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FFPE DNA/RNA Co-Extraction Kits for Archival Tissue

 

FFPE DNA/RNA co-extraction kits simultaneously isolate genomic DNA and total RNA from the same formalin-fixed paraffin-embedded tissue section using xylene-free deparaffinization, Proteinase K digestion, heat crosslink reversal, and Zymo-Spin column purification—delivering separate DNA and RNA fractions from a single undivided FFPE section. Co-extraction conserves limited archival material and ensures both analytes reflect the same tissue population for paired cancer multi-omics.

MBP carries Zymo Research Quick-DNA/RNA FFPE Miniprep Kits for registered vendors at Howard Hughes Medical Institute, Vanderbilt University, and MD Anderson Cancer Center. Request a quote for FFPE DNA/RNA co-extraction kits by contacting customerservice@mbpinc.net.

FFPE

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Quick-DNA/RNA™ FFPE MiniPrep (50 Preps.)
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USD559.93
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USD399.95
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What are FFPE DNA/RNA Co-Extraction Kits?

 

FFPE DNA/RNA co-extraction kits simultaneously isolate genomic DNA and total RNA -- including small RNAs >=17 nt from the same formalin-fixed paraffin-embedded tissue section using xylene-free deparaffinization, Proteinase K digestion, heat-mediated formaldehyde crosslink reversal, and Zymo-Spin column purification. Co-extraction from a single undivided FFPE section conserves precious archival material and ensures both DNA (for somatic mutation calling, CNV analysis, methylation profiling) and RNA (for expression profiling, fusion detection, nCounter panels) originate from identical tissue, eliminating the spatial heterogeneity introduced when different tissue sections or block portions are used for each analyte. Use an FFPE DNA/RNA co-extraction kit whenever archival tissue is limited, as in needle biopsy cores, small surgical biopsies, or rare tumour specimens, or when integrated multi-omic analysis (paired WES + RNA-seq, or mutation + expression correlation) is required from the same pathological specimen.

 

What you will find:

 

  • Quick-DNA/RNA™ FFPE MiniPreps: Efficient systems designed to extract high-quality total nucleic acids with reduced sequence bias, tailored for subsequent qPCR and NGS library preparation.

  • Decross-linking Agents: Nuclease-free solutions formulated to effectively liberate nucleic acids from protein complexes, ensuring transfection-grade purity for delicate bioinformatics workflows.

 

How to Choose an FFPE DNA/RNA Co-Extraction Kit

 

Xylene-Free vs. Xylene-Based Deparaffinization

Zymo Research Quick-DNA/RNA FFPE Miniprep Kit uses a proprietary Deparaffinization Solution that removes paraffin without xylene, making it safer for labs without fume hoods and eliminating toxic waste disposal requirements.

Tissue Section vs. Tissue Block Curling

For formalin-fixed paraffin-embedded sections on slides, cut and scrape sections directly into the Deparaffinization Solution tube - 2-4 sections of 5-10 um thickness is the standard starting point. For tissue blocks, cut 10-20 um sections with a microtome into a 1.5 ml tube. Avoid over-cutting; excessive paraffin volume from thick sections delays deparaffinization and reduces proteinase K efficiency, leading to lower DNA and RNA yields.

DNA and RNA Fraction Separation

The Zymo Quick-DNA/RNA FFPE Miniprep Kit delivers non-crosslinked DNA and DNA-free total RNA in separate fractions, making it suitable for downstream molecular analyses from the same FFPE sample.

Amplicon Size for Downstream Assays

RNA isolated from FFPE tissue is typically fragmented because of formalin fixation. For RT-qPCR, primer pairs producing amplicons of approximately 70–150 bp generally provide the most reliable amplification. The purified RNA from the Quick-DNA/RNA™ FFPE MiniPrep is suitable for downstream applications including RT-PCR, next-generation sequencing (NGS), microarray analysis, and hybridization, provided library preparation and assay workflows are compatible with fragmented FFPE-derived nucleic acids.

Block Age Assessment

Request pathology records for fixation time and block age before extraction. For blocks >10 years old, perform a diagnostic RT-qPCR on a short amplicon (60-80 bp) reference gene in the RNA fraction before committing to full RNA-seq library preparation. RNA from blocks with Ct >35 for abundant reference genes (ACTB, GAPDH) at short amplicons typically fails RNA-seq quality thresholds.

