Q5

Q5® High-Fidelity DNA Polymerases

 

Find the right Q5 product for your polymerase chain reaction (PCR)

 

What are the differences between the numerous Q5® Polymerase products available?

 

The five features of Q5 High-Fidelity DNA Polymerase

  1. Extremely low error rates
    At ~280X higher than Taq, Q5 offers unparalleled fidelity for your most important samples. For information on how fidelity affects PCR‑induced errors and experimental outcomes, explore the PCR Fidelity Estimator tool.

  2. Robust amplification with minimal optimization
    High specificity and yield are absolute requirements for today's molecular biology techniques.

  3. Superior coverage for a broad range of amplicons, regardless of GC content
    While other DNA polymerases can have difficulty amplifying high-GC or high-AT amplicons, Q5 displays superior performance for a wide range of templates.

Figure 1: Robust Amplification with Q5 and Q5 Hot Start High-Fidelity DNA Polymerases

Amplification performance of Q5® High-Fidelity DNA Polymerase as compared to other polymerases 
Amplification of a variety of human genomic amplicons from low to high GC content using either Q5 or Q5 Hot Start High-Fidelity DNA Polymerase. Reactions using Q5 Hot Start were set up at room temperature. All reactions were conducted using 30 cycles of amplification and visualized by microfluidic LabChip® analysis.

Figure 2: Q5 formats support robust amplification of a broad range of targets

Coverage diagram of Q5 High-Fidelity DNA Polymerases, with options for flexibility or convenience 
For flexibility, standalone Q5 polymerase products and the included High GC Enhancer can support amplification of targets with differing amounts of GC content. For convenience, and to amplify a broad range of target GC content, Q5 master mixes are recommended.

  1. Shorter PCR protocols
    Achieve precision without sacrificing speed. Q5's unique design incorporating the SSo7d processivity-enhancing domain enables shorter extension times, as low as 5 seconds per kb. Additionally, the aptamer-based hot start requires no initial denaturation step and enables room temperature setup.

    For added convenience, Q5 products are compatible with single (i.e., "universal") annealing temperature protocols. Please see our application note for more information: Universal Annealing Temperature in PCR and its Impact on Amplification Results.

  2. Amplify templates up to 30 kb
    When speed is a priority or DNA targets are long or complex, Q5‑XT provides a faster, more robust amplification solution while maintaining the performance you expect of Q5. Simple templates up to 30 kb and complex templates up to 20 kb can be amplified with high accuracy.
Figure 3: Q5-XT performs well on a broad range of DNA sizes

Comparison of various amplicon lengths for Q5-XT, as compared to other DNA polymerases 
PCR assays were performed on six targets with human genomic DNA, utilizing various hot start, high-fidelity PCR master mixes according to each manufacturer's recommended protocols. Ladder (L) is Quick-Load® 100 bp DNA Ladder (NEB #N0467). All PCR products were visualized by ethidium bromide staining on 1.2% TAE agarose gel.

 

 

Phusion™ DNA Polymerase was developed by Finnzymes Oy, now a part of Thermo Fisher Scientific.
THERMO SCIENTIFIC and PHUSION are registered trademarks and property of Thermo Fisher Scientific used under license.
ACCUPRIME and PLATINUM are trademarks of Thermo Fisher Scientific
PFUULTRA® and AGILENT are registered trademarks of Agilent Technologies, Inc.
MILLIPORE SIGMA® is a registered trademark of Merck KGAA
LABCHIP® is a registered trademark of Caliper Life Sciences, part of Perkin Elmer, Inc.

Q5® High-Fidelity DNA Polymerase sets a new standard for both fidelity and robust performance.

 


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Q5® High-Fidelity DNA Polymerases
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NEBNext® High-Fidelity 2X PCR Master Mix

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NEBNext® Q5® Hot Start HiFi PCR Master Mix

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NEBNext® Ultra™ II Q5® Master Mix

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NEBNext® Q5U® Master Mix

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Q5 Quick-Load High-Fidelity 2X Master Mix

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Q5 Quick-Load Hot Start High-Fidelity 2X Master Mix

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Q5® High-Fidelity 2X Master Mix

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Q5® High-Fidelity DNA Polymerase

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Q5® High-Fidelity PCR Kit

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Q5® Hot Start High-Fidelity 2X Master Mix

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Q5® Hot Start High-Fidelity DNA Polymerase

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Q5® Reaction Buffer Pack

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Q5® Blood Direct 2X Master Mix

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Q5®-XT Hot Start High-Fidelity 2X Master Mix

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Q5U® Hot Start High-Fidelity DNA Polymerase


