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Cell-Free DNA/RNA Co-Extraction Kits for Liquid Biopsy

 

Cell-free DNA/RNA co-extraction kits simultaneously isolate circulating cfDNA (ctDNA, apoptotic DNA fragments 130–250 bp) and cfRNA (microRNAs, lncRNAs, exosomal RNA) from the same plasma, serum, or urine sample using phenol-free spin-column chemistry—recovering up to 515x more microRNA than conventional methods. 

MBP carries Zymo Research Quick-cfDNA/cfRNA Serum & Plasma Kits for multi-omic liquid biopsy workflows. Request a quote for cell-free DNA/RNA co-extraction kits supporting liquid biopsy, ctDNA analysis, circulating microRNA profiling, and multi-omic biomarker discovery workflows by contacting customerservice@mbpinc.net.

Cell-free DNA/RNA

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Quick-cfDNA/cfRNA™ Serum & Plasma Kit (50 Preps.)
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USD1,359.26
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USD970.90
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What are Cell-Free DNA/RNA Co-Extraction Kits?

 

Cell-free DNA/RNA co-extraction kits simultaneously isolate circulating cell-free DNA (cfDNA -- ctDNA fragments of 130-250 bp, apoptotic DNA) and cell-free RNA (cfRNA -- microRNAs, lncRNAs, exosomal RNA, circulating mRNA fragments) from the same plasma, serum, or urine sample without phenol-chloroform or protein precipitation, delivering both analytes for parallel liquid biopsy genomic and transcriptomic analysis from a single 1-4 ml blood draw. Unlike dedicated cfDNA kits that miss circulating RNA species, or cfRNA kits that under-recover short cfDNA fragments, co-extraction kits are formulated to bind both nucleic acid classes - including protein-bound RNA, exosomal RNA, and miRNA - from cell-free matrices where total nucleic acid concentration is 1-100 ng/ml. Use a cfDNA/cfRNA co-extraction kit when your liquid biopsy workflow requires both somatic mutation analysis (ctDNA sequencing) and RNA expression profiling (circulating miRNA or cfRNA-seq) from the same blood draw, or when sample volume is limited and splitting between separate DNA and RNA kits would leave insufficient input for either.

 

What you will find:

 

  • Quick-cfDNA/cfRNA™ Serum & Plasma Kit: An efficient spin-column setup tailored for sample volumes up to 3 ml, providing reduced sequence bias and recovering as much as 515 times more microRNA.

  • High-Purity Elution Technology: Nuclease-free methods enabling the separate or co-elution of nucleic acids, ensuring transfection-grade purity for delicate bioinformatics and RT-qPCR uses.

 

How to Choose a cfDNA/cfRNA Co-Extraction Kit

 

Input Volume and Assay Sensitivity

cfDNA concentration in cancer patient plasma ranges from 1-1,000 ng/ml depending on tumor stage and type; circulating miRNA concentration is typically 1-100 pg/ml. For low-MAF ctDNA detection (<0.1%), 2-4 ml plasma input is required to obtain sufficient copies for ddPCR or ultra-deep sequencing. For cfRNA profiling only, 200 μL-1 mL is sufficient for miRNA RT-qPCR panels. The Zymo Quick-cfDNA/cfRNA Kit scales linearly up to 3 ml input.

Co-Elution vs. Separate Fractions

The Zymo Quick-cfDNA/cfRNA Serum & Plasma Kit offers the option to co-elute DNA and RNA into a single fraction or to collect separate fractions. Co-elution maximizes nucleic acid recovery in the smallest volume -- optimal for low-abundance targets; separate fractions are needed when DNA-specific (bisulfite sequencing, whole-exome) and RNA-specific (rRNA depletion, miRNA-seq library) downstream protocols cannot use the same input.

miRNA Recovery

Circulating miRNAs (18-22 nt) are small, low-abundance, and easily lost during standard DNA extraction. Confirm the co-extraction kit explicitly recovers small RNAs <200 nt from plasma. The Zymo Quick-cfDNA/cfRNA Kit recovers up to 515x more microRNA than conventional phase-separation methods -- a validated difference confirmed in the Zymo product datasheet.

Phenol-Free Chemistry

For high-throughput liquid biopsy programs, phenol-free kits eliminate fume-hood requirements and toxic waste handling. The QIAGEN ccfDNA/RNA Kit and Zymo Quick-cfDNA/cfRNA Kit are both phenol-free; automated protocols using these kits can process large cohort batches without hazardous chemical handling steps.

Pre-Analytical Standardization

cfDNA/cfRNA concentrations vary with blood collection tube type, time-to-processing, and centrifugation protocol. Standardize on EDTA tubes + two-spin plasma preparation (300xg then 16,000xg) and process within 6 hours of collection or store at -80 degrees C. For samples requiring extended transport, Streck Cell-Free DNA BCT or cfRNA preservation tubes stabilize both analytes at room temperature for up to 7 days before extraction.