 

Specifications Context

 

The Zymo Quick-DNA/RNA™ FFPE Miniprep Kit delivers non-crosslinked DNA and DNA-free total RNA (including small RNAs ≥17 nt) from FFPE tissue using a xylene-free deparaffinization workflow. The purified nucleic acids are suitable for downstream applications including PCR, RT-PCR, next-generation sequencing (NGS), hybridization, and other molecular analyses compatible with FFPE-derived samples. Because formalin fixation fragments nucleic acids, downstream assays are generally designed with short amplicons (approximately 60–150 bp for RNA and 100–300 bp for DNA) to improve amplification efficiency. Co-isolation of DNA and RNA from the same FFPE specimen supports integrated genomic and transcriptomic analyses while preserving limited archival tissue.

 

For FFPE kit selection, bulk pricing on Zymo Quick-DNA/RNA FFPE Miniprep kits, or protocol guidance for aged or low-cellularity archival blocks, contact the MBP team

FAQ

FFPE DNA/RNA co-extraction kits simultaneously isolate genomic DNA and total RNA from the same formalin-fixed paraffin-embedded tissue section or block — the dominant archival format for surgical pathology specimens — using a single workflow that includes paraffin removal, Proteinase K digestion to dissolve crosslinked proteins, heat-mediated reversal of formaldehyde-induced nucleic acid crosslinks, and Zymo-Spin column purification delivering both analytes from one undivided tissue input.
Standard practice separates a tissue section or block into two portions — one for DNA extraction and one for RNA extraction — introducing spatial heterogeneity when the tissue has variable cellular composition (tumor microenvironment, stromal admixture, necrotic areas). Co-extraction from the same undivided section ensures both DNA (for somatic mutation calling) and RNA (for gene expression profiling or fusion detection) originate from the same cellular population, improving concordance in multi-omic FFPE cancer studies and conserving precious archival material.
MBP carries the Zymo Research Quick-DNA/RNA FFPE Miniprep Kit, which uses a proprietary xylene-free Deparaffinization Solution for paraffin removal, followed by Proteinase K digestion and heat-mediated crosslink reversal, then Zymo-Spin column purification to deliver high-quality non-crosslinked DNA and DNA-free total RNA (including small RNAs ≥17 nt) from the same FFPE tissue input, ready for PCR, NGS, RT-PCR, and hybridization-based applications.
The Zymo Quick-DNA/RNA FFPE Miniprep Kit uses a proprietary Deparaffinization Solution that removes paraffin without xylene, eliminating fume-hood requirements and toxic waste handling for the deparaffinization step. The QIAGEN AllPrep DNA/RNA FFPE Kit uses a Deparaffinization Solution compatible with standard laboratory conditions; an alternative xylene-based deparaffinization protocol is available in the QIAGEN kit handbook for labs already equipped for xylene use.
The Zymo Quick-DNA/RNA FFPE Miniprep Kit processes up to 25 mg of FFPE tissue or up to four tissue sections ≤20 µm thick with a total surface area of approximately 20 mm² per extraction. Start with 1–2 sections on first use to establish optimal protocol conditions before committing larger material from limited archival blocks. Highly cellular tumour tissue yields more nucleic acids per section than fibrous stromal or necrotic areas.
FFPE DNA is typically fragmented to 100–500 bp by formaldehyde crosslinking and fixation; whole-exome sequencing of FFPE DNA requires library preparation kits validated for fragmented input (e.g., KAPA HyperPlus, Illumina DNA Prep). FFPE RNA has RIN values of 1–4 for blocks >5 years old and 3–6 for recent blocks (<3 years); RNA-seq from FFPE requires fragmented-RNA-compatible library preparation (Illumina TruSeq RNA Exome, Takara SMART-Seq FFPE). Both analytes from the Zymo FFPE kit are confirmed ready for PCR, NGS, and hybridization-based assays.
Yes. RNA from FFPE co-extraction is used for oncogenic gene fusion detection by RT-PCR and RNA-seq — a critical diagnostic application in lung cancer (EML4-ALK, ROS1), colorectal cancer (NTRK1/2/3), and haematological malignancies (BCR-ABL1, PML-RARA). For RNA-seq-based fusion detection from FFPE, use a library preparation kit validated for fragmented RNA input (Lexogen TeloPrime, Takara SMART-Seq FFPE) that employs template-switching or ligation-based approaches to capture truncated transcripts typical of FFPE RNA.
RNA quality from FFPE decreases with block age and time in fixative: blocks fixed for <24 hours and stored <3 years typically yield RNA assessable at 100–200 bp amplicons; blocks >10 years old may only support amplicons of 60–100 bp. DNA quality is more resilient — FFPE DNA is extractable from blocks decades old — but fragment size decreases with age. For the RNA fraction, NCI Biospecimen Evidence-Based Practices guidelines (updated 2025) recommend prioritizing short amplicon RT-PCR assay design (60–150 bp) for FFPE RNA from all block ages.
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