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Protocols for Q5® High-Fidelity DNA Polymerases
Application Notes for Q5® High-Fidelity DNA Polymerases
    Publications related to Q5® High-Fidelity DNA Polymerases
    • Yafeng Li, Delu Song, Ying Song, Liangliang Zhao, Natalie Wolkow, John W Tobias, Wenchao Song, Joshua L Dunaief (2015) Iron-induced Local Complement Component 3 (C3) Up-regulation via Non-canonical Transforming Growth Factor (TGF)-β Signaling in the Retinal Pigment Epithelium. J Biol Chem; 290, 11918-34. PubMedID: 25802332, DOI: 10.1074/jbc.M115.645903
    • Yuan Xue, Jossef Osborn, Anand Panchal, Jay L Mellies (2015) The RpoE Stress Response Pathway Mediates Reduction of the Virulence of Enteropathogenic Escherichia coli by Zinc. Appl Environ Microbiol; 81, 3766-74. PubMedID: 25819956, DOI: 10.1128/AEM.00507-15
    • Longhai Dai, Can Liu, Yueming Zhu, Jiangsheng Zhang, Yan Men, Zeng Yan, Yuanxia Sun (2015) Functional Characterization of Cucurbitadienol Synthase and Triterpene Glycosyltransferase Involved in Biosynthesis of Mogrosides from Siraitia grosvenorii. Plant Cell Physiol; PubMedID: 25759326, DOI: 10.1093/pcp/pcv043
    • Harish Nag Kankipati, Marta Rubio-Texeira, Dries Castermans, George Diallinas, Johan M Thevelein (2015) Sul1 and Sul2 Sulfate Transceptors Signal to Protein Kinase A upon Exit of Sulfur Starvation. J Biol Chem; 290, 10430-46. PubMedID: 25724649, DOI: 10.1074/jbc.M114.629022
    • Amin Zargar, David N Quan, Milad Emamian, Chen Yu Tsao, Hsuan-Chen Wu, Chelsea R Virgile, William E Bentley (2015) Rational design of 'controller cells' to manipulate protein and phenotype expression. Metab Eng; PubMedID: 25908186, DOI: 10.1016/j.ymben.2015.04.001
    • Christine Henke, Pamela L Strissel, Maria-Theresa Schubert, Megan Mitchell, Claus C Stolt, Florian Faschingbauer, Matthias W Beckmann, Reiner Strick (2015) Selective expression of sense and antisense transcripts of the sushi-ichi-related retrotransposon - derived family during mouse placentogenesis. Retrovirology; 12, 9. PubMedID: 25888968, DOI: 10.1186/s12977-015-0138-8
    • Yonghe Zhang, Huiming Huang, Shanshan Xu, Bo Wang, Jianhua Ju, Huarong Tan, Wenli Li (2015) Activation and enhancement of Fredericamycin A production in deepsea-derived Streptomyces somaliensis SCSIO ZH66 by using ribosome engineering and response surface methodology. Microb Cell Fact; 14, 64. PubMedID: 25927229, DOI: 10.1186/s12934-015-0244-2
    • Binyamin D Berkovits, Christine Mayr (2015) Alternative 3' UTRs act as scaffolds to regulate membrane protein localization. Nature; PubMedID: 25896326, DOI: 10.1038/nature14321
    • Jun Wu, Daiji Okamura, Mo Li, Keiichiro Suzuki, Chongyuan Luo, Li Ma, Yupeng He, Zhongwei Li, Chris Benner, Isao Tamura, Marie N Krause, Joseph R Nery, Tingting Du, Zhuzhu Zhang, Tomoaki Hishida, Yuta Takahashi, Emi Aizawa, Na Young Kim, Jeronimo Lajara, Pedro Guillen, Josep M Campistol, Concepcion Rodriguez Esteban, Pablo J Ross, Alan Saghatelian, Bing Ren, Joseph R Ecker, Juan Carlos Izpisua Belmonte (2015) An alternative pluripotent state confers interspecies chimaeric competency. Nature; PubMedID: 25945737, DOI: 10.1038/nature14413
    • Bert De Rybel, Milad Adibi, Alice S. Breda, Jos R. Wendrich, Margot E. Smit, Ondej Novk, Nobutoshi Yamaguchi, Saiko Yoshida, Gert Van Isterdael, Joakim Palovaara, Bart Nijsse, Mark V. Boekschoten, Guido Hooiveld, Tom Beeckman, Doris Wagner, Karin Ljung, Christian Fleck, Dolf Weijers (2014) Integration of growth and patterning during vascular tissue formation in Arabidopsis Science; 345, 1255215. PubMedID: 25104393, DOI: 10.1126/science.1255215
    • Xin Duan, Arjun Krishnaswamy, Irina De la Huerta, Joshua R Sanes (2014) Type II Cadherins Guide Assembly of a Direction-Selective Retinal Circuit. Cell; 158, 793-807. PubMedID: 25126785, DOI: 10.1016/j.cell.2014.06.047
    • Martin Kostovcik, Craig C Bateman, Miroslav Kolarik, Lukasz L Stelinski, Bjarte H Jordal, Jiri Hulcr (2014) The ambrosia symbiosis is specific in some species and promiscuous in others: evidence from community pyrosequencing. ISME J; PubMedID: 25083930, DOI: 10.1038/ismej.2014.115
    • Connelly CM1, Porter LR2, TerMaat JR (2014) PCR amplification of a triple-repeat genetic target directly from whole blood in 15 minutes as a proof-of-principle PCR study for direct sample analysis for a clinically relevant target BMC Med Genet; 15, 130. PubMedID: 25495904, DOI: 10.1186/s12881-014-0130-5
    • Vidhyadhar Nandana, Sushant Singh, Abhay Narayan Singh, Vikash Kumar Dubey (2014) Procerain B, a cysteine protease from Calotropis procera, requires N-terminus pro-region for activity: cDNA cloning and expression with pro-sequence. Protein Expr Purif; 103C, 16-22. PubMedID: 25173974, DOI: 10.1016/j.pep.2014.08.003
    • Vladimir Potapov, Jennifer L. Ong. (2017) Examining Sources of Error in PCR by Single-Molecule Sequencing. PLOS One; PubMedID: 28683110
Comparison of High-Fidelity Polymerases
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Products and content are covered by one or more patents, trademarks and/or copyrights owned or controlled by New England Biolabs, Inc (NEB). The use of trademark symbols does not necessarily indicate that the name is trademarked in the country where it is being read; it indicates where the content was originally developed. All other trademarks are the property of their respective owners. The use of this product may require the buyer to obtain additional third-party intellectual property rights for certain applications. For more information, please email busdev@neb.com.

This product is intended for research purposes only. This product is not intended to be used for therapeutic or diagnostic purposes in humans or animals.

 


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