 24 copies (0.08ng of human gDNA, correlating to 12 diploid genomes, with 2 gene copies per diploid genome) Compatibility: Real-time PCR instruments with no requirement for normalization to an internal reference dye.

Introduction: Quantitative PCR is an important tool for SNP and gene expression analysis. Two general fluorescent chemistries exist for quantitative detection of gene transcripts: probes (e.g. TaqMan®, Scorpions™ Probes, molecular beacons) and DNA-binding fluorescent dyes (e.g. ethidium bromide, SYBR® Green, EvaGreen®, PicoGreen®). Ampliqon offers the RealQ Plus 2x Master Mix in two formulations: for probe or with DNA-binding fluorescent dye, making them ideal for most quantitative PCR applications. The RealQ Plus 2x Master Mixes are available with high, low or without ROX™ for optimal performance on most of the commonly used real-time PCR instruments. The RealQ Plus 2x Master Mixes promote high specificity and low background by using TEMPase Hot Start DNA Polymerase, a modified Taq DNA polymerase with hot start capabilities. The RealQ Plus 2x Master Mix Green with low ROX™ is a singletube 2x reagent including all components necessary to perform real-time DNA amplification for DNA-binding dye based PCR. Just add your primers and DNA. The ROX™ internal reference dye level is optimized for real-time instruments that require low ROX™ as internal reference dye e.g. the Stratagene Mx3005P. Detection limit: approximately 1 copy. Quantitation limit: approximately 24 copies (0.08ng of human gDNA, correlating to 12 diploid genomes, with 2 gene copies per diploid genome) ompatibility: Real-time instruments which require low ROX™ as internal reference dye e.g. the Stratagene Mx3005P.

About RealQ PCR Master Mix Quantitative polymerase chain reaction (qPCR) is the preferred method for gene analysis. RealQ PCR 2 x Master Mix is well suited for gene expression, genotyping, SNP analysis, pathogen detection, drug target validation and for measuring RNA interference. Features     - High sensitivity    - High reproducibility    - Wide dynamic range    - Premixed 2 x solution Description RealQ PCR 2 x Master Mix has undergone extensive validation to ensure high performance. Our RealQ kits contain TEMPase Hot Start DNA Polymerase, green dye and ROX reference dye. RealQ PCR Master Mix 2 x for probe is also available.

Introduction: Quantitative PCR is an important tool for SNP and gene expression analysis. Two general fluorescent chemistries exist for quantitative detection of gene transcripts: probes (e.g. TaqMan®, Scorpions™ Probes, molecular beacons) and DNA-binding fluorescent dyes (e.g. ethidium bromide, SYBR® Green, EvaGreen®, PicoGreen®). Ampliqon offers the RealQ Plus 2x Master Mix in two formulations: for probe or with DNA-binding fluorescent dye, making them ideal for most quantitative PCR applications. The RealQ Plus 2x Master Mixes are available with high, low or without ROX™ for optimal performance on most of the commonly used real-time PCR instruments. The RealQ Plus 2x Master Mixes promote high specificity and low background by using TEMPase Hot Start DNA Polymerase, a modified Taq DNA polymerase with hot start capabilities. The RealQ Plus 2x Master Mix Green with high ROX™ is a singletube 2x reagent including all components necessary to perform DNA-binding dye based real-time DNA amplification. Just add primers and DNA. ROX™ internal reference dye level is optimized for the popular StepOne and StepOnePlus instruments from Life Technologies. Detection limit: approximately 1 copy. Quantitation limit: approximately 24 copies (0.08ng of human gDNA, correlating to 12 diploid genomes, with 2 gene copies per diploid genome) Compatibility: Real-time instruments that require high ROX™ as internal reference dye e.g. StepOne and StepOnePlus from Life Technologies.

