PCR Master Mixes - PCR Kits - PCR Master mixes

For reliable and easy PCR: PCR Master Mix for standard PCR applications (e.g. screenings) for amplifying DNA fragments <5kb. It is a premixed, ready-to-use solution containing Taq DNA Polymerase, dNTPs, MgCl2 and reaction buffers at optimal concentrations for efficient amplification of DNA templates by routine PCR (one tube, one pipetting step). Just add your primers and template DNA - that´s all.  The special formulation of our PCR Master Mix guarantees you reproducible results even after repeated freezing/thawing steps leading to good yields and sensitivity. The PCR Master Mix is efficient (no left over of reagents), scalable from 10µL to 50µL and stable for 24 months. Test sample available at a special price! The test sample price will be refunded on the first official order of the product.   Our Agaroses > and DNA Ladders > are ideally suited for subsequent electrophoresis of PCR products.

SimplyEnlight PCR Starter-Kit – The All-in-One Solution for Efficient PCRFrom PCR to gel electrophoresis to visualization – all in just one preparation step!No additional pipetting of buffers or stains required. Save time and minimize contamination risks with the SimplyEnlight PCR Starter-Kit! Our innovative Red MasterMix Fluoro (2X) streamlines the PCR workflow by combining PCR amplification, gel loading dye, and nucleic acid staining in a single reaction. Additionally, the kit includes the pre-stained GenLadder 100 bp Plus, eliminating the need for extra staining.Your Key Benefits:Fast & efficient workflow – just one preparation step requiredNo additional gel staining – integrated fluorescent DNA stain for instant visualizationReduced contamination risk – fewer pipetting steps, improved reproducibilityNon-toxic fluorescent dye – environmentally friendly and safe disposalOptimized for screening & high-throughput applications – ideal for colony PCR and routine analysisContents of the SimplyEnlight PCR Starter-Kit: Red MasterMix Fluoro (2X) – the 3-in-1 solution: PCR MasterMix with DNA polymerase, buffer, dNTPs & MgCl₂ Integrated red loading dye for pipetting control Built-in fluorescent nucleic acid stain – no additional staining required GenLadder 100 bp Plus – pre-stained DNA marker:Instant DNA band visualization under UV or blue light No separate staining or pipetting required Loading Buffer I Fluoro (6X) – for additional DNA markers: Flexible use for staining extra DNA markers It doesn’t get any easier! With the SimplyEnlight PCR Starter-Kit, just mix your DNA and primers with the Red MasterMix Fluoro (2X) and start your PCR. After amplification, the PCR product can be analyzed and visualized via gel electrophoresis without any additional staining. Optimize your PCR workflow – with the SimplyEnlight PCR Starter-Kit from Genaxxon!

Highly specific Hotstart master mix for routine and diagnostic PCR and qPCR up to 4kb: ready-to-use master mix with chemical modified Taq DNA polymerase. This Hotstart Master Mix for qPCR is a premixed, ready-to-use solution containing chemically modified Taq DNA Polymerase, dNTPs, MgCl2 and reaction buffers at optimal concentrations for efficient amplification of DNA templates by PCR and qPCR (one tube, one pipetting step). Just add your primers and template DNA. The Hotstart PCR Master Mix has been optimized for use in routine and diagnostic Hotstart PCR and qPCR for amplifying DNA template in the range of 0.2-4kb. The special formulation of our Hotstart Master Mix guarantees you reproducible results even after repeated freezing/thawing steps leading to good yields and sensitivity. The Hotstart Master Mix is efficient (no left over of reagents), scalable from 10µL to 50µL and stable for 12 months. This Hotstart PCR master mix is also available as SuperHot Mastermix Blue > enabling visualisation of each pipetting step. With our high quality dNTPs as Set (M3015.4100 and M3015.0250) > or Mix (M3016.1010) > or our DNA Ladders > and favourable standard agarose (M3044) > we can offer additional products for your PCR.

RedMasterMix (2x) - PCR MasterMix with red dye to help visualize pipetting and mixing steps. Electrophoresis can be performed immediately after PCR without the need of a gel loading buffer. This makes this MasterMix time efficient, cost efficient and a reliable choice for the best PCR results with high efficiency.  One tube, one pipetting step. RedMasterMix (2x) is delivered to you as a optimized, ready-to-use solution containing- Taq DNA Polymerase - dNTPs- MgCl2- a red dye- reaction bufferfor efficient amplification of DNA. Additionally the RedMasterMix (2x) contains an additive and a red dye for proceeding with electrophoresis after PCR without adding loading buffer. Just add your primers and template DNA. This PCR MasterMix (2x) has been optimized for use in routine PCR amplification of DNA templates in the range of 0.2-4kb. The special formulation of our PCR RedMasterMix (2x) can withstand repeated freezing/thawing without compromising yields, sensitivity or results, when used as directed. The PCR MasterMix with red dye is efficient (no left over of reagents), scalable from 10µL to 50µL and stable for at least 24 months.Our RedMastermix can also be used for Sanger sequencing. Just dilute the PCR reaction 1:8 after PCR, or purify using spin columns and then apply. Read now in our blog how Genaxxon's RedMasterMix can also simplify your laboratory work. Our Agaroses > and DNA Ladders > are ideally suited for subsequent electrophoresis of PCR products.

