VIRAL RNA EXTRACTION FOR COVID-19

Ensuring Sample Preparation Excellence

From nucleic acid integrity and purification to genomic insights

Preserve sample integrity from the start- Our 510(k) cleared,
Guanidine free stabilization reagent technologies ensure nucleic acid integrity for reliable downstream results.

High-yield, high-purity DNA/RNA with ease. Our magnetic
bead-based reagent solutions provide superior recovery and quality for downstream success.

Better Sample, Better Data!
High-quality sample preparation reagents are essential for accurate sequencing. MagBio’s long-read sequencing (patent pending) and short-read sample preparation reagents reduce sequencing errors and bias, leading to reliable data.

Our paramagnetic bead-based sample preparation technologies support molecular diagnostics, pathogen surveillance, and infectious disease research by delivering consistent nucleic acid recovery, workflow compatibility, and scalable supply for reliable, high-performance detection workflows.

Featured Products

HighPrep PCR

Magnetic bead-based reagent for manual and automated post-PCR and post-enzymatic reaction cleanup, NGS library cleanup, and reliable DNA size selection.

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HighPrep Viral DNA & RNA Kit

Magnetic bead based kit optimized for extraction of RNA from a variety of viral samples - Swabs, whole blood, serum, plasma, saliva & other body fluids.

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HighPrep RNA Elite

Magnetic beads based reagent for manual and automated clean-up or concentration of RNA and single-stranded cDNA after enzymatic reactions or prior sequencing.

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MagBio offers free samples of all kits & reagents for testing so that you can validate our products and ensure they suit your workflow before committing to any purchases.

Click on the link below or give us a call at (301) 302-0144 to request your free sample today!

Request A Sample Kit

News and Blogs

June 26, 2026

What Laboratories Should Evaluate When Considering Alternatives to the MagMAX™ Viral/Pathogen Ultra Nucleic Acid Isolation Kit

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June 19, 2026

Simplify Multi-Pathogen Extraction Workflows with the HighPrep Viral-Pathogen DNA & RNA Kit

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July 21, 2025

Magnetic Bead DNA Cleanup Protocols: Optimizing PCR Cleanups with HighPrep vs. Spin Columns

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HighPrep PCR

Direct and Cost-effective Alternative to the Leading SPRI Bead-Based Reagent

Paramagnetic bead-based post PCR clean-up reagent designed for efficient DNA purification, tight DNA size selection, NGS library clean-up, and Oxford Nanopore Technologies® (ONT) Library Preparation Cleanup. With no centrifugation or filtration required, it enables a simple, scalable workflow for both manual and fully automated sample processing.

NYU GenCore Comparison: HighPrep PCR Beads as an AMPureXP Alternative

 Performance Data  |  Comparative Data  |  Request a Quote 


Grouped product items
Cat.# Product Name Price Qty
AC-60005 HighPrep PCR (5 mL)
$133.05
AC-60050 HighPrep PCR (50 mL)
$687.43
AC-60250 HighPrep PCR (250 mL)
$2,817.65
AC-60500 HighPrep PCR (500 mL)
$4,577.81
AC-60005E HighPrep PCR - DX (5 mL)
$133.05
AC-60050E HighPrep PCR - DX (50 mL)
$687.43
AC-60250E HighPrep PCR - DX (250 mL)
$2,817.65
AC-60500E HighPrep PCR - DX (500 mL)
$4,577.81
Applications

Post-PCR and post-enzymatic reaction clean-up used for/during:

  • NGS library preparation
  • DNA size selection for NGS
  • Microarrays
  • PCR
  • Restriction enzyme digestions, adapter ligations
  • Cloning

Benefits

  • Rapid and reliable post-PCR and DNA clean-up reagent
  • Achieve uniform and consistent DNA fragments
  • High recovery of amplicons >100 bp
  • Uniform fragments size distribution
  • Adaptable to high throughput liquid handling workstations

