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.
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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.
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.
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.
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.