About RealQ PCR Master Mix Quantitative polymerase chain reaction (qPCR) is the preferred method for gene analysis. RealQ PCR 2 x Master Mix is well suited for gene expression, genotyping, SNP analysis, pathogen detection, drug target validation and for measuring RNA interference. Features     - High sensitivity    - High reproducibility    - Wide dynamic range    - Premixed 2 x solution Description RealQ PCR 2 x Master Mix has undergone extensive validation to ensure high performance. Our RealQ kits contain TEMPase Hot Start DNA Polymerase, green dye and ROX reference dye. RealQ PCR Master Mix 2 x for probe is also available.

About RealQ PCR Master Mix Quantitative polymerase chain reaction (qPCR) is the preferred method for gene analysis. RealQ PCR 2 x Master Mix is well suited for gene expression, genotyping, SNP analysis, pathogen detection, drug target validation and for measuring RNA interference. Features     - High sensitivity    - High reproducibility    - Wide dynamic range    - Premixed 2 x solution This Master Mix shows an Optimum performance on standard realtime instruments:      -  ABI 7500  -  Roche LightCycler™  -  Mx3000™Description RealQ PCR 2 x Master Mix has undergone extensive validation to ensure high performance. Our RealQ kits contain TEMPase Hot Start DNA Polymerase, green dye and ROX reference dye. RealQ PCR Master Mix 2 x for probe is also available.

LyoPlex Multiplex PCR master mix for fast and reliable quantification of up to 5 cDNA or gDNA targets in a single tube by multiplex, real-time PCR. This specially optimized and lyophilized master mix promotes fast multiplex real-time PCR. The combination of the specially designed hot start DNA polymerase together with a unique PCR buffer system as a lyophilized ready-to-use master mix ensures highly sensitive qPCR together with a very convenient storage at room temperature. Our new lyophilized Multiplex master mix for fast and easy multiplexing minimizes the need for optimization and makes the development of multiplex PCR assays fast and easy.- Amplification of multiple targets in a single tube (tested for up to 5 targets)- All-in-one master mix for convenient multiplexing- High specificity, sensitivity and product yield- Easy reaction setup at room temperature- stable for 24 months at room temperature The Multiplex PCR master mix is a premixed, ready-to-use solution containing our highly specific chemically modified Taq DNA Polymerase, highly pure dNTPs, MgCl2, additives and a reaction buffer at optimal concentrations which enable reliable multiplex PCR, e.g. microsatellite, clonality or gene rearrangement analysis. Just add your primers and template DNA. The Multiplex HS Master mix 2X is shipped in aliquots of 1.25mL. Our Standard Agarose LE > and especially our high resolution Agarose Tiny > are ideally suited for the subsequent electrophoresis analysis. Other realtime master mixes for your realtime PCR experiments can be found here >. Examples of Multiplex applications: F. Javier Pérez-Pérez and Nancy D. Hanson, Detection of Plasmid-Mediated AmpC β-Lactamase Genes in Clinical Isolates by Using Multiplex PCR, J. Clin. Microbiol. June 2002 vol. 40 no. 6 2153-2162. doi: 10.1128/JCM.40.6.2153-2162.2002. Tamara B. Souzaa, Diego M. Lozerb, Sônia M. S. Kitagawab, Liliana C. Spanob, Neusa P. Silvac and Isabel C. A. Scaletskya, Real-Time Multiplex PCR Assay and Melting Curve Analysis for Identifying Diarrheagenic Escherichia coli. J. Clin. Microbiol. March 2013 vol. 51 no. 3 1031-1033, doi: 10.1128/JCM.02478-12.