ready-to-use PCR Mastermix with red Loading Dye for visual control of the pipetting steps and additional fluorescent dye for fast and easy detection of the DNA bands. After PCR, the PCR mix can be pipetted directly into the gel pockets without adding loading buffer. This makes our RedMasterMix Fluoro (2x) even more time- and cost-saving than our proven Red Mastermix. The RedMasterMix Fluoro (2x) with fluorescent gel staining dye and red loading dye also features high specificity for best results. The RedMasterMix Fluoro (2x) is a ready-to-use mixture of: - Taq DNA Polymerase- PCR reaction buffer- dNTPs- MgCl2- red loading dye- fluorescence gel staining dye for DNA band detection in an optimal concentration for efficient amplification of DNA templates by PCR. Only the primers and the template DNA have to be added. At the same time, the PCR Matermix contains an additive and a red dye, which allows subsequent electrophoresis without the addition of loading buffer. After electrophoresis, detection is performed directly under blue light without further staining. This saves additional time and costs. The RedMasterMix Fluoro (2x) with fluorescent dye was developed for use in routine PCR up to 4 kb amplicon length. The special composition of the buffer guarantees reproducible results even after repeated thawing and freezing cycles. Our Red MasterMix (2x) Fluoro is shipped in convenient aliquots of 1.25mL. For more information on our SimplyEnlight PCR products, read our blog now. Genaxxon's SimplyEnlight PCR - Unlock the Power of Your PCR!

The RedMastermix Hot (2x) from Genaxxon for fast and easy PCR setup and high reproducibility in standardized applications (Colony PCR, High-throughput PCR, Automated PCR applications). The Mastermix contains a red dye that allows direct application of the PCR product to the gel. The red dye enables monitoring of the gel run. Compared to standard Taq PCR mastermixes, the hotstart polymerase and the optimized buffer mixture with MgCl2 and dNTP results in an increased yield of amplicons up to 6kb even under Fast PCR conditions. Highly specific Hotstart Mastermix for routine applications. FAST PCR amplification up to 2kb. Ready-to-use, consisting of: Antibody inhibited Taq DNA Polymerase optimized PCR-Puffer dNTPs MgCl2 for your HotStart PCR. Ready-to-use Hotstart Mastermix. All you have to do is add the primers and the template DNA. The special composition of the buffer guarantees reproducible results even after repeated thawing and freezing cycles. The Hotstart Mastermix will be sent in 1mL aliquots. With our high quality dNTPs as Set (M3015.4100 and M3015.0250) > or Mix (M3016.1010) > or our DNA Ladders > and favourable standard agarose (M3044) > we can offer additional products for your PCR.

PCR Hotstart Master mix with blue dye: for the visual control of pipetting steps after PCR, electrophoresis can be operated without the addition of loading buffer. This makes this PCR master mix saving time and money. This Hotstart Master Mix for qPCR is a premixed, ready-to-use solution containing chemically modified Taq DNA Polymerase, dNTPs, MgCl2, a blue dye and reaction buffers at optimal concentrations for efficient amplification of DNA templates by PCR and qPCR (one tube, one pipetting step). Just add your primers and template DNA. The addition of the blue loading dye enables direct application of the PCR reaction onto a Gel. The Hotstart PCR Master Mix has been optimized for use in routine and diagnostic Hotstart PCR and qPCR for amplifying DNA template in the range of 0.2-4kb. The special formulation of our Hotstart Master Mix guarantees you reproducible results even after repeated freezing/thawing steps leading to good yields and sensitivity. The Hotstart Master Mix with blue dye is efficient (no left over of reagents), scalable from 10µL to 50µL and stable for 12 months. Hotstart Mastermix with blue dye for 200 x 25µL reactions (2.5mL). This Hotstart PCR master mix is also available as SuperHot Mastermix > enabling visualisation of each pipetting step. With our high quality dNTPs as Set (M3015.4100 and M3015.0250) > or Mix (M3016.1010) > or our DNA Ladders > and favourable standard agarose (M3044) > we can offer additional products for your PCR.

AQ97 High Fidelity DNA Polymerase ist eine proofreading Polymerase mit hoher Amplifikationsgeschwindigkeit und sehr hoher Genauigkeit (>60-fach) gegenüber Taq DNA Polymerase. AQ97 ist ideal für schwierige Targets mit sehr niedrigem oder hohem GC-Gehalt geeignet. Neben diesen Eigenschaften zeichnet sich die AQ97 auch durch Ihre Eignung, lange Targets bis zu 18 kb, zu amplifizieren aus. Dies führt zu sehr genauen und zuverlässigen PCR-Ergebnissen.  AQ97 High Fidelity DNA Polymerase besitzt sowohl eine 5'→3' DNA Polymerase-Aktivität als auch eine 3'→5' proofreading Exonuklease-Aktivität, die es dieser Polymerase ermöglicht, Basenpaar-Fehlpaarungen zu korrigieren. AQ97 High Fidelity DNA Polymerase ist ein fusionierter Proteinkomplex aus DNA-Polymerase mit einer prozessivitätssteigernden DNA-Bindungsdomäne. Neben einer sehr schnellen und robusten Amplifikation komplexer und langer Zielmoleküle zeichnet sich die AQ97 High Fidelity DNA Polymerase durch eine hohe Genauigkeit aus, was dazu führt, dass auch für lange Amplicons eine genaue Amplifikation gewährleistet ist. Dadurch eignet sich die AQ97 besonders für PCR-Experimente, die eine Amplifikation mit sehr niedrigen Fehlerraten erfordern, wie z. B. Klonen/Subklonen, NGS-Anwendungen, SNP-Analysen und Mutagenese. Eigenschaften: • High Fidelity: >60x Taq fidelity• High elongation rate: 10 sec/kb (bis 6000bp pro Minute)• 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, 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: Distribution of substitution errors. PCR was performed using Taq DNA Polymerase, AQ97 High Fidelity DNA Polymerase, high fidelity DNA Polymerase Q and high fidelity DNA Polymerase P. The PCR was followed by NGS sequencing of the PCR products. The number of substitutions at each PCR target position was calculated and plotted in diagram A. Substitutions include misincorporated nucleotides and deletions at each position. Non-polymerase errors are subtracted from the total number of errors to revel true polymerase errors. Non-polymerase errors include mutations caused by thermocycling-induced DNA damage, pre-NGS sample preparation and sequencing errors. In these diagrams the average number of substitutions for Taq DNA Polymerase (Taq average) and for AQ97 High Fidelity DNA Polymerase (AQ97 average) is also plotted. Diagram B magnifies the area near the detection limit, displaying more information about the number of substitutions for AQ97 High Fidelity DNA Polymerase, high fidelity DNA Polymerase Q and high fidelity DNA polymerase P. Click to enlarge diagrams.  