 

Specifications Context

 

The Zymo Quick-cfDNA/cfRNA Serum & Plasma Kit enables simple spin-column isolation of all circulating cell-free DNA and RNA from serum, plasma, and biological fluids, recovering protein-bound, exosomal, miRNA, and other small RNA in addition to cfDNA. Cell-free nucleic acids scale linearly with input volume up to 3 ml. A 2022 digital PCR comparative study (PMC9805675) evaluated multiple cfDNA/cfRNA co-purification kits across plasma input volumes of 0.06-4 ml, finding that combined cfDNA/cfRNA quantification produces higher total nucleic acid concentrations than parallel separate quantification. cfDNA/cfRNA multi-omic liquid biopsy is an active area of clinical translational research for non-invasive cancer diagnosis and treatment monitoring, with studies underway at MD Anderson Cancer Center and Vanderbilt University using co-extraction formats to maximize information per blood draw.

 

Close the gap between liquid biopsy and groundbreaking discovery—reach out to MBP Inc. now to obtain a quote for your next-generation sequencing requirements.

FAQ

Cell-free DNA/RNA (cfDNA/cfRNA) co-extraction kits simultaneously purify cell-free DNA — circulating tumor DNA (ctDNA), apoptotic DNA fragments of 130–250 bp — and cell-free RNA — circulating microRNAs, long non-coding RNAs, exosomal RNA, and mRNA fragments — from the same plasma, serum, or urine sample in a single phenol-free workflow that delivers both analytes for parallel genomic and transcriptomic liquid biopsy analysis from one blood draw.
Co-extraction from the same undivided plasma volume delivers both cfDNA and cfRNA from an identical sample fraction, enabling combined somatic mutation analysis (ctDNA sequencing) and non-coding RNA expression profiling (circulating miRNA panels) from a single 1–4 ml blood draw. A 2022 peer-reviewed digital PCR study (PMC9805675) demonstrated that combined cfDNA/cfRNA quantification from the same co-extracted eluate systematically produces higher total nucleic acid concentrations than parallel separate quantifications, improving sensitivity for low-allele-frequency tumor markers.
MBP carries the Zymo Research Quick-cfDNA/cfRNA Serum & Plasma Kit, which provides simple spin-column isolation of all circulating cell-free DNA and RNA — including protein-bound, exosomal, microRNA, and other small RNA — from serum, plasma, and other biological fluids, without phenol-chloroform or protein precipitation. The kit accepts inputs up to 3 ml of plasma or serum and recovers up to 515 times more microRNA than conventional methods; nucleic acids are eluted with the option to co-elute or receive separate fractions.
The Zymo Quick-cfDNA/cfRNA Serum & Plasma Kit processes up to 3 ml of plasma or serum per extraction with linear scaling of cell-free nucleic acid yield relative to input volume. For standard liquid biopsy ctDNA applications where mutant allele frequency (MAF) is low (<0.1%), 2–4 ml of plasma provides maximum sensitivity. For circulating miRNA profiling where input is limited to 200–500 µl from clinical draws, confirm yield meets minimum input requirements for your downstream RT-qPCR or small RNA-seq assay.
Yes. The Zymo Quick-cfDNA/cfRNA Serum & Plasma Kit recovers all circulating cell-free nucleic acid species including protein-bound RNA, exosomal RNA, microRNA (miR-21, miR-155, miR-210, and other cancer-associated species), and other small RNA in addition to fragmented cfDNA. The kit recovers up to 515 times more microRNA than conventional phase separation methods, as reported in Zymo Research's product documentation, making it significantly more sensitive for circulating miRNA biomarker studies than total RNA extraction kits applied to plasma.
Co-extracted cfDNA and cfRNA from plasma support: ctDNA sequencing for somatic mutation detection (ddPCR, NGS panels, whole-exome sequencing from plasma); circulating miRNA expression profiling by RT-qPCR or small RNA-seq; combined ctDNA + cfRNA multi-omic liquid biopsy assays for cancer diagnosis and treatment monitoring; circulating tumor RNA detection (fusion transcripts, aberrant splicing); and non-invasive prenatal testing (cell-free fetal DNA). Digital PCR is increasingly preferred for ctDNA quantification due to its higher sensitivity at low mutant allele frequencies (<0.1%).
Plasma is preferred over serum for cfDNA/cfRNA co-extraction. Serum preparation involves blood clotting, which lyses platelets and leukocytes, releasing abundant cellular DNA and RNA that dilutes and overwhelms cell-free nucleic acid fractions. EDTA plasma, collected by two-spin differential centrifugation (300×g then 16,000×g), produces the cleanest cell-free fraction with lowest cellular contamination. For samples at high risk of ctDNA degradation, Streck Cell-Free DNA BCT or cfRNA tubes preserve circulating nucleic acid integrity during extended transport before processing.
Spike a fixed amount of an exogenous non-human control RNA (Caenorhabditis elegans cel-miR-39, 1.6×10⁸ copies per extraction) and a DNA spike-in (synthetic non-human dsDNA fragment, 10⁴ copies per extraction) into every plasma sample at the lysis step. Quantify both spike-ins by RT-qPCR in the eluate; Ct within 2 cycles of the expected value confirms successful co-extraction. Inter-sample Ct variability in the spike-ins monitors both extraction efficiency and inhibitor carryover across batches.
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