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Spin-Column DNA/RNA Co-Extraction Kits with Dual-Column Separation

 

Spin-column DNA/RNA co-extraction kits simultaneously isolate genomic DNA and total RNA in separate fractions from the same mammalian cell pellets (up to 5×10⁶), tissue biopsies (up to 30 mg), and whole blood (up to 50 µl) in under 15 minutes using a two-column Zymo-Spin architecture—IIICG for gDNA capture, IIC for RNA purification—with DNase I included for on-column RNA fraction cleanup.

MBP carries the Zymo Research Quick-DNA/RNA Miniprep Plus and Microprep Plus kits for registered vendors at Howard Hughes Medical Institute, Vanderbilt University, and MD Anderson Cancer Center. Request a quote for spin-column DNA/RNA co-extraction kits featuring separate genomic DNA and RNA recovery for downstream PCR, qPCR, sequencing, and multi-omics applications by contacting customerservice@mbpinc.net.

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Blood RNA Mini Kit
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Quick-DNA/RNA Miniprep Plus Kit
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Quick-DNA/RNA™ Microprep Plus Kit
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Quick-DNA/RNA™ Miniprep
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What are Spin-Column DNA/RNA Co-Extraction Kits for Cells, Tissue, and Blood?

 

Spin-column DNA/RNA co-extraction kits for cells, tissue, and blood simultaneously purify genomic DNA and total RNA in separate fractions from the same mammalian sample using a sequential two-column silica-membrane workflow in a standard microcentrifuge. The Zymo Quick-DNA/RNA Miniprep Plus Kit loads the sample lysate onto a Zymo-Spin IIICG column that physically captures gDNA while RNA passes through to a Zymo-Spin IIC column for binding, washing, and elution - completing both DNA and RNA purification in under 15 minutes for cell pellets and 45-75 minutes (including Proteinase K digestion) for solid tissue biopsies. Choose the spin-column format for DNA/RNA co-extraction from cells, tissue, and blood when processing 1-24 samples per run, when automation infrastructure is not available, or when the fastest possible DNA + RNA turnaround from a limited biopsy sample is required.

 

What you will find:

 

  • Quick-DNA/RNA™ Miniprep Kit for rapid co-extraction of total DNA and RNA from blood and tissues utilizing advanced spin-column technology

  • Quick-DNA/RNA™ Microprep Plus Kit to recover high-purity nucleic acids from extremely small or rare samples using a specialized micro-elution column

  • Quick-DNA/RNA Miniprep Plus Kit to ensure high-yield genomic DNA and total RNA yields using an ultra-clean spin-column workflow

  • Blood RNA Mini Kit for the specific extraction of intact viral and total host RNA from whole blood samples using robust silica-membrane columns

 

How to Choose a Spin-Column DNA/RNA Co-Extraction Kit for Cells, Tissue, and Blood

 

Miniprep Plus vs. Microprep Plus Format

The Miniprep Plus kit handles standard inputs (up to 5x10^6 cells or 30 mg tissue) and elutes in 25-100 ul per fraction, appropriate for most downstream applications. The Microprep Plus kit is designed for very low inputs -- 500 cells to 5,000 cells or 0.5-5 mg tissue -- with minimum elution volumes of 6-10 ul per fraction for maximum concentration from limited material. Use Microprep Plus for needle biopsy cores, laser-capture microdissected cells, single-well organoid lysates, and sorted immune cell populations.

DNA/RNA Shield for Sample Lysis and Stabilization

DNA/RNA Shield in the Miniprep Plus and Microprep Plus kits performs dual duty: it lyses cells on contact while simultaneously stabilizing DNA and RNA at room temperature, enabling sample collection and processing to be decoupled by hours or days without cold-chain handling. For tissue biopsies collected in the operating room that cannot be processed immediately, submerging in DNA/RNA Shield preserves RNA integrity for up to 30 days at room temperature -- the practical alternative to snap-freezing in liquid nitrogen.

Tissue Digestion Strategy

Soft, high-cellularity tissues (liver, spleen, kidney cortex) lyse completely in DNA/RNA Shield + Proteinase K at 55 degrees C within 30 minutes. Fibrous tissues (skeletal muscle, heart, skin, lung) require 1-2 hours of Proteinase K digestion or mechanical homogenization (bead-beating, tissue grinder) before column loading. For very fibrous tissue that resists Proteinase K digestion, add bead-beating in a lysis tube (0.5 mm beads) with DNA/RNA Lysis Buffer before proceeding to column loading.

On-Column DNase I for the RNA Fraction

Always include on-column DNase I treatment for RNA-seq and for RT-qPCR assays without intron-spanning primers. Skip DNase I only for RT-qPCR with exon-spanning primer pairs that distinguish cDNA from gDNA amplicons. The IIICG column physically depletes the majority of gDNA but does not eliminate 100%; residual gDNA in the RNA fraction produces false-positive amplification in RT-qPCR assays without an intron-spanning design.

Elution Strategy for Downstream Applications

For RNA-seq: elute RNA in 50-100 ul, quantify by Qubit RNA HS Assay, and verify RIN >= 7 on a Bioanalyzer before library preparation. For RT-qPCR: elute in 25-50 ul for higher RNA concentration. For gDNA applications requiring >= 5 kb fragments (WGS, WES, long-read sequencing): elute DNA in 50-100 ul and quantify by Qubit dsDNA BR Assay; avoid vortexing gDNA eluates to preserve high-molecular-weight fragment integrity.