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.

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).- fast start function due to a hot-start aptamer formulation.- 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.

Multiplex PCR is a method that enables amplification of two or more amplicons simultaneously in a single reaction tube/reaction. It is widely used in genotyping and different areas of DNA testing in research, forensic and diagnostic laboratories. Our Multiplex HS Mastermix (2X) is an optimized ready-to-use mixture for probe-based assays such as TaqMan®, Beacons and MGBs. It contains a modified fast HotStart Taq DNA Polymerase, dNTPs and MgCl₂ combined in an optimized buffer system for realtime PCR / qPCR applications except primers, probe and template DNA / cDNA.  The HotStart Taq Polymerase is based on the standard Taq DNA polymerase from Genaxxon inactivated by an specific antibody against Taq DNA polymerase which is activated by heat treatment. Thus, during setup and the first ramp of thermal cycling, the enzyme is not active and misprimed primers are not extended. The result is higher specificity, increased sensitivity and greater yields when compared to standard DNA polymerases, making this enzyme especially well-suited for multiplex PCR. - Amplification of multiple targets in a single tube- All-in-one master mix for convenient multiplexing- High specificity, sensitivity and product yield- Easy reaction setup at room temperature The Multiplex HS Master mix 2X is shipped in aliquots of 1mL. 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.

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.  Stability- the lyophilized MasterMix is stable for 3 years, if stored at -20°C.- the lyophilized MasterMix is stable for at least 12 months, if stored after delivery at +15°C to+30°C.- the reconstituted MasterMix is stable for 6 months, if stored at -20°C. 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.

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.

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.

