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Viral DNA/RNA Co-Extraction Kits for Multiplex Pathogen Detection

 

Viral DNA/RNA co-extraction kits simultaneously purify viral DNA and RNA from plasma, serum, nasopharyngeal swabs, urine, saliva, CSF, and fecal samples using a single chaotropic lysis buffer that disrupts viral envelopes and capsids and releases nucleic acids for silica-column or magnetic bead purification. 

MBP carries Zymo Research Quick-DNA/RNA Viral kits validated for 10+ virus families, supporting multiplex pathogen detection, RT-qPCR, viral surveillance, and pan-pathogen next-generation sequencing workflows by contacting customerservice@mbpinc.net.

Viral DNA/RNA

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MV Total RNA Isolation
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USD192.08 - USD708.29
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Magbio HighPrep Viral DNA & RNA Kit
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Magbio HighPrep Viral-Bacterial DNA & RNA Kit
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Magbio HighPrep Viral-Pathogen DNA & RNA Kit
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Quick-DNA/RNA Viral 96 Kit
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USD683.62 - USD1,212.96
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USD488.30 - USD866.40
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Quick-DNA/RNA Viral MagBead
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USD468.16 - USD1,709.05
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USD334.40 - USD1,220.75
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Quick-DNA/RNA™ Viral Kit
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USD94.43 - USD875.14
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Virus RNA Kit
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What are Viral DNA/RNA Co-Extraction Kits?

 

Viral DNA/RNA co-extraction kits simultaneously purify both viral DNA and viral RNA from cell-free biological samples -  plasma, serum, urine, nasopharyngeal swabs, saliva, cerebrospinal fluid, cell culture media, blood, and fecal samples - using a single chaotropic lysis buffer that disrupts viral envelopes and capsids and releases nucleic acids for binding to silica-membrane columns or paramagnetic beads. Unlike RNA-only viral kits that miss ssDNA viruses (parvovirus, adeno-associated virus) and dsDNA viruses (adenovirus, herpesvirus, CMV, EBV), viral DNA/RNA co-extraction formats recover all viral genome types from the same input volume - enabling pan-pathogen multiplex RT-qPCR and metagenomic NGS panels that cover both RNA and DNA viral targets simultaneously. Use a viral DNA/RNA co-extraction kit -- not an RNA-only viral kit - whenever your assay panel includes any DNA virus target alongside RNA virus targets, or whenever metagenomic NGS of a clinical sample is the downstream application.

 

What you will find:

 

  • Spin-Column Extraction: Dependable, standalone preparation kits tailored for quick isolation with minimal sequence bias, perfect for specialized low-volume processing.

  • 96-Well Plate Systems: Designed for efficient parallel processing, these kits enable high-throughput screening while maintaining both yield and purity.

  • Mag Beads Technology: Automated bead-based systems for efficient recovery of viral and bacterial DNA/RNA, providing consistently reproducible results through rigorous testing.

 

How to Choose a Viral DNA/RNA Co-Extraction Kit

 

Format: Spin-Column vs. 96-Well Plate vs. Magnetic Bead

The Zymo Quick-DNA/RNA Viral Kit (spin-column, 1-50 samples) completes extraction in approximately 20 minutes per batch using a microcentrifuge - the fastest format for low-volume clinical or diagnostic workflows. The Quick-DNA/RNA Viral 96 Kit processes up to 96 samples per run on a 96-well spin plate with centrifuge or vacuum manifold. The Quick-DNA/RNA Viral MagBead Kit processes 96 samples on automation platforms (KingFisher, Tecan, Hamilton) with no centrifugation during purification. Match the format to daily sample volume and available equipment.

Single-Buffer vs. Multi-Step Lysis

Zymo viral kits use a single lysis buffer that simultaneously lyses viral particles and conditions nucleic acids for column or bead binding - eliminating protease pre-treatment and reducing hands-on steps. QIAGEN QIAamp Viral RNA Mini Kit uses a two-step approach (AVL buffer + ethanol); Thermo Fisher PureLink Viral RNA/DNA Mini Kit uses a similar multi-buffer approach. Single-buffer formats reduce pipetting steps and errors in high-throughput batch processing.

DNA Shield Sample Compatibility

Swabs and samples stored in Zymo DNA/RNA Shield load directly into viral co-extraction workflows without additional neutralization or dilution steps. Confirm the kit's compatibility with the specific transport medium used (VTM, UTM, PBS, DNA/RNA Shield, Norgen NAP) before adopting it in a multi-site surveillance network.

Pan-Pathogen Scope

For pan-pathogen NGS panels that must detect RNA viruses, DNA viruses, bacteria, and parasites from the same clinical specimen, the Quick-DNA/RNA Viral MagBead Kit recovers viral DNA and RNA plus easily lysable bacterial DNA from the same sample, broadening panel coverage beyond viral-only targets.

Elution Volume and Sensitivity

For low-titer samples (viral load <1x10^3 copies/ml), elute in 30-50 ul to concentrate nucleic acids for sensitive RT-qPCR. For NGS applications requiring higher total nucleic acid mass, elute in 100 ul or pool two extractions from the same sample. Include a spike-in control (cel-miR-39 RNA + internal DNA spike) in every extraction batch to monitor efficiency and detect inhibitor carryover.