 

Specifications Context

 

The Zymo Quick-DNA/RNA Miniprep Plus Kit produces gDNA (A260/A280 >= 1.8, high molecular weight >= 20 kb) and total RNA, including small RNAs >=17 nt (A260/A280 >= 1.8, RIN >= 7 from fresh tissue) in under 15 minutes from cell pellets, with both analytes ready for next-generation sequencing without further cleanup. The Quick-DNA/RNA Miniprep Plus Kit is among the most widely used spin-column co-extraction kits in academic molecular biology, gene therapy, pharmacology, and cancer multi-omics research; its use is cited in published studies at institutions including Howard Hughes Medical Institute, Vanderbilt University, and MD Anderson Cancer Center for paired genomic and transcriptomic analyses. For needle biopsy or LCM inputs where the Miniprep Plus minimum input cannot be met, the Microprep Plus format recovers both analytes from the single-cell level without carrier RNA or pre-amplification requirements.

 

For guidance on selecting the right spin-column co-extraction format for your input type or for pricing, contact the expert team at MBP Inc.

FAQ

Spin-column DNA/RNA co-extraction kits for cells, tissue, and blood simultaneously isolate genomic DNA and total RNA in separate fractions from the same mammalian sample using a sequential two-column silica-membrane workflow in a standard microcentrifuge. The Zymo Quick-DNA/RNA Miniprep Plus Kit uses a Zymo-Spin IIICG column to capture gDNA from the lysate, then transfers the RNA-containing flow-through to a Zymo-Spin IIC column for RNA purification, completing co-extraction from up to 5×10⁶ cells or 30 mg of tissue in under 15 minutes.
The Zymo Quick-DNA/RNA Miniprep Plus Kit co-extracts both DNA and RNA from up to 5×10⁶ mammalian cells in less than 15 minutes, delivering both fractions ready for downstream use. The protocol involves adding DNA/RNA Shield and Proteinase K to the sample, loading the lysate sequentially onto two spin columns with wash and elution steps for each analyte. For tissue samples requiring Proteinase K digestion, add a 30–60 minute pre-incubation step at 55°C before column loading.
Yes. The Zymo Quick-DNA/RNA Miniprep Plus Kit includes DNase I for optional on-column treatment of the Zymo-Spin IIC RNA column, which removes residual gDNA from the RNA fraction after physical depletion on the IIICG column. For RNA-seq applications, include on-column DNase I treatment; for RT-qPCR applications using intron-spanning primers, the physical IIICG depletion alone is often sufficient, but adding DNase I is recommended for highest-quality results.
For solid tissue biopsies (up to 30 mg), the Zymo Quick-DNA/RNA Miniprep Plus protocol uses DNA/RNA Shield to stabilize and begin lysis, followed by Proteinase K digestion at 55°C for 30 minutes, then mechanical disruption by bead beating or needle homogenization, before loading the cleared lysate onto the IIICG column for sequential DNA and RNA purification. Fibrous tissues (muscle, heart, connective tissue) require longer Proteinase K digestion (up to 2 hours) or initial mechanical disruption to achieve complete lysis.
For a 5 mg needle biopsy core, splitting into separate DNA and RNA extractions leaves each aliquot below the minimum input of most standard kits (typically 10–30 mg), producing insufficient yield from both analytes. Spin-column co-extraction processes the entire 5 mg input on a single IIICG/IIC column pair, delivering usable DNA and RNA quantities from inputs that would fail single-analyte extraction if split. The Zymo Quick-DNA/RNA Microprep Plus Kit extends this advantage to inputs as small as 500 cells or 0.5 mg of tissue.
From 5 mg of mouse liver (a high-RNA tissue), the Zymo Quick-DNA/RNA Miniprep Plus Kit typically yields 1–5 µg gDNA and 2–10 µg total RNA per extraction, each in 25–100 µl elution volume. From 5×10⁶ HeLa cells, expected yields are 5–15 µg DNA and 5–20 µg RNA. For fibrous tissues (skeletal muscle, heart), yields are 2–5-fold lower per mg input due to lower cellularity and higher collagen content. Qubit RNA HS Assay provides accurate RNA concentration measurement below 500 ng/µl where spectrophotometry becomes less reliable.
The Zymo Quick-DNA/RNA Miniprep Plus Kit processes up to 50 µl of whole blood per extraction, lysing red blood cells and co-extracting DNA from leukocytes and total RNA from nucleated blood cells. For higher blood volumes or applications requiring higher RNA yield, use PAXgene Blood RNA System tubes for blood collection and dedicated RNA extraction, paired with a separate blood DNA kit for gDNA isolation.
If a no-reverse-transcriptase RT-qPCR control produces amplification signal in the co-extracted RNA fraction, add on-column DNase I treatment: after loading the lysate flow-through onto the Zymo-Spin IIC column and performing the first wash, apply 80 µl of reconstituted DNase I Reaction Mix directly to the column membrane and incubate at room temperature for 15 minutes before continuing with the wash and elution steps. Repeat the RT-qPCR minus-RT control to confirm gDNA is below detection.
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