The SNP Pol DNA polymerase > used for the SNP Pol 2X Mastermix has been specially designed for easy, reliable and rapid allele-specific discrimination, eg. CRISPR / Cas9 point mutations, for detecting incorrect CRISPR / Cas9 products, or validating sequencing results. The SNP Pol DNA polymerase distinguishes highly specific, whether a mismatch of the primer-template-complex is present or not. The mismatch (point mutation) must be at the 3 'end of the primer. Thus, mutant alleles can be distinguished exactly from wild-type alleles - without sequencing, since the polymerase simply does not amplify in the case of a mismatch. Just place your primer on the supposed point mutation (Important: The point mutation must be at the 3 'end) and the polymerase will detect a mismatch in this region with almost 100% accuracy: If the template base complementary to the 3' end of the primer shows the mutation and the primer does not, no amplification takes place - 100% certainty within a short time!The SNP Pol DNA polymerase can therefore be easily, time and cost-effectively used for the screening of point mutations. The variant SNP PolTaq DNA polymerase has 5'-3 'nuclease activity and can therefore be used for specific hydrolysi probes such as Taqman® probes or Molecular beacons. For more information on our SNP DNA polymerases and applications, read our blog now. DescriptionSNP Pol DNA Polymerase and SNP PolTaq Polymerase are  highly selective DNA polymerase for the detection of Single Nucleotide Polymorphisms. It was developed specifically for allele-specific discrimination, where a very high discrimination rate is required e.g., in allele-specific PCR (ASA; AS-PCR), allele-specific primer extension (AS-PEX), SNP analysis, genotyping or in methylation-specific PCRs (MSP). Many other DNA polymerases tolerate mismatched primer-template complexes and are therefor not suitable. The SNP Pol DNA polymerase, on the other hand, distinguishes these specifically (high discrimination) and supplies only PCR products with perfectly matching primer pairs! The Genaxxon SNP Pol and SNP PolTaq DNA polymerases differ up to 100% by means of allele-specific PCR between the two alleles and, after a simple qPCR, give a clear result as to which allele is present. Thus, the principly great potential of the CRISPR/Cas9 technology can be used for human medicine and plant biotechnology especially together with the SNP PolTaq or SNP Pol DNA polymerase. Allele-specific PCR can be used to quantify the mutation rate in a pool or background of wild-type sequences. The verification of mutation frequencies determined by NGS can also be verified by means of allele-specific PCR and SNP Pol DNA polymerase. The SNP PolTaq DNA polymerase is very suitable for the analysis of liquid biopsy samples. With SNP PolTaq, the presence and frequency of cancer mutations can be analyzed and quantified very well. Picture below: Application note SNP Pol DNA Polymerase   We recommend short amplicon length (about 60-200 bp) for best results, but also longer amplicon lengths are possible. The addition of additional Magnesium (+0.5 - 1.5mM) might be needed in case of longer amplicons >500 bp.Trouble shooting: No bands after PCR of 30 cycles! Optimisation procedure for missing or weak bands.Annealing temperature is too low! Attention: The SNP Pol is an aptamer inhibited DNA polymerase. The aptamer oligo used reversibly inhibits the polymerase at temperatures <55°C! Therefore, the primers should ideally have an annealing temperature of >57°C. - realtime PCR approach - Check the dNTP concentration. This should be between 200 and 300µM (in the PCR). - Increase the number of cycles (at least 35, preferably equal to 40) Test optimisation - number of cyclesIn endpoint detection, a cycle count of 30 is not always sufficient to generate a clearly visible band. For example, with less than 200 DNA copies as a starting value. The test should therefore be run using real-time PCR, or five parallel PCRs should be used, one of which is taken from the PCR device after each of five different cycles (example below). Endpoint detection: Set up five identical PCR reactions in parallel using the SNP Pol DNA polymerase. Remove one of the PCR tubes from the cycler at each of 20, 25, 30, 35 and 40 cycles and apply all five reactions to an agarose gel at the end. This makes it easy to recognise which is the optimum number of cycles in the PCR for the given application (starting material, target, primer). SNP Pol PCR with cell lysates Animal cells and E.coli can be used directly for PCR with the SNP Pol DNA polymerase! No separate lysis or proteinase K digestion is necessary. PCR procedure:1. 50 - 500 cells are required per PCR batch! 2. prepare PCR mix with primers and buffer and place on ice! 3. add the picked colony directly to 10-20µL water (no separate lysis and no proteinase K digestion), vortex briefly (5 seconds), then add this cell suspension directly to the PCR reaction mixture, e.g. 10µL cell suspension for a PCR preparation with a total volume of 20µL. An initial denaturation time of 2-3 minutes is sufficient is sufficient, can be extended to 5 minutes if necessary. Genomic DNA per reaction max. 100 copies is relatively low, but should still work. The remainder of this cell suspension can also be frozen away in order to carry out further tests. Optional: 4. if possible: do real-time PCR!The SNP Pol DNA polymerase (M3009 > or M3061 >) can be used together with non-specific fluorescent dyes (eg Genaxxon's Green DNA Dye > or SybrGreen®) in real-time PCR. When working with specific PCR probes, only the SNP PolTaq DNA polymerase can be used, since only these have a 5'-3 'exonuclease activity. With our high quality dNTPs as Set (M3015.4100) > or Mix (M3016.1010) > or our DNALadders > and our favourable standard agarose (M3044) > we can offer additional products for your PCR. Application areas for SNP Pol DNA and SNP Pol DNA polymerase- Monitoring, verification and detection of point mutations- Identification of correct or wrong CRISPR/Cas9 products- Verification/validation of sequencing results- Quantification of mutations (e.g. NGS results)- SNP-detection by allele-specific amplification (ASA) / Allele-specific PCR- Methylation specific PCRs (MSP) after bisulfite treated DNA (CpG methylation sides)- HLA genotyping- micro sequencing- realtime PCR with hydrolysis probes- realtime multiplex PCRs - DamID-seq data in C. elegans. As an alternative to ChIP, DNA adenine methyltransferase identification by sequencing (DamID-seq) was recently shown to be able to characterize binding sites in single mammalian cells. Additionally, DamID can be achieved for cell-type specific analysis by expressing Dam fusion proteins under tissue specific promoters in a controlled manner. In this report, we present a user-friendly pipeline to analyse DamID-seq data in C. elegans. Sharma R, Ritler D, Meister P.Tools for DNA adenine methyltransferase identification analysis of nuclear organization during C. elegans development. Genesis. 2016 Feb 4. doi: 10.1002/dvg.22925. - Minisequencing SNP genotyping with SNPase DNA Polymerase can be carried out by the procedure described in: Lovmar L, Fredriksson M, Liljedahl U, Sigurdsson S, Syvänen AC. Quantitative evaluation by minisequencing and microarrays reveals accurate multiplexed SNP genotyping of whole genome amplified DNA. Nucleic Acids Res. 2003;31:e129. - Allel specific mismatch selectivity by the HiDi DNA polymerase Drum M, Kranaster R, Ewald C, Blasczyk R, Marx A (2014) Variants of a Thermus aquaticus DNA Polymerase with Increased Selectivity for Applications in Allele- and Methylation-Specific Amplification. PLoS ONE 9(5): e96640. doi:10.1371/journal.pone.0096640

