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Spin-Column Viral DNA/RNA Co-Extraction Kits

 

Spin-column viral DNA/RNA co-extraction kits purify both viral DNA and RNA in approximately 20 minutes from plasma, serum, nasopharyngeal swabs, urine, saliva, and CSF using a single-buffer lysis and Zymo-Spin silica-membrane column in a standard microcentrifuge.

MBP carries Zymo Research Quick-DNA/RNA Viral kits validated for 10+ virus families, available to registered vendors at Howard Hughes Medical Institute, Vanderbilt University, and MD Anderson Cancer Center. Request a quote for spin-column viral DNA/RNA co-extraction kits optimized for rapid purification of viral nucleic acids from clinical and research samples by contacting customerservice@mbpinc.net.

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What are Spin-Column Viral DNA/RNA Co-Extraction Kits?

 

Spin-column viral DNA/RNA co-extraction kits purify viral DNA and RNA simultaneously from plasma, serum, urine, nasopharyngeal swabs, saliva, CSF, and cell culture media using a single-buffer lysis that disrupts viral particles and conditions nucleic acids to bind a Zymo-Spin silica-membrane column in a standard microcentrifuge. Both DNA and RNA elute together in 30-100 ul of DNase/RNase-free water, ready for multiplex RT-qPCR targeting RNA viruses (SARS-CoV-2, influenza A/B, RSV, HIV) and DNA viruses (adenovirus, herpesvirus, HPV, parvovirus) from the same eluate in a single assay. Choose the spin-column viral DNA/RNA format when processing fewer than 50 samples per run, when only a microcentrifuge is available, or when the fastest possible turnaround from sample to detectable eluate is required for point-of-care adjacent testing.

 

What you will find:

 

  • Quick-DNA/RNA™ Viral Kit (D7020): Efficient spin-column technology designed for the fast co-purification of high-quality viral RNA and viral DNA from liquid specimens.

  • Virus RNA Kit (R6620-00): Specialized silica-membrane columns created for sensitive extraction of viral RNA, guaranteeing pure yields for subsequent detection processes.

  • MV Total RNA Isolation (R6313-01): Custom extraction columns designed for the retrieval of total RNA from difficult molecular biology samples, ensuring reliable recovery.

 

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

 

Single-Buffer vs. Multi-Buffer Lysis

Zymo Quick-DNA/RNA Viral Kit uses a single-step lysis buffer -- no protease incubation, no carrier RNA addition, no ethanol mixing before column loading. This reduces protocol complexity and per-batch error rate. Multi-buffer kits (QIAGEN QIAamp, Thermo PureLink) require preparation of lysis buffer + carrier RNA + ethanol before loading; they are comparable in yield but add setup time per batch.

Input Volume Flexibility

Standard spin-column viral kits accept 50-200 ul of cell-free sample. For low-titer samples requiring larger input volumes to increase sensitivity, check the kit for extended-input protocols; some kits allow 400-1,000 ul plasma with vacuum manifold loading. For samples in the DNA/RNA Shield, direct loading is validated without dilution.

DNA+RNA vs. RNA-Only Recovery

Confirm you need co-extraction before ordering. If your panel includes only RNA viral targets (influenza, RSV, SARS-CoV-2), an RNA-only viral spin-column kit produces equivalent sensitivity with a simpler protocol. Co-extraction is essential when your panel includes HPV, adenovirus, CMV, EBV, parvovirus, or any other DNA virus target - RNA-only kits will under-recover or miss these targets.

Elution Volume and Downstream Assay

Elute in 30-50 ul for RT-qPCR sensitivity; the higher nucleic acid concentration produces Ct improvement of 0.5-1.5 cycles compared to 100 ul elution. For multiplex NGS library preparation, elute in 100 ul and quantify by Qubit dsDNA BR and RNA HS assays separately before library input normalization.

Throughput Scaling

When daily volumes exceed 24 samples, the spin-column format creates centrifuge bottlenecks. At >50 samples per run, transition to the Quick-DNA/RNA Viral 96-well plate format (vacuum manifold) or Quick-DNA/RNA Viral MagBead format (automation) for higher throughput.

