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Cells, Tissue & Blood DNA/RNA Co-Extraction Kits

 

Cells/tissue/blood DNA/RNA co-extraction kits simultaneously purify genomic DNA and total RNA from mammalian cell pellets, solid tissue biopsies, and whole blood in a single workflow that delivers separate fractions in under 15 minutes. Column-switching architecture physically separates gDNA from RNA before column binding—no sample splitting required.

MBP carries Zymo Research Quick-DNA/RNA Miniprep Plus, Microprep Plus, and MagBead kits for registered vendors, including Howard Hughes Medical Institute, Vanderbilt University, and MD Anderson Cancer Center. Request a quote for DNA/RNA co-extraction kits designed for mammalian cells, tissue biopsies, and blood samples requiring matched genomic and transcriptomic analysis by contacting customerservice@mbpinc.net.

Cells/Tissue/Blood

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Blood RNA Mini Kit
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USD53.48 - USD708.29
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USD38.20 - USD505.92
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Quick-DNA/RNA Miniprep Plus Kit
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USD155.61 - USD638.40
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USD111.15 - USD456.00
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Quick-DNA/RNA™ MagBead
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USD573.23 - USD1,839.39
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USD409.45 - USD1,313.85
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Quick-DNA/RNA™ Microprep Plus Kit
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USD174.23 - USD638.40
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USD124.45 - USD456.00
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Quick-DNA/RNA™ Miniprep
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USD26.60 - USD520.03
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USD19.00 - USD371.45
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What are Cells/Tissue/Blood DNA/RNA Co-Extraction Kits?

 

Cells/tissue/blood DNA/RNA co-extraction kits simultaneously purify genomic DNA and total RNA from the same mammalian cell pellet, solid tissue biopsy, or blood sample in a single lysis and purification workflow that delivers separate DNA and RNA fractions without splitting the input. The approach conserves sample and eliminates the spatial heterogeneity introduced when a tissue biopsy is cut into two portions for separate DNA and RNA extractions, a significant limitation for samples with variable cellularity (tumor biopsies, mixed-cell-type tissues). Choose a cells/tissue/blood co-extraction kit when paired genomic sequencing and transcriptome data are required from the same physical sample, when sample volume is limited, or when downstream analyses demand that DNA and RNA originate from the same exact cellular population.

 

What you will find:

 

  • Spin-column: Efficient silica-membrane kits including Quick-DNA/RNA™ Miniprep (D7001), Microprep Plus (D7005), and specialized Blood RNA Mini (R6411-00) tools for rapid, manual purification workflows.
  • Mag Beads: Automated, high-throughput separation systems utilizing the Quick-DNA/RNA™ MagBead Kit (R2130) for high-yield, magnetic-based nucleic acid co-extraction.

 

How to Choose a Cells/Tissue/Blood DNA/RNA Co-Extraction Kit

 

Input Format: Cells vs. Tissue vs. Blood

For cell culture pellets (up to 5x10^6 cells): the Zymo Quick-DNA/RNA Miniprep or Miniprep Plus Kit provides the broadest compatibility. For solid tissue biopsies (up to 30 mg): the Plus kit (with DNA/RNA Shield and Proteinase K) handles tissue disruption without additional grinding. For whole blood (up to 50 ul): the Miniprep Plus kit is validated; for larger blood volumes requiring higher RNA mass, consider a dedicated blood RNA system for the RNA fraction. For very small inputs (needle biopsy cores, 500-5,000 cells): use the Microprep Plus Kit with 6-25 ul elution volume.

Spin-Column vs. Magnetic Bead Format

Spin-column co-extraction kits (Quick-DNA/RNA Miniprep, QIAGEN AllPrep) handle 1-24 samples per run and require only a microcentrifuge. The Quick-DNA/RNA MagBead Kit processes 96 samples per run on compatible automation platforms including Tecan, Hamilton, and Beckman Biomek. For clinical sample processing programs, gene therapy tissue panels, or large AAV biodistribution studies (10+ tissues x multiple animals), the magnetic bead format provides the throughput that prevents bottlenecks.

DNase I Treatment for the RNA Fraction

Physical gDNA depletion via the IIICG/IICR column-switching architecture removes most genomic DNA from the RNA fraction. For RNA-seq applications where any gDNA mapping artefacts are unacceptable, add the optional on-column DNase I treatment step using the included DNase I enzyme in Plus kits. Validate gDNA removal with a no-reverse-transcriptase control in RT-qPCR before proceeding to RNA-seq library preparation.

Small RNA Retention

If downstream applications include miRNA quantification, miRNA-seq, or small RNA sequencing alongside RNA-seq, confirm the kit retains RNAs >=17 nt. Zymo Quick-DNA/RNA kits retain the full small RNA spectrum on the IC column. QIAGEN AllPrep DNA/RNA kits under standard protocol retain RNA >=200 nt; a modified protocol in the AllPrep Micro Kit handbook enables small RNA retention from cell inputs.

FFPE Tissue

For archived FFPE tissue where both DNA mutation and RNA expression data are needed from the same section (paired cancer sequencing and transcriptomics), use the Zymo Quick-DNA/RNA FFPE Miniprep Kit, which includes deparaffinization solution, Proteinase K, and heat-mediated crosslink reversal for recovery of crosslinked DNA and fragmented RNA from paraffin-embedded material.