The SNP PolTaq DNA polymerase used for the SNP PolTaq 2X Master Mix has been specially designed for easy, reliable and rapid allele-specific discrimination, eg. CRISPR / Cas9 point mutations, for detecting incorrect CRISPR / Cas9 products, or validating sequencing results. The SNP PolTaq DNA polymerase distinguishes highly specific, whether a mismatch of the primer-template-complex is present or not. The mismatch (point mutation) must be at the 3 'end of the primer. Thus, mutant alleles can be distinguished exactly from wild-type alleles - without sequencing, since the polymerase simply does not amplify in the case of a mismatch. Just place your primer on the supposed point mutation (Important: The point mutation must be at the 3 'end) and the polymerase will detect a mismatch in this region with almost 100% accuracy: If the template base complementary to the 3' end of the primer shows the mutation and the primer does not, no amplification takes place - 100% certainty within a short time!The SNP PolTaq DNA polymerase can therefore be easily, time and cost-effectively used for the screening of point mutations. The SNP PolTaq DNA polymerase has 5'-3 'nuclease activity and can therefore be used for specific hydrolysi probes such as Taqman® probes or Molecular beacons. For more information on our SNP DNA polymerases and applications, read our blog now. DescriptionSNP PolTaq DNA polymerase is a highly selective DNA polymerase for the detection of Single Nucleotide Polymorphisms. It was developed specifically for allele-specific discrimination, where a very high discrimination rate is required e.g., in allele-specific PCR (ASA; AS-PCR), allele-specific primer extension (AS-PEX), SNP analysis, genotyping or in methylation-specific PCRs (MSP). Many other DNA polymerases tolerate mismatched primer-template complexes and are therefor not suitable. The SNP PolTaq DNA polymerase, on the other hand, distinguishes these specifically (high discrimination) and supplies only PCR products with perfectly matching primer pairs! The Genaxxon SNP Pol and SNP PolTaq DNA polymerases differ up to 100% by means of allele-specific PCR between the two alleles and, after a simple qPCR, give a clear result as to which allele is present. Thus, the principly great potential of the CRISPR/Cas9 technology can be used for human medicine and plant biotechnology especially together with the SNP PolTaq or SNP Pol DNA polymerase. Allele-specific PCR can be used to quantify the mutation rate in a pool or background of wild-type sequences. The verification of mutation frequencies determined by NGS can also be verified by means of allele-specific PCR and SNP Pol DNA polymerase. The SNP PolTaq DNA polymerase is very suitable for the analysis of liquid biopsy samples. With SNP PolTaq, the presence and frequency of cancer mutations can be analyzed and quantified very well. Picture below: Application note SNP Pol DNA Polymerase   We recommend short amplicon length (about 60-200 bp) for best results, but also longer amplicon lengths are possible. The addition of additional Magnesium (+0.5 - 1.5mM) might be needed in case of longer amplicons >500 bp.Trouble shooting: No bands after PCR of 30 cycles! Optimisation procedure for missing or weak bands.Annealing temperature is too low! Attention: The SNP PolTaq is an aptamer inhibited DNA polymerase. The aptamer oligo used reversibly inhibits the polymerase at temperatures <55°C! Therefore, the primers should ideally have an annealing temperature of >57°C. - realtime PCR approach - Check the dNTP concentration. This should be between 200 and 300µM (in the PCR). - Increase the number of cycles (at least 35, preferably equal to 40) Test optimisation - number of cyclesIn endpoint detection, a cycle count of 30 is not always sufficient to generate a clearly visible band. For example, with less than 200 DNA copies as a starting value. The test should therefore be run using real-time PCR, or five parallel PCRs should be used, one of which is taken from the PCR device after each of five different cycles (example below). Endpoint detection: Set up five identical PCR reactions in parallel using the SNP Pol DNA polymerase. Remove one of the PCR tubes from the cycler at each of 20, 25, 30, 35 and 40 cycles and apply all five reactions to an agarose gel at the end. This makes it easy to recognise which is the optimum number of cycles in the PCR for the given application (starting material, target, primer). SNP Pol PCR with cell lysates Animal cells and E.coli can be used directly for PCR with the SNP Pol DNA polymerase! No separate lysis or proteinase K digestion is necessary. PCR procedure:1. 50 - 500 cells are required per PCR batch! 2. prepare PCR mix with primers and buffer and place on ice! 3. add the picked colony directly to 10-20µL water (no separate lysis and no proteinase K digestion), vortex briefly (5 seconds), then add this cell suspension directly to the PCR reaction mixture, e.g. 10µL cell suspension for a PCR preparation with a total volume of 20µL. An initial denaturation time of 2-3 minutes is sufficient is sufficient, can be extended to 5 minutes if necessary. Genomic DNA per reaction max. 100 copies is relatively low, but should still work. The remainder of this cell suspension can also be frozen away in order to carry out further tests. Optional: 4. if possible: do real-time PCR!The SNP Pol DNA polymerase (M3009 > or M3061 >) can be used together with non-specific fluorescent dyes (eg Genaxxon's Green DNA Dye > or SybrGreen®) in real-time PCR. When working with specific PCR probes, only the SNP PolTaq DNA polymerase can be used, since only these have a 5'-3 'exonuclease activity. With our high quality dNTPs as Set (M3015.4100) > or Mix (M3016.1010) > or our DNALadders > and our favourable standard agarose (M3044) > we can offer additional products for your PCR. Application areas for SNP Pol DNA and SNP PolTaq DNA polymerase- Monitoring, verification and detection of point mutations- Identification of correct or wrong CRISPR/Cas9 products- Verification/validation of sequencing results- Quantification of mutations (e.g. NGS results)- SNP-detection by allele-specific amplification (ASA) / Allele-specific PCR- Methylation specific PCRs (MSP) after bisulfite treated DNA (CpG methylation sides)- HLA genotyping- micro sequencing- realtime PCR with hydrolysis probes- realtime multiplex PCRs - DamID-seq data in C. elegans. As an alternative to ChIP, DNA adenine methyltransferase identification by sequencing (DamID-seq) was recently shown to be able to characterize binding sites in single mammalian cells. Additionally, DamID can be achieved for cell-type specific analysis by expressing Dam fusion proteins under tissue specific promoters in a controlled manner. In this report, we present a user-friendly pipeline to analyse DamID-seq data in C. elegans. Sharma R, Ritler D, Meister P.Tools for DNA adenine methyltransferase identification analysis of nuclear organization during C. elegans development. Genesis. 2016 Feb 4. doi: 10.1002/dvg.22925. - Minisequencing SNP genotyping with SNPase DNA Polymerase can be carried out by the procedure described in: Lovmar L, Fredriksson M, Liljedahl U, Sigurdsson S, Syvänen AC. Quantitative evaluation by minisequencing and microarrays reveals accurate multiplexed SNP genotyping of whole genome amplified DNA. Nucleic Acids Res. 2003;31:e129. - Allel specific mismatch selectivity by the HiDi DNA polymerase Drum M, Kranaster R, Ewald C, Blasczyk R, Marx A (2014) Variants of a Thermus aquaticus DNA Polymerase with Increased Selectivity for Applications in Allele- and Methylation-Specific Amplification. PLoS ONE 9(5): e96640. doi:10.1371/journal.pone.0096640