AQ97 Hot Start High Fidelity 2x Master Mix contains a proofreading enzyme for  robust amplification of DNA targets with low to high GC content and long DNA targets  of 18 kb. The DNA binding domain of this polymerase, ensures excellent high fidelity, long range capacity and also fast amplification results. AQ97 High Fidelity DNA Polymerase exhibits both 5'→3' DNA polymerase activity and 3'→5' proofreading exonuclease activity enabling this polymerase to correct base pair mismatches. We recommend to use our AQ97 High Fidelity 2x Master Mix with a capability of amplifying DNA targets up to 18 kb. For difficult amplicons, such as GC-rich DNA samples, those with complex secondary structures or long amplicons, the addition of 1 – 2 M Betaine Enhancer Solution is recommended. AQ97 High Fidelity DNA Polymerase is a novel proofreading DNA polymerase. AQ97 High Fidelity DNA Polymerase is a fused protein complex of DNA polymerase with a processivity-enhancing DNA binding domain. Alongside very fast and robust amplification of complex and long targets, AQ97 High Fidelity DNA Polymerase displays a high fidelity ensuring accurate amplification. The master mix is well suited for PCR experiments that require amplification with very low error rates, such as cloning/sub-cloning, NGS applications, SNP analysis and mutagenesis. Features: • High Fidelity: > 60x Taq fidelity• High elongation rate: 10 sec/kb (up to 6000bp per minute) • Built in hot start technology• Long range amplification: 18 kb for human gDNA• 5'-3' polymerase acitivity and 3'-5' exonuclease activity.• Generates blund ends.Picture 1: Comparison figures of fidelity values for AQ97 DNA Polymerase, AccuPol DNA Polymerase, and two well-recognized high fidelity DNA polymerases "P" and "Q" and Taq DNA Polymerase were determined through NGS-based analysis of nucleotide misincorporation during PCR. Initially, PCR amplification was performed on a ~ 200 bp synthetic DNA target, generating PCR products for each of the tested polymerases (using recommended setup conditions). Picture 2: Eight different human genomic DNA targets, ranging from 400 to 800 bp in length and with GC content between 29% and 78%, were amplified with AQ97 Hot Start High Fidelity DNA Polymerase 2x Master Mix. Robust amplification was observed for all targets. For targets with GC content greater than 70%, 2 M Betaine Enhancer Solution was included in the reaction mix.Picture 3: Five different targets of human genomic DNA ranging from 2 kb to 17.5 kb were amplified. Robust amplification was observed for all targets using AQ97 Hot Start High Fidelity DNA Polymerase 2x Master Mix, demonstrating the ability of the master mix to amplify large and complex targets. Amplicon sizes are indicated at the top of the gel. Marker M: High Range DNA Ladder.

The Genaxxon GNX Food Probe qPCR MasterMix 2X enables precise real-time PCR-based analysis of environmental, food and other difficult samples that may contain high levels of inhibitors. The Master Mix can be used to reliably analyse and quantify challenging applications such as the detection of low copy number templates, multiplex PCR or the sensitive detection of quantity and number limited genetic targets.FeaturesCustomised for quantitative real-time PCRUnrivalled sensitivity for demanding applicationsDetection of low copy number targets Sensitive detection for reliable quantification of limited genetic targetsStable mix for high throughput handlingOptimised formulation for unparalleled performance The Genaxxon SuperHot Taq DNA polymerase offers convenience and practicality, without compromising efficiency or specificity: 1. The chemical modification inhibits the polymerase, which prevents false priming at all temperatures tested, allowing for PCR reactions to be set up at RT (20°C to 25°C), and 2. "High mix stability allows pre-assemby of the plate in advance", which means PCR reactions can be prepared and stored at RT for up to three days before they are run, without affecting the results. The Probe qPCR master mix without ROX contains all the necessary components in an optimized composition to carry out quantitative PCR. chemically modified Taq DNA Polymerase dATP, dCTP, dGTP, dTTP optimized reaction buffer stabilizers and enhancers to enable even amplification of low copy number targets the small aliquote size of 1.25mL simplifies handling and storage (less freeze-thaw cycles per aliquote) Stability at +2°C to +8°C (refrigerator): minimum of 8 months. This Mastermix is specially suited for the following instruments: BioRad CFX96 Touch™, CFX384 Touch™, CFX Connect™, DNA Engine Opticon® 2, Chromo4™, iCycler iQ™ and My iQ™ , Roche LightCycler® 480, LightCycler® 1536, LightCycler® Nano, LightCycler® 96 and QuantStudio™ instruments, Thermo Scientific™ PikoReal™, Cepheid SmartCycler®, Bio Molecular Systems Mic qPCR cycler, Qiagen Rotor Gene Q, Rotor Gene 6000, MyGo Mini and MyGo Pro. Further realtime PCR Mastermixes and realtime FAST PCR Mastermixes can be found here: qPCR (Classic qPCR > or FAST and Multiplex qPCR >).