  • What is HighPrep PCR used for?
    A paramagnetic bead-based reagent for post-PCR clean-up, NGS library clean-up, Oxford Nanopore Technologies® (ONT) library preparation and DNA size selection. The purified DNA is ready for downstream applications, such as sequencing, qPCR, cloning, microarrays and more.
  • Does it need a centrifuge or spin columns?
    No. It uses a magnetic bead-based workflow with an ethanol wash; no centrifugation or filtration is required. So, it’s faster, uses fewer consumables, and adapts easily to automation.
  • What DNA recovery and fragment size can I expect?
    Expect >70% DNA recovery. At a 1.8x bead ratio, the reagent provides reliable recovery of DNA fragments ≥100 bp. Adjusting the bead-to-sample ratio shifts the cut-off for precise DNA size selection.
  • Can I use it for NGS library prep and size selection?
    Yes. It’s designed for NGS library cleanup and tunable DNA size selection, giving uniform, consistent fragment distribution for sequencing workflows.
  • Is it compatible with automated liquid handlers?
    Yes. It’s adaptable to most nucleic-acid purification instruments, and a ready-made KingFisher™ Flex script is available on request; reducing hands-on time and pipetting error.
  • What sample types and inputs does it work with?
    It works with DNA, PCR products, cDNA and genomic DNA (gDNA), with scalable starting amounts. It removes salts, primers, primer-dimers and unincorporated dNTPs.
  • What’s the difference between HighPrep PCR and HighPrep PCR-DX product categories?
    The HighPrep PCR - DX product category is the regulatory-registered CE-IVD grade for diagnostic workflows and the HighPrep PCR product category is for Research Use Only (RUO).
  • Is it suitable for clinical and diagnostic labs?
    The HighPrep PCR - DX product category is CE-IVD registered and is suitable for clinical and diagnostic labs.
  • Can I try it before buying?
    Yes, you may request a free sample to validate it in your workflow first.
  • How should it be stored, and what is the shelf life?
    It’s stable for 18 months when stored at 2-8°C. DO NOT FREEZE.

HighPrep PCR is a paramagnetic beads-based post PCR clean-up reagent designed for efficient purification of amplicons and tight size-specific selection of DNA fragments. The purification consists of removal of salts, primers, primer-dimers, dNTPs, as DNA fragments are selectively bound to the magnetic bead particles. Highly purified DNA is eluted with low salt elution buffer or water which can be used directly for downstream applications, such as library construction, next generation sequencing (NGS), Sanger sequencing, cloning, restriction digestions, adapter ligation, microarrays, and so on. This protocol can be used for manual procedures as well as in automation. 

Efficient recovery of amplicons achieved with HighPrep™ PCR Clean-up System

REGULATORY
Product information area

This is a short overview of the protocol, for all detailed protocols, please refer to PRODUCT DOCUMENTS

1
2
3
4
5

Add reagent

Add HighPrep PCR to the reaction mixture

Bind

Bind DNA to paramagnetic beads

Separate

Separate beads and DNA from contaminants

Wash

Wash beads with 80% ethanol to remove contaminants

Elute

Elute purified PCR products or other DNA fragments from beads

1

Add reagent

Add HighPrep PCR to the reaction mixture

2

Bind

Bind DNA to paramagnetic beads

3

Separate

Separate beads and DNA from contaminants

4

Wash

Wash beads with 80% ethanol to remove contaminants

5

Elute

Elute purified PCR products or other DNA fragments from beads

FeaturesSpecifications
Main function

Purifies DNA and amplicons for next generation sequencing (NGS) and other applications. Selectively binds fragments ≥100 bp depending on sample to bead ratio, and performs size selection by changing the bead ratio.

Starting material
(Sample matrix)

DNA, PCR products, cDNA, gDNA
Starting amount Scalable
DNA recovery >70%
Process method Manual or automated
Instrument

Adaptable to most nucleic acid purification instruments, but a ready-made script for KingFisher Flex is available upon request.

Downstream-ready

Real time quantitative PCR (qPCR)/PCR, next generation sequencing (NGS), Sanger sequencing, cloning, restriction digestions, microarrays, etc.

Elution volume 15 µl or above
Purification method Magnetic bead-based technology
Storage temperature Store at 2-8°C. DO NOT FREEZE
Shelf life Stable for 18 months when stored at 2-8°C.

Trusted in Published Genomics Research

HighPrep PCR is trusted by private and academic institutions worldwide and has been cited in over 6,000 publications. Selected references are listed below.