Genaxxon’s FAST DNA polymerase (2X) MasterMix with dye is the master mix of our FAST DNA polymerase (M3285) which is a robust enzyme, ideally suited for applications like genotyping and screening, amplifying with extreme speed of up to 2 seconds per 1kb, as well as high yield and consistency. FAST DNA polymerase has 5’-3’ exonuclease activity, but no 3’-5’ exonuclease (proofreading) activity. PCR products generated with this enzyme are A-tailed and can thus be cloned into TA cloning vectors. The extreme speed of Genaxxon’s FAST DNA polymerase allows the use of an extension rate of 4-8 kb/min. Genaxxon bioscience’s FAST DNA Polymerase (2X) MasterMix with dye includes all components needed for a fast PCR, except the primers. Besides this, it includes an inert red tracking dye for gel electrophoresis. Therefore, upon completion of the PCR, the reaction is ready for direct loading onto an agarose gel without the need of adding an additional loading buffer.Example of a typical PCR protocol (graphical presentation)* Ta is the annealing temperature (Ta should be 2°C above Tm**)  ** Tm is the melting temperature of a primer which is defined as the temperature at which 50% of the primer bind to the complementary sequence of the target DNA. Please note: By increasing Ta above Tm, this percentage decreases, however, primers will still anneal up to a certain degree and initiate extension. Therefore, PCR would still work with a Ta of several degrees higher than the Tm but with a dramatically reduced efficiency. Hence, we recommend optimizing the Ta by performing a temperature gradient (e.g., starting at the lowest Tm or a few degrees below and increasing with 2°C increments). *** Largest tested amplicon size: 5kb. Please note that longer extension times may be required for targets larger than 5kb!

Genaxxon’s FAST HotStart DNA polymerase (2X) MasterMix with dye is the master mix of our FAST HotStart DNA polymerase (M3287) which is a robust enzyme, ideally suited for applications like genotyping and screening, amplifying with extreme speed of up to 2 seconds per 1kb, as well as high yield and consistency.PCR products generated with this enzyme are A-tailed and can thus be cloned into TA cloning vectors. The extreme speed of Genaxxon’s FAST HotStart DNA polymerase allows the use of an extension rate of 4-8 kb/min. The buffer composition has been optimized via high-throughput screening and makes the enzyme particularly resistant to PCR inhibitors. Due to its robustness, Genaxxon’s FAST HotStart DNA polymerase (2X) MasterMix with dye is suitable for direct PCR from unpurified samples, including blood, urine, and bacterial colonies, making it the ideal choice for consistent results in fast complex PCR amplifications. Besides this, it includes an inert red tracking dye for gel electrophoresis. Therefore, upon completion of the PCR, the reaction is ready for direct loading onto an agarose gel without the need of adding an additional loading buffer.Example of a typical PCR protocol (graphical presentation)* Ta is the annealing temperature (Ta should be 2°C above Tm**)  ** Tm is the melting temperature of a primer which is defined as the temperature at which 50% of the primer bind to the complementary sequence of the target DNA. Please note: By increasing Ta above Tm, this percentage decreases, however, primers will still anneal up to a certain degree and initiate extension. Therefore, PCR would still work with a Ta of several degrees higher than the Tm but with a dramatically reduced efficiency. Hence, we recommend optimizing the Ta by performing a temperature gradient (e.g., starting at the lowest Tm or a few degrees below and increasing with 2°C increments). *** Largest tested amplicon size: 5kb. Please note that longer extension times may be required for targets larger than 5kb!

Description Taq DNA Polymerase 1.1x Master Mix is a ready-to-use 1.1x reaction mix with the Ampliqon Taq DNA polymerase, the NH4+ buffer system, dNTPs and magnesium chloride present. A 50µL PCR reaction requires 45µL of the 1.1x Master Mix. Simply add primers, template and water to a total reaction volume of 50µL to successfully carry out primer extensions and other molecular biology applications. Taq DNA Polymerase 1.1x Master Mix offers several advantages. Set up time is significantly reduced. The chance of contaminating component stocks is eliminated. Reduction of reagent handling steps leads to better reproducibility. Standard tests can be set up with the confidence that results will be consistent every time. You can find more of our PCR master mixes here. Use also our agaroses and DNA ladders which are ideal for subsequent electrophoresis and PCR evaluation.