Lyophilized (freeze-dried) temperature stable and pre-mixed Hotstart master mix with all necessary components for probe realtime PCR (optimized buffer, dNTPs, Hotstart Taq) for difficult to amplify templates, qPCR and Multiplex applications. No cooling/cooling chain necessary! Our LyoMix and all ingredients are unopened stable at ambient temperature for at least 24 months! Our lyophilized qPCR master mix is also available as LyoBalls pre-portioned in PCR tube strips or PCR plates (M3069 > - 0.1mL tubes or M3070 > - 0.2mL tubes)! Our Hotstart Polymerase guarantees that during setup and the first PCR cycle the enzyme is not active and misprimed primers are not extended. As a result specificity and efficiency are increased by far compared to standard Taq DNA polymerase. Additionally, difficult targets with high GC-content can be amplified. The higher sensitivity improves multiplex PCR results.This lyophilized master mix in powder form is the perfect choice for a fast reaction setup that reduces the time required for pipetting and the possibility for pipetting errors. Just add PCR-grade water, template and primers to reconstitute the master mix and you are all set! Lyophilized realtime PCR master mix:• Hotstart Polymerase• increased specificity• increased sensitivity• for difficult to amplify templates with high GC content• for Multiplex applications• for qPCR• ready-to-useThis lyophilized Hotstart master mix is delivered in powder form that can be easily dispensed. With our high quality dNTPs as Set > (M3015.4100 and M3015.0250) or Mix (M3016.1010) > or our DNA Ladders > and our favourable standard agarose (M3044) > we can offer additional products for your PCR.

While using our LyoBalls there is no need for cooling anymore! The balls and all ingredients are unopened stable at ambient temperature for at least 24 months! Lyophilized (freeze-dried) temperature stable, pre-mixed and pre-dispensed Hotstart master mix with all necessary components for probe realtime PCR (optimized buffer, dNTPs, Hotstart Taq) for difficult to amplify templates, qPCR and Multiplex applications. Only PCR-grade water has to be added to get the ready-to-use PCR master mix. The lyophilized master mix is supplied in a breakable 96-well PCR plate. The plate can be divided into individual "8's strips". Thus, you have the variability to run smaller or larger preparations, depending on your needs. No cooling/cooling chain necessary! The beads and all ingredients are unopened stable at ambient temperature for at least 24 months! Our Hotstart Polymerase guarantees that during setup and the first PCR cycle the enzyme is not active and misprimed primers are not extended. As a result specificity and efficiency are increased by far compared to standard Taq DNA polymerase. Additionally, difficult targets with high GC-content can be amplified. The higher sensitivity improves multiplex PCR results.This lyophilized master mix in a easy to handle bead format is the perfect choice for a fast reaction setup that reduces the time required for pipetting and the possibility for pipetting errors. Just add  PCR-grade water, template and primers to reconstitute the master mix and you are all set!Lyophilized realtime PCR master mix:• Hotstart Polymerase• increased specificity• increased sensitivity• for difficult to amplify templates with high GC content• for Multiplex applications•    for qPCR• ready-to-useThis lyophilized Hotstart master mix is delivered in single beads that can be easily dispensed. Each bead is equivalent to one 20µL PCR reaction. Our lyophilized qPCR Probe master mix is available in powder form (LyoMix, M3071) > and pre-dispensed in a 96-well PCR plate or strips. With our high quality dNTPs as Set > (M3015.4100 and M3015.0250) or Mix (M3016.1010) > or our DNA Ladders > and our favourable standard agarose (M3044) > we can offer additional products for your PCR.