 

Specifications Context

 

Quality benchmarks for cells/tissue/blood co-extractions: DNA A260/A280 >= 1.8, fragment size >= 20 kb for whole-exome sequencing (>= 5 kb minimum for most NGS workflows); RNA A260/A280 >= 1.8, RIN >= 7 from fresh tissue (RIN 3-6 from FFPE). The Zymo Quick-DNA/RNA Miniprep Plus Kit delivers DNA and total RNA (including small RNAs >=17 nt) from any biological sample in less than 15 minutes, with both analytes ready for next-generation sequencing, RT-qPCR, and microarray without further cleanup. DNA/RNA co-extraction from the same tissue input is standard practice in cancer multi-omics research and gene therapy biodistribution studies - a 2024 PMC-published study validated automated co-extraction across 10 tissue types for simultaneous AAV vector copy number (DNA, qPCR) and transgene expression analysis (RNA, RT-qPCR), achieving a 100% sample pass rate for both analytes.

 

For kit selection guidance and pricing on the Zymo Quick-DNA/RNA product line for cells, tissue, and blood applications, contact the MBP team.

FAQ

Cells/tissue/blood DNA/RNA co-extraction kits simultaneously isolate high-quality genomic DNA and total RNA — including small RNAs ≥17 nt — from mammalian cell cultures, solid tissue biopsies, and whole blood in a single lysis and purification workflow that delivers both analytes in separate fractions. The approach conserves precious sample by eliminating the need to split a tissue biopsy between separate DNA and RNA extractions, ensuring both analytes originate from the same cellular population.
The Zymo Research Quick-DNA/RNA Miniprep Plus Kit and Quick-DNA/RNA MagBead Kit are validated for fresh and frozen mammalian cell pellets (up to 5×10⁶ cells), solid tissue biopsies (up to 30 mg), whole blood (up to 50 µl), buffy coat, buccal cells, plasma, and serum. The QIAGEN AllPrep DNA/RNA Mini Kit is validated for cells and tissue (up to 30 mg). For FFPE tissue, use the Zymo Quick-DNA/RNA FFPE Miniprep Kit with its deparaffinization and crosslink-reversal protocol.
The Zymo Quick-DNA/RNA Miniprep Plus Kit uses a sequential column-loading design: the lysate is first loaded onto a Zymo-Spin IIICG column that binds gDNA, and the flow-through containing RNA is then transferred to a Zymo-Spin IC column for RNA binding, washing, and elution. Each analyte is separately washed and eluted in its own collection tube. The QIAGEN AllPrep DNA/RNA Kit uses an AllPrep DNA spin column (DNA binds first), then the flow-through loads an RNeasy column for RNA purification.
From 5×10⁶ mammalian cells, the Zymo Quick-DNA/RNA Miniprep Plus Kit yields 5–15 µg gDNA and 5–20 µg total RNA per extraction, with both analytes eluting in 25–100 µl. From 30 mg of soft tissue (liver, spleen), yields are 5–30 µg DNA and 5–50 µg RNA. Whole blood (50 µl) yields 0.5–2 µg DNA and 0.5–3 µg RNA. Tissue-specific differences in nucleic acid content, RNA integrity, and inhibitor presence affect yields; fibrous tissues (muscle, heart) consistently yield less RNA than metabolically active tissues.
The column-switching architecture in Zymo Quick-DNA/RNA kits physically separates the vast majority of gDNA onto the IIICG column before RNA binds the IC column, reducing gDNA contamination in the RNA fraction to below detectable levels for most applications. For RNA-seq and RT-qPCR applications requiring stringent gDNA removal, an optional on-column DNase I treatment step can be added to the IC column after RNA binding; the Quick-DNA/RNA Plus kits include DNase I for this purpose.
The Zymo Quick-DNA/RNA Miniprep Plus Kit processes up to 50 µl of whole blood per extraction by lysing red blood cells and recovering DNA from leukocytes alongside total RNA from the same input. For larger blood volumes (1–5 ml PAXgene or EDTA blood) where more RNA mass is required for expression profiling, use a dedicated blood RNA kit (PAXgene Blood RNA Kit) for the RNA fraction and a separate blood DNA kit for gDNA.
Yes. The Zymo Quick-DNA/RNA kits use a Zymo-Spin IC column with binding chemistry that retains small RNAs ≥17 nt alongside mRNA and rRNA from the same cell or tissue lysate. Co-extraction of miRNAs and siRNAs from the same sample as gDNA enables integrated analyses correlating small RNA-mediated gene regulation with genomic sequence, which is relevant for cancer biology, gene therapy studies, and miRNA biomarker research.
The Zymo Quick-DNA/RNA Microprep Plus Kit is optimized for very small inputs: as few as 1,000 cells or 0.5 mg of tissue per extraction, eluting DNA and RNA in 6–25 µl per fraction for concentrated recovery from limited material. This format is suitable for needle biopsy cores, laser-capture microdissected cells, sorted cell populations, and organoid cultures where the total available input is below the minimum required for standard miniprep kits. The QIAGEN AllPrep DNA/RNA Micro Kit similarly covers inputs from 10 mammalian cells upward.
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