Taq OptiMix CLEAR is an optimised format of Taq DNA Polymerase Master Mix and is therefore a good alternative to Taq DNA Polymerase and Taq DNA Polymerase Master Mix. Taq OptiMix CLEAR ensures the user an increased specificity and improved PCR performance, even on difficult templates. Taq OptiMix CLEAR offers reduced set-up time and eliminates the risk of contamination of reaction components. Taq OptiMix CLEAR is suitable for standard PCR applications, screening and high throughput testing. Taq OptiMix CLEAR is an further improved version of the already existing ready-to-use 2x master mix with the Ampliqon Taq DNA polymerase, the NH4+ buffer system, dNTPs and magnesium chloride present. Each reaction requires 25µL of the Taq OptiMix CLEAR. Simply add primers, template and water to a total reaction volume of 50µL to successfully carry out primer extensions and other molecular biology applications. Taq OptiMix CLEAR offers several advantages: - Reduced set up time and risk of contamination. - Fewer reagent handling steps- resulting in higher reproducibility. - Optimized for specificity. Composition of the Taq OptiMix CLEAR (2x) Tris-HCl pH8.5, (NH4)2S04, 3mM MgCl2, 0.2% Tween®20 0.4mM of each dNTP 0.08 units/µL Ampliqon Taq DNA polymerase Recommended Storage and Stability:Long term storage at -20 °C. Product expiry at -20 °C is stated on the label. Quality Control:Taq DNA Polymerase is tested for contaminating activities, with no traces of endonuclease activity, nicking activity or exonuclease activity. Unit Definition:One unit is defined as the amount of polymerase that incorporates 10 nmoles of dNTPs into acid-precipitable DNA in 30 minutes at 72 °C under standard assay conditions. Weitere PCR-Mastermixe von Genaxxon und Ampliqon finden Sie hier. Unsere Agarosen und DNA Marker sind ideal für die nachfolgende Elektrophorese geeignet.

Description Taq DNA Polymerase 1.1x Master Mix RED is a ready-to-use 1.1x reaction mix with the Ampliqon Taq DNA polymerase, the NH4+ buffer system, dNTPs and magnesium chloride present. Each reaction requires 45μL of the 1.1x Master Mix RED. Simply add primers, template and water to a total reaction volume of 50μL to successfully carry out primer extensions and other molecular biology applications. Taq DNA Polymerase 1.1x Master Mix RED offers several advantages. Setup time is significantly reduced. The chance of contaminating  component stock is eliminated.   Reduction of reagent handling steps leads to better reproducibility. Standard tests can be setup with the confidence that results will be consistent every time. There is no need to buy and use separate loading dyes. Simply load a portion of the PCR reaction product on to an agarose gel for electrophoresis and subsequent visualization. The red dye front runs at 1000 to 2000 bp on a 0.5 to 1.5% agarose gel. Unsere Agarosen und DNA Marker sind ideal für die nachfolgende Elektrophorese geeignet.

Taq DNA Polymerase Master Mix Red is a good alternative to Taq DNA Polymerase Master Mix with the same advantages. The inert red dye and a stabilizer are extra features, which allow direct loading onto your agarose gel for analysis. Features     No need for separate loading dye    Taq DNA Polymerase Master Mix Red is ready-made for electrophoresis and visualization    Fewer handling steps Description Taq DNA Polymerase Master Mix Red is a ready to use as a 2x reaction mix. Taq DNA Polymerase Master Mix Red is available in two final MgCl2 concentrations: 1.5mM and 2.0mM. Taq DNA Polymerase Master Mix Red is composed of Ampliqon Taq DNA Polymerase, the NH4+ buffer system, dNTPs and magnesium chloride.  Unsere Agarosen und DNA Marker sind ideal für die nachfolgende Elektrophorese geeignet.

Die High-quality Taq DNA Polymerase S für hohe Selektivität von 100 bp bis 10 kb ist eine hochprozessive 5' - 3' DNA Polymerase ohne 3' - 5' Exonukleaseaktivität. Der Puffer ist für eine hohe Selektivität bei der Amplifikation optimiert. Die hohe Prozessivität der Genaxxon Taq-Polymerase erlaubt die Amplifikation von DNA-Fragmenten bis zu 10 kBasen. Die Polymerase wird mit 10fach Puffer und separatem MgCl2 geliefert. Der mitgelieferte 'complete buffer' enthält 15mM MgCl2. Have a look on our Agaroses and DNA Marker. They are ideal for subsequent electrophoresis.

TEMPase Hot Start Master Mix is the popular alternative to TEMPase Hot Start DNA Polymerase. It offers the same excellent performance and increased reproducibility and additionoally the advantage of a ready-to-use 2-time PCR master mix. FEATURES - Minimal optimisation- Convenient reaction set up at room temperature- Time-saving premixed solution- Increased sensitivity, specificity and product yield- Consistent test results- Lower risk of contamination DESCRIPTION Ampliqon TEMPase Hot Start DNA Polymerase 2x Master Mix is a ready to use master mix composed of TEMPase Hot Start DNA Polymerase, dNTPs, MgCl2 and either TEMPase Buffer C (a balanced KCI/(NH4)2 SO4 Tris buffer system) or TEMPase Buffer A (a (NH4)2 SO4 tris buffer system). The TEMPase buffer system covers all needs for PCR applications and allow the user to choose the optimal buffer for specific PCR set-ups and applications. TIP - CHOOSE THE RIGHT TEMPASE HOT START MASTER MIX For most standard applications Master Mix A based on Ammonium Buffer is the best option. It promotes robust amplification, high yield and high specificity. In certain cases, Master Mix C is the best option. Please check also our SuperHot Hot Start Mastermix with or without tracking dye. 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.