While using our LyoBalls there is no need for cooling anymore! The balls and all ingredients are unopened stable at ambient temperature for at least 24 months!  Lyophilized (freeze-dried) temperature stable, pre-mixed and pre-dispensed Hotstart master mix with all necessary components for probe realtime PCR (optimized buffer, dNTPs, Hotstart Taq) for difficult to amplify templates, qPCR and Multiplex applications. Only PCR-grade water has to be added to get the ready-to-use PCR master mix. The lyophilized master mix is supplied in a "break-a-way" 96-well PCR plate. The plate can be divided into individual "8's strips". Thus, you have the variability to run smaller or larger preparations, depending on your needs. No cooling/cooling chain necessary! The beads and all ingredients are unopened stable at ambient temperature for at least 24 months! Our Hotstart Polymerase guarantees that during setup and the first PCR cycle the enzyme is not active and misprimed primers are not extended. As a result specificity and efficiency are increased by far compared to standard Taq DNA polymerase. Additionally, difficult targets with high GC-content can be amplified. The higher sensitivity improves multiplex PCR results.This lyophilized master mix in a easy to handle bead format is the perfect choice for a fast reaction setup that reduces the time required for pipetting and the possibility for pipetting errors. Just add  PCR-grade water, template and primers to reconstitute the master mix and you are all set!Lyophilized realtime PCR master mix:•    Hotstart Polymerase•    increased specificity•    increased sensitivity•    for difficult to amplify templates with high GC content•    for Multiplex applications•    for qPCR•    ready-to-useThis lyophilized Hotstart master mix is delivered in single beads that can be easily dispensed. Each bead is equivalent to one 20µL PCR reaction. Our lyophilized qPCR Probe master mix is available in powder form (LyoMix, M3071) > and pre-dispensed in a breakable 96-well PCR plate. With our high quality dNTPs as Set > (M3015.4100 and M3015.0250) or Mix (M3016.1010) > or our DNA Ladders > and our favourable standard agarose (M3044) > we can offer additional products for your PCR.

ProbeMasterMix FAST with 500nM  ROX optimised for fast realtime PCR assays in block systems. This master mix is ready-to-use and contains all components for a successful and reliable quantitative PCR with the exception of primer and template DNA. Advantages of the Hotstart Taq polymerase used in the Genaxxon ProbeMasterMix: Hotstart technology enables setup of PCR mixture at room temperature. short initial denaturation of not more than 2 minutes. optimized for 2-step PCR protocols. No pipetting on ice necessary anymore No immediate further processing (PCR) necessary. The pipetted pre-PCR mixtures can be left at RT for up to 3 days. Amplification of GC-rich templates High yields No Primer dimers The Genaxxon Hotstart Taq DNA polymerase offers convenience and practicality, without compromising efficiency or specificity: 1. The hotstart formulation inhibits the polymerase, which prevents false priming at all temperatures tested, allowing for PCR reactions to be set up at RT (20°C to 25°C), and 2. High mix stability allows pre-assemby of the plate in advance", which means PCR reactions can be prepared and stored at RT for up to three days before they are run, without affecting the results. The Probe qPCR master mix with 500nM ROX contains all the necessary components in an optimized composition to carry out quantitative PCR. hotstart Taq DNA Polymerase dATP, dCTP, dGTP, dTTP optimized reaction buffer 500nM ROX as internal reference stabilizers and enhancers to enable even amplification of low copy number targets the small aliquote size of 1.25mL simplifies handling and storage (less freeze-thaw cycles per aliquote) This Mastermix is specially suited for the following instruments: Applied Biosystems® 5700, 7000, 7300, 7700, 7900, 7900 HT, Eppendorf Realplex4, StepOne™ and StepOnePlus™. Further realtime PCR Mastermixes and realtime FAST PCR Mastermixes can be found here: qPCR (Classic qPCR > or FAST and Multiplex qPCR >).