 

Specifications Context

 

Key performance benchmarks: >=70% nucleic acid recovery from spike-in controls, eluted DNA/RNA with A260/A280 >= 1.7, and RT-qPCR Ct within 2 cycles of reference extraction for both RNA and DNA viral targets. The Zymo Quick-DNA/RNA Viral 96 Kit uses a single buffer system validated for enteroviruses, rhinoviruses, coronaviruses, HIV, HCV, influenza A, flaviviruses, measles, parainfluenza, and parvovirus, with nucleic acids eluted in DNase/RNase-free water suitable for RT-PCR, NGS, and hybridization. The Quick-DNA/RNA Viral MagBead Kit recovers small RNA (>50 nt) to large DNA (>200 kb) from the same binding event, covering the full viral genome-size spectrum in a single extraction. Viral DNA/RNA co-extraction is standard practice in multi-pathogen respiratory panel diagnostics and clinical metagenomics programs at institutions including MD Anderson Cancer Center and Vanderbilt University.

 

For bulk pricing on Quick-DNA/RNA Viral kits, format selection guidance for pan-pathogen panels, or multiplex RT-qPCR pairing recommendations, contact the MBP team

FAQ

Viral DNA/RNA co-extraction kits simultaneously purify both DNA and RNA from viruses present in cell-free biological samples — plasma, serum, urine, nasopharyngeal swabs, saliva, cerebrospinal fluid, cell culture media, and fecal samples — using a single chaotropic lysis buffer that disrupts viral envelopes and capsids and releases nucleic acids for binding to silica-membrane columns or paramagnetic beads. Unlike RNA-only viral kits, co-extraction formats recover both RNA viruses (influenza, SARS-CoV-2, HIV, HCV) and DNA viruses (herpesviruses, adenoviruses, HPV, parvovirus) from the same input volume.
Many diagnostic and surveillance panels include both RNA viruses (respiratory syncytial virus, influenza A/B, SARS-CoV-2, enteroviruses) and DNA viruses (adenovirus, CMV, EBV, HPV) in the same assay. Co-extracting DNA and RNA from a single 200 µl input sample eliminates the need to split limited clinical material between separate RNA and DNA extraction workflows, reduces processing time, and ensures both viral genome types are recovered from identical sample conditions — critical for multiplex RT-qPCR and pan-pathogen NGS panels.
The Zymo Research Quick-DNA/RNA Viral Kit has been validated for enteroviruses, rhinoviruses, coronaviruses (including SARS-CoV-2), HIV, hepatitis C virus (HCV), influenza A, flaviviruses (dengue, Zika), measles, parainfluenza, and parvovirus (a ssDNA virus). The MagBead format additionally covers bacterial pathogens and protozoa from swab and fecal samples stored in DNA/RNA Shield. Contact MBP for the full validated virus species list and protocol guidance for non-listed targets.
The Zymo Quick-DNA/RNA Viral Kit (spin-column format) accepts 50–200 µl of plasma, serum, urine, or swab eluate per extraction. The Quick-DNA/RNA Viral 96 Kit (96-well spin plate) accepts similar volumes in each well. The Quick-DNA/RNA Viral MagBead Kit processes samples from plasma, serum, urine, cell culture media, blood, saliva, cellular suspensions, biopsies, and swab and fecal samples stored in DNA/RNA Shield, with a standard 200 µl input per well in 96-well format.
The Zymo Research Quick-DNA/RNA Viral Kit series uses a specialized buffer system designed for complete viral particle lysis and efficient nucleic acid binding without requiring the user to add exogenous carrier RNA to the lysis buffer. The single-buffer lysis system eliminates the pre-extraction carrier RNA preparation step required by QIAGEN QIAamp Viral RNA Mini Kit, simplifying the workflow and reducing pipetting errors in high-throughput diagnostic batches.
Spin-column viral DNA/RNA kits elute into 30–100 µl of DNase/RNase-free water; eluting in 30–50 µl concentrates nucleic acids for sensitive RT-qPCR from low-titer samples. The Quick-DNA/RNA Viral MagBead Kit elutes small (>50 nt) and large (>200 kb) DNA and RNA from magnetic beads into a similar volume. For multiplex NGS libraries requiring more total nucleic acid mass, use 100 µl elution and pool replicate extractions from low-titer samples.
Yes. Viral DNA/RNA co-extraction kits that recover both viral DNA and RNA from the same input sample are the recommended format for pan-pathogen metagenomic NGS panels, which simultaneously detect RNA viruses, DNA viruses, bacteria, and protozoa from a single clinical specimen. The Quick-DNA/RNA Viral MagBead Kit is used in Zymo Research's SARS-CoV-2 workflow and has been applied to pan-respiratory-pathogen NGS panels covering influenza, SARS-CoV-2, RSV, adenovirus, and parainfluenza from the same nasopharyngeal swab input.
Samples intended for viral DNA/RNA co-extraction should be processed immediately or stabilized in Zymo DNA/RNA Shield, which simultaneously inactivates infectious agents (viruses, bacteria, protozoa), prevents nucleic acid degradation, and enables room-temperature sample storage and shipping for up to 30 days. Swabs in DNA/RNA Shield are directly loadable into viral extraction workflows. For plasma and serum, perform two-spin separation within 6 hours of blood collection before storage at -80°C in single-use aliquots.
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