Direct PCR amplification from plant parts (leaves, stem, roots) without the need for prior DNA isolation or DNA purification! The Genaxxon bioscience IdentityPlant 2X Mastermix contains an optimized polymerase that is highly resistant to PCR inhibitors. This master mix is delivered with lysis buffer. Advantages:- The polymerase that is used in our IdentityPlant master mix has been specifically optimized to tolerate a variety of PCR inhibitors that otherwise prevent direct PCR from plant.- The IdentityPlant 2X master mix ensures reproducible results, and significantly reduces set-up times and the risk of pipetting errors. NOTE: Due to the use of the specifically engineered Hotstart DNA polymerase and the specific buffer used for the IdentityPlant 2X PCR master mix the use of protocols typically already established in the laboratory is highly likely to result in reaction failure as buffer compositions are different from that used before. Additional PCR master mixes can be found here: qPCR/realtime master mixes > and Standard PCR master mixes >.

Direct PCR amplification of meat-or milk-specific DNA sequences from prepared food containing beef, pork, lamb, poultry or turkey, without the need for prior DNA isolation or DNA purification! The Genaxxon bioscience IdentityTaq 2X Mastermix contains an optimized polymerase that is highly resistant to PCR inhibitors. Fatty samples, such as e.g. Salami, cheese or sausage can be analyzed directly and without prior processing. Other problematic samples, such as wild animal hair or saliva, can thus be easily examined. This master mix is delivered without lysis buffer. If you need the IdentityTaq PCR 2X master mix with lysis buffer, please refer to the M3089 >. Advantages:- The IdentityTaq polymerase that is used in our IdentityTaq master mix has been specifically optimized to tolerate a variety of PCR inhibitors that otherwise prevent direct PCR from cell extracts.- The IdentityTaq 2X master mix ensures reproducible results, and significantly reduces set-up times and the risk of pipetting errors. NOTE: Due to the use of the specifically engineered Hotstart DNA polymerase and the specific buffer used for the IdentityTaq 2X PCR master mix the use of protocols typically already established in the laboratory is highly likely to result in reaction failure as buffer compositions are different from that used before. Additional PCR master mixes can be found here: qPCR/realtime master mixes > and Standard PCR master mixes >.

Direct PCR amplification of meat-or milk-specific DNA sequences from prepared food containing beef, pork, lamb, poultry or turkey, without the need for prior DNA isolation or DNA purification! The Genaxxon bioscience IdentityTaq 2X Mastermix enables PCR amplification of meat-specific or milk-specific DNA target sequences from liquid or solid food, prepared for human or animal consumption, like Hamburgers, hot dogs, doner kebabs, lasagne or other products that contain (should contain) meat or milk products. It requires only a short and easy pre-PCR lysis step without the need for prior DNA isolation and purification. The food can be raw or cooked, non-refrigerated, chilled or frozen. Simply take a 50mg - 100mg sample of food containing the meat and add 200μL lysis buffer. After the lysis step, the PCR can be started immediately. The IdentityTaq 2X master mix ensures reproducible results and significantly reduces set-up times and the risk of pipetting errors. The IdentityTaq polymerase, which is used in our IdentityTaq master mix, has been specifically optimized to tolerate a variety of PCR inhibitors that otherwise prevent direct PCR from cell extracts. NOTE: The accompanying protocol was developed for specific use with the engineered HotStart DNA polymerase, and the buffer contained in the IdentityTaq 2X PCR Master Mix. Due to the use of the specifically engineered HotStart DNA polymerase and the specific buffer used for the IdentityTaq 2X PCR Master Mix, the use of protocols typically already established in the laboratory is highly likely to result in reaction failure as buffer compositions are different from that used before. The proprietary lysis buffer is different from that routinely used with Proteinase K, for tissue digestion and subsequent PCR, and the annealing temperatures required for subsequent PCR are also likely to be different. Additional PCR master mixes can be found here: qPCR/realtime master mixes > and Standard PCR master mixes >.

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. While using our LyoBalls there is no need for cooling anymore! The lyoophilized master mix is stable at ambient temperature for at least 24 months if unopened! Our Hotstart Polymerase guarantees that the enzyme is not active during setup and below 55°C at all PCR cycles. Thus 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. 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. Each bead is equivalent to one 20µL PCR reaction.The lyophilized master mix in an 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-use Our lyophilized qPCR Probe master mix is also available in powder form (LyoMix, M3071 >). With our high quality dNTPs as Set > or Mix > or our DNA Ladders > and our favourable standard agarose (M3044 >) we can offer additional products for your PCR.

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. No cooling/cooling chain necessary! The beads and all ingredients are unopened stable at ambient temperature for at least 24 months! While using our LyoBalls there is no need for cooling anymore! The lyoophilized master mix is stable at ambient temperature for at least 24 months if unopened! Our Hotstart Polymerase guarantees that the enzyme is not active during setup and below 55°C at all PCR cycles. Thus 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. 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. Each bead is equivalent to one 20µL PCR reaction.The lyophilized master mix in an 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-use Our lyophilized qPCR Probe master mix is also available in powder form (LyoMix, M3071 >). With our high quality dNTPs as Set > or Mix > or our DNA Ladders > and our favourable standard agarose (M3044 >) we can offer additional products for your PCR.