GreenMasterMix FAST without ROX is optimised for fast qPCR assays without probes in block systems. The master mix is optimized for fast PCR with short denaturation 2-step cycles. This 2X Mastermix is ready-to-use and contains all components for a successful and reliable qPCR with the exception of primer and template DNA. Advantages of the HotStart Taq DNA polymerase used in the Genaxxon GreenMasterMix: Hotstart technology enables setup of PCR mixture at room temperature. short initial denaturing time of not more than 2 minutes No pipetting on ice necessary anymore No immediate further processing (PCR) necessary. The pipetted pre-PCR mixtures can be left at RT for up to 3 days. Amplification of GC-rich templates High yields No Primer dimers The Genaxxon SuperHot Taq DNA polymerase offers convenience and practicality, without compromising efficiency or specificity: 1. The chemical modification inhibits the polymerase, which prevents false priming at all temperatures tested, allowing for PCR reactions to be set up at RT (20°C to 25°C), and 2. "High mix stability allows pre-assemby of the plate in advance", which means PCR reactions can be prepared and stored at RT for up to three days before they are run, without affecting the results. The Green qPCR master mix without ROX contains all the necessary components in an optimized composition to carry out quantitative PCR: chemically modified Taq DNA Polymerase dATP, dCTP, dGTP, dTTP intercalating green fluorescent dye optimized reaction buffer stabilizers and enhancers to enable even amplification of low copy number targets the small aliquote size of 1.25mL simplifies handling and storage (less freeze-thaw cycles per aliquote) Stability at +2°C to +8°C (refrigerator): minimum of 8 months. This Mastermix is specially suited for the following instruments: BioRad CFX96 Touch™, CFX384 Touch™, CFX Connect™, DNA Engine Opticon® 2, Chromo4™, iCycler iQ™ and My iQ™ , Roche LightCycler® 480, LightCycler® 1536, LightCycler® Nano, LightCycler® 96 and QuantStudio™ instruments, Thermo Scientific™ PikoReal™, Cepheid SmartCycler®, Bio Molecular Systems Mic qPCR cycler, Qiagen Rotor Gene Q, Rotor Gene 6000, MyGo Mini and MyGo Pro. Further realtime PCR Mastermixes and realtime FAST PCR Mastermixes can be found here: qPCR (Classic qPCR > or FAST and Multiplex qPCR >).

ProbeMasterMix FAST without ROX is optimised for fast qPCR assays with probes in block systems. The master mix is optimized for fast PCR with short denaturation 2-step cycles. This 2X Mastermix is ready-to-use and contains all components for a successful and reliable qPCR with the exception of primer and template DNA. Advantages of the Hotstart Taq polymerase used in the Genaxxon ProbeMasterMix: Hotstart technology enables setup of PCR mixture at room temperature. short initial denaturation of not more than 2 minutes. optimized for 2-step PCR protocols. No pipetting on ice necessary anymore No immediate further processing (PCR) necessary. The pipetted pre-PCR mixtures can be left at RT for up to 3 days. Amplification of GC-rich templates High yields No Primer dimers The Genaxxon Hotstart Taq DNA polymerase offers convenience and practicality, without compromising efficiency or specificity: 1. The hotstart formulation inhibits the polymerase, which prevents false priming at all temperatures tested, allowing for PCR reactions to be set up at RT (20°C to 25°C), and 2. High mix stability allows pre-assemby of the plate in advance", which means PCR reactions can be prepared and stored at RT for up to three days before they are run, without affecting the results. The Probe qPCR master mix without ROX contains all the necessary components in an optimized composition to carry out quantitative PCR. hotstart Taq DNA Polymerase dATP, dCTP, dGTP, dTTP optimized reaction buffer stabilizers and enhancers to enable even amplification of low copy number targets the small aliquote size of 1mL simplifies handling and storage (less freeze-thaw cycles per aliquote) This Mastermix is specially suited for the following instruments: BioRad CFX96 Touch™, CFX384 Touch™, CFX Connect™, DNA Engine Opticon® 2, Chromo4™, iCycler iQ™ and My iQ™ , Roche LightCycler® 480, LightCycler® 1536, LightCycler® Nano, LightCycler® 96 and QuantStudio™ instruments, Thermo Scientific™ PikoReal™, Cepheid SmartCycler®, Bio Molecular Systems Mic qPCR cycler, Qiagen Rotor Gene Q, Rotor Gene 6000, MyGo Mini and MyGo Pro. Further realtime PCR Mastermixes and realtime FAST PCR Mastermixes can be found here: qPCR (Classic qPCR > or FAST and Multiplex qPCR >).