  1. Lars Velten, Simon Anders, Aleksandra Pekowska, Aino I Järvelin, Wolfgang Huber, Vicent Pelechano and Lars M Steinmetz
  2. Divya Bhanu, Kandasamy Ulaganathan, Arun K. Shanker and S. Desai
  3. Anna-Karin Bergl, Clara Navarrete, Martin K. M. Engqvist, Emily Hoberg, Zsolt Szilagyi, Robert W. Taylor, Claes, M. Gustafsson, Maria Falkenberg, Anders R. Clausen
  4. Rajendran Mathan Kumar, Gurwinder Kaur, Anand Kumar, Monu Bala, Nitin Kumar Singh, Navjot Kaur, Narender Kumar and Shanmugam Mayilraj
  5. Ramesan Girish Nair, Gurwinder Kaur, Indu Khatri, Nitin Kumar Singh, Sudeep Kumar Maurya, Srikrishna Subramanian, Arunanshu Behera, Divya Dahiya, Javed N Agrewala and Shanmugam Mayilraj
  6. Martin Frederik Laursen, Gitte Zachariassen, Martin Iain Bahl, Anders Bergström, Arne Høst, Kim F. Michaelsen and Tine Rask Licht
  7. Martin Frederik Laursen, Louise B. B. Andersen, Kim F. Michaelsen, Christian Mølgaard, Ellen Trolle, Martin Iain Bahl, Tine Rask Licht.
  8. Awanti Sambarey, Abhinandan Devaprasad, Abhilash Mohan, Asma Ahmed, Soumya Nayak, Soumya Swaminathan, George D'Souza, Anto Jesuraj, Chirag Dhar, Subash Babu, Annapurna Vykarnam, Nagasuma Chandra
  9. Tiffany Leidy-Davis, Kai Cheng, Leslie O. Goodwin, Judith L. Morgan, Wen Chun Juan, Xavier Roca, Sin-Tiong Ong, David E. Bergstrom
  10. Erick Strauss, Cynthia Kinsland, Ying Ge, Fred W. McLafferty, and Tadhg P. Begley
  11. Franz Hölker, Christian Wurzbacher, Carsten Weißenborn, Michael T. Monaghan, Stephanie I. J. Holzhauer, Katrin Premke
  12. De Tender, Lisa I. Devriese, Annelies Haegeman, Sara Maes, Tom Ruttink, and Peter Dawyndt
  13. Rajendran Mathan Kumar, Gurwinder Kaur, Narender Kumar, Anand Kumar, Nitin Kumar Singh, Monu Bala, Navjot Kaur, Shanmugam Mayilraj
  14. Rajendran Mathan Kumar, Gurwinder Kaur, Narender Kumar, Anand Kumar, Nitin Kumar Singh, Monu Bala, Navjot Kaur and Shanmugam Mayilraj.
  15. Anders R Clausen, Scott A Lujan, Adam B Burkholder, Clinton D Orebaugh, Jessica S Williams, Maryam F Clausen, Ewa P Malc, Piotr A Mieczkowski, David C Fargo, Duncan J Smith & Thomas A Kunkel
  16. Sujay Paul, Yolanda Cortez, Nadia Vera, Gretty K. Villena, Marcel Gutiérrez-Correa
  17. Yesupatham Sathishkumar, Chandran Krishnaraj, Kalyanaraman Rajagopa, Dwaipayan Sen and Yang Soo Lee
  18. Peer H. A. Timmers, H. C. A. Widjaja-Greefkes, Javier Ramiro-Garcia, Caroline M. Plugge and Alfons J. M. Stams
  19. Adriaan A. van Beek, Floor Hugenholtz, Ben Meijer, Bruno Sovran, Olaf Perdijk, Wilbert P. Vermeij, Renata M. C. Brandt, Sander Barnhoorn, Jan H. J. Hoeijmakers, Paul de Vos, Pieter J. M. Leenen, Rudi W. Hendriks and Huub F. J. Savelkoul.
  20. Martin Frederik Laursen, Louise B. B. Andersen, Kim F. Michaelsen, Christian Mølgaard, Ellen Trolle, Martin Iain Bahl, Tine Rask Licht
  21. Karen A. Cameron, Marek Stibal, Jakub D. Zarsky, Erkin Gozdereliler, Morten Schostag and Carsten S. Jacobsen
  22. Mounir, Z., J. M. Korn, T. Westerling, F. Lin, C. A. Kirby, M. Schirle, G. McAllister
  23. Fransen, Floris; Sahasrabudhe, Neha; Elderman, Marlies; Bosveld, Margaret; El Aidy, Sahar Farouk Abdelsalam; Hugenholtz, Floor; Borghuis, Theo; Kousemaker, Ben; Winkel, Simon; van der Gaast-de Jongh
  24. Marcelle J. van der Waals, Siavash Atashgahi, Ulisses Nunes da Rocha, Bas M. van der Zaan, Hauke Smidt, Jan Gerritse
  25. Rajendran Mathan Kumar, Gurwinder Kaur, Narender Kumar, Anand Kumar, Nitin Kumar Singh, Monu Bala, Navjot Kaur, Shanmugam Mayilraj

Want to share one more reference? Write us an email.