 

Specifications Context

 

Performance benchmarks for spin-column viral DNA/RNA co-extraction: >=70% recovery of RNA and DNA spike-in controls, Ct within 2 cycles of reference extraction for validated viral targets, and A260/A280 >= 1.7 in eluates. The Zymo Quick-DNA/RNA Viral Kit uses a single buffer system validated for enteroviruses, rhinoviruses, coronaviruses (SARS-CoV-2), HIV, HCV, influenza A, flaviviruses (dengue, Zika), measles, parainfluenza, and parvovirus; the kit is used in Zymo's SARS-CoV-2 extraction workflow and has been adopted in published multiplex respiratory panel methods. Spin-column viral co-extraction kits are the standard format in clinical research labs processing 10-50 patient samples per run for research-use multiplex RT-qPCR panels at institutions including Vanderbilt University and MD Anderson Cancer Center.

 

For kit recommendations, bulk pricing on Quick-DNA/RNA Viral spin-column kits, or guidance on pairing with multiplex RT-qPCR panels, contact the MBP team. MBP is a registered vendor for Howard Hughes Medical Institute, Vanderbilt University, and MD Anderson Cancer Center.

FAQ

Spin-column viral DNA/RNA co-extraction kits purify both viral DNA and viral RNA from cell-free biological samples — plasma, serum, urine, nasopharyngeal swabs, saliva, and cell culture media — using a single chaotropic lysis buffer that lyses viral particles and releases nucleic acids for binding to a Zymo-Spin silica-membrane column in a standard microcentrifuge. Both DNA and RNA are eluted together in 30–100 µl of DNase/RNase-free water, ready for multiplex RT-qPCR, pan-pathogen RT-PCR, and NGS library preparation.
The Zymo Quick-DNA/RNA Viral Kit (spin-column) completes lysis, column binding, two wash steps, and elution in approximately 20 minutes per batch of 1–50 samples using a standard microcentrifuge. The single-buffer lysis system eliminates protease pre-treatment and carrier RNA addition steps required by some competing kits, reducing total hands-on time and pipetting steps in routine diagnostic workflows.
The Zymo Quick-DNA/RNA Viral Kit (spin-column) accepts plasma, serum, urine, saliva, nasopharyngeal swab eluates, oropharyngeal swab eluates, cerebrospinal fluid, cell culture media, and any biological sample stored or stabilized in Zymo DNA/RNA Shield. Samples in standard viral transport media (VTM, UTM) are compatible without modification. Whole blood and tissue homogenates require dedicated formats with additional lysis steps beyond the standard viral spin-column protocol.
Yes. The Zymo Quick-DNA/RNA Viral 96 Kit is specifically validated for parvovirus, a ssDNA virus, demonstrating that the kit's silica-binding chemistry recovers single-stranded DNA alongside RNA viral genomes from the same extraction. This broad recovery makes the kit suitable for pan-pathogen panels including B19V parvovirus detection in plasma for aplastic crisis diagnostics alongside RNA virus targets.
Spin-column viral DNA/RNA kits elute into 30–100 µl of DNase/RNase-free water; 30–50 µl is recommended for sensitive RT-qPCR from low-titer clinical samples where concentrating nucleic acids improves detection of low-copy targets. For NGS applications, elute into 100 µl to maximize total nucleic acid mass from the same column and reduce the number of replicate extractions needed for sufficient library input.
Yes. Zymo Quick-DNA/RNA Viral Kits are used in Zymo Research's SARS-CoV-2 extraction workflow and have been validated for SARS-CoV-2 RNA detection from nasopharyngeal swabs by RT-qPCR. The Quick-DNA/RNA Viral MagBead format received Emergency Use Authorization for SARS-CoV-2 diagnostic use; the spin-column format is used in research and validated diagnostic settings using authorized RT-qPCR assays. Contact MBP for guidance on regulatory compliance for IVD applications.
The Zymo Quick-DNA/RNA Viral Kit uses a single proprietary lysis buffer that simultaneously lyses viral envelopes and protein capsids, denatures co-purified proteins and RNases, and conditions nucleic acids to bind the Zymo-Spin silica membrane in the first pipetting step. This contrasts with multi-step protocols (QIAGEN QIAamp) that require separate lysis buffer, ethanol addition, and carrier RNA preparation before loading onto the column, adding 5–10 minutes per batch and additional pipetting error opportunities.
Include an RNA spike-in (e.g., Caenorhabditis elegans cel-miR-39 at 1.6×10⁸ copies per extraction) added at the lysis step to monitor RNA extraction efficiency and detect inhibitor carryover, alongside an internal DNA spike-in control for DNA recovery monitoring. Acceptable performance is Ct within 2 cycles of the expected spike-in value. Run a negative extraction control (water or negative matrix) in every batch to detect contamination. For clinical diagnostic applications, use an extraction control included in the authorized RT-qPCR assay kit.
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