GreenMasterMix FAST with 500nM ROX is optimised for realtime PCR assays in block systems. This 2X Mastermix is ready-to-use and contains all components for a successful and reliable qPCR with the exception of primer and template DNA. Advantages of the HotStart Taq DNA polymerase used in the Genaxxon GreenMasterMix: Hotstart technology enables setup of PCR mixture at room temperature. short initial denaturing time of not more than 2 minutes No pipetting on ice necessary anymore No immediate further processing (PCR) necessary. The pipetted pre-PCR mixtures can be left at RT for up to 3 days. Amplification of GC-rich templates High yields No Primer dimers The Genaxxon SuperHot Taq DNA polymerase offers convenience and practicality, without compromising efficiency or specificity: 1. The chemical modification inhibits the polymerase, which prevents false priming at all temperatures tested, allowing for PCR reactions to be set up at RT (20°C to 25°C), and 2. "High mix stability allows pre-assemby of the plate in advance", which means PCR reactions can be prepared and stored at RT for up to three days before they are run, without affecting the results. The Green qPCR master mix with 500nM ROX contains all the necessary components in an optimized composition to carry out quantitative PCR: chemically modified Taq DNA Polymerase dATP, dCTP, dGTP, dTTP intercalating green fluorescent dye optimized reaction buffer stabilizers and enhancers to enable even amplification of low copy number targets the small aliquote size of 1.25mL simplifies handling and storage (less freeze-thaw cycles per aliquote) This Mastermix is specially suited for the following instruments: Applied Biosystems® 5700, 7000, 7300, 7700, 7900, 7900 HT, Eppendorf Realplex4, StepOne™ and StepOnePlus™. Further realtime PCR Mastermixes and realtime FAST PCR Mastermixes can be found here: qPCR (Classic qPCR > or FAST and Multiplex qPCR >).

GreenMasterMix FAST with 50nM ROX is optimised for realtime PCR assays in block systems. This 2X Mastermix is ready-to-use and contains all components for a successful and reliable qPCR with the exception of primer and template DNA. Advantages of the HotStart Taq DNA polymerase used in the Genaxxon GreenMasterMix: Hotstart technology enables setup of PCR mixture at room temperature. short initial denaturing time of not more than 2 minutes No pipetting on ice necessary anymore No immediate further processing (PCR) necessary. The pipetted pre-PCR mixtures can be left at RT for up to 3 days. Amplification of GC-rich templates High yields No Primer dimers The Genaxxon SuperHot Taq DNA polymerase offers convenience and practicality, without compromising efficiency or specificity: 1. The chemical modification inhibits the polymerase, which prevents false priming at all temperatures tested, allowing for PCR reactions to be set up at RT (20°C to 25°C), and 2. "High mix stability allows pre-assemby of the plate in advance", which means PCR reactions can be prepared and stored at RT for up to three days before they are run, without affecting the results. The Green qPCR master mix with 50nM ROX contains all the necessary components in an optimized composition to carry out quantitative PCR: chemically modified Taq DNA Polymerase dATP, dCTP, dGTP, dTTP intercalating green fluorescent dye optimized reaction buffer stabilizers and enhancers to enable even amplification of low copy number targets 50nM internal passive reference fluorescence dye the small aliquote size of 1.25mL simplifies handling and storage (less freeze-thaw cycles per aliquote) This Mastermix is specially suited for the following instruments: Applied Biosystems® 7500, 7500 Fast and ViiA™ 7, QuantStudio™ instruments, Agilent Mx3000P™, Mx3005P™, Mx4000™ and AriaMx. Other realtime PCR master mixes from Genaxxon are: M3023 - GreenMastermix No ROX >, M3045 - ProbeMastermix No ROX >, M3011 - GreenMastermix Low ROX >, M3031 - ProbeMastermix Low ROX >, M3052 - GreenMastermix High ROX >, M3010 - ProbeMastermix High ROX >.