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Spin-Column Bacterial and Fungal RNA Kits with BashingBead Lysis

 

Spin-column bacterial and fungal RNA extraction kits purify total RNA from Gram-positive bacteria, Gram-negative bacteria, yeast, and filamentous fungi in under 15 minutes using ultra-high-density BashingBead mechanical lysis and Zymo-Spin silica-membrane columns in a standard microcentrifuge. 

MBP carries Zymo Research Quick-RNA Fungal/Bacterial Miniprep and Microprep kits, validated for Aspergillus fumigatus, Candida albicans, S. cerevisiae, E. coli, and Staphylococcus aureus. Request a quote today by contacting customerservice@mbpinc.net.

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Pinpoint™ Slide RNA Isolation System I
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USD17.29 - USD460.18
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USD12.35 - USD328.70
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Quick-RNA™ Fungal/Bacterial MicroPrep Kit (50 Preps.)
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USD408.31
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USD291.65
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YeaStar™ RNA Kit (40 Preps.)
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USD236.74
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USD169.10
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ZR Fungal/Bacterial RNA MiniPrep (50 Preps.)
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What are Spin-Column Bacterial and Fungal RNA Extraction Kits?

 

Spin-column bacterial and fungal RNA extraction kits isolate total RNA from Gram-positive bacteria, Gram-negative bacteria, yeasts, filamentous fungi, algae, and protozoa using ultra-high-density BashingBead mechanical cell wall disruption in a chaotropic lysis buffer, followed by RNA binding to a Zymo-Spin silica-membrane column, on-column washing, and elution in 6-100 ul of RNase-free water - all using a standard microcentrifuge. The complete protocol takes under 15 minutes for a batch of 1-12 samples, requiring only a vortex with a microcentrifuge tube adapter, a microcentrifuge, and standard pipetting equipment. No specialized robotics, vacuum manifolds, or magnetic separation racks are needed. Choose a spin-column bacterial/fungal RNA kit for manual extraction of 1-24 samples per run, when existing automation infrastructure does not support magnetic bead formats, or when the fastest possible turnaround from culture to RT-qPCR data is required.

 

What you will find:

 

  • Pinpoint™ Slide RNA Isolation System for targeted extraction of total RNA directly from localized tissue sections on microscope slides

  • Quick-RNA™ Fungal/Bacterial MicroPrep Kit for highly concentrated, low-volume recovery of transcripts utilizing micro-elution spin-column matrices 

  • ZR Fungal/Bacterial RNA MiniPrep for precise cell-wall shattering of yeast and recalcitrant spores 

  • YeaStar™ RNA Kit efficiently permeabilizes tough yeast cell walls. 

 

How to Choose a Spin-Column Bacterial/Fungal RNA Kit

 

Miniprep vs. Microprep Format

The Zymo Quick-RNA Fungal/Bacterial Miniprep processes up to 2x10^8 bacteria or 2x10^7 fungi per column, eluting in 25-100 ul - the standard choice for typical 1-5 ml bacterial cultures. The Microprep handles smaller inputs (up to 1x10^7 bacteria) and elutes in as little as 6 ul, concentrating RNA for sensitive applications such as single-cell-equivalent samples or very low-input transcriptomics.

Bead Size for Target Organism

Pre-mixed 0.1 mm + 0.5 mm BashingBead tubes in Zymo kits handle bacteria (0.1 mm) and fungi (0.5 mm) without selecting bead size. For pure Gram-negative bacterial cultures that do not require bead beating, direct lysis in buffer is available as a faster protocol option that skips the bead-beating step entirely.

On-Column DNase I Treatment

Include DNase I for all RT-qPCR and RNA-seq applications. Bacterial gDNA is abundant and co-purifies efficiently under silica-membrane binding conditions; without DNase treatment, gDNA contamination produces false amplification in RT-qPCR assays targeting genes with no introns. DNase I Reaction Mix is included in Zymo Quick-RNA Fungal/Bacterial kits.

Elution Volume

Elute in 25-50 ul for standard RT-qPCR (2-5 ul per reaction provides 5-25 RNA equivalents per assay). For RNA-seq library preparation requiring >=200 ng input, use 50-100 ul elution volume to recover more total RNA mass; then measure concentration by Qubit and adjust for library prep.

Storage of Extracted RNA

Store spin-column bacterial RNA at -80C in single-use aliquots; mRNA from bacteria is AU-rich and degrades rapidly through multiple freeze-thaw cycles. Use within 6 months for transcriptomic applications; RT-qPCR targets with high expression levels remain quantifiable for 12+ months at -80C.

 

Specifications Context

 

Target quality metrics for spin-column bacterial/fungal RNA: A260/A280 >= 1.8, A260/A230 >= 1.5, and RIN >= 7 from log-phase cultures processed within 60 seconds of harvest. Zymo Research Quick-RNA Fungal/Bacterial kits use the same Zymo-Spin column technology found across the Quick-RNA product line and are validated for inhibitor-free RNA suitable for NGS, RT-PCR, microarray, and hybridization. The Quick-RNA Fungal/Bacterial Miniprep is one of the most widely used spin-column formats for bacterial and fungal RNA in academic molecular microbiology research, with validated protocols for S. cerevisiae, C. albicans, A. fumigatus, and standard Gram-positive and Gram-negative species. 

 

Contact the MBP team for kit selection guidance, bulk pricing, and Zymo Research protocol adaptation for non-standard organisms.

FAQ

Spin-column bacterial and fungal RNA extraction kits purify total RNA from Gram-positive bacteria, Gram-negative bacteria, yeast, filamentous fungi (Aspergillus, Candida, Neurospora), algae, and protozoa using ultra-high-density BashingBead mechanical lysis followed by silica-membrane spin-column purification in a standard microcentrifuge. The Zymo Research Quick-RNA Fungal/Bacterial Miniprep Kit completes extraction in minutes and yields inhibitor-free RNA ready for RT-qPCR, RNA-seq, and hybridization.
Use 0.1 mm BashingBeads for small Gram-positive and Gram-negative bacteria (E. coli, Staphylococcus); use 0.5 mm beads for yeast, filamentous fungi, and tough-walled organisms. Zymo Research Quick-RNA Fungal/Bacterial Lysis Tubes contain a pre-mixed combination of 0.1 mm and 0.5 mm beads, covering both bacteria and fungi in a single lysis tube without needing to select bead size by sample type.
The Zymo Quick-RNA Fungal/Bacterial Miniprep Kit completes lysis, spin-column binding, optional on-column DNase I treatment, wash, and elution in under 15 minutes for a batch of 1–12 samples when using a vortex adapter for bead beating. The Microprep format processes up to 700 µl of input in a single column; multiple columns can be loaded for larger input volumes.
Yes. Gram-negative bacteria (E. coli, Salmonella, Pseudomonas) can be lysed directly in Zymo RNA Lysis Buffer without mechanical homogenization, reducing protocol time by 5–8 minutes. However, Gram-positive species (Staphylococcus aureus, Bacillus subtilis, Listeria) and all fungi require bead beating at ≥4,000 rpm for complete cell wall disruption; skipping this step for tough-walled organisms produces low yields and poor A260/A230 ratios.
MBP carries the Zymo Research Quick-RNA Fungal/Bacterial Microprep Kit (up to 50 µl elution, ideal for concentrated samples or single-cell equivalents) and the Quick-RNA Fungal/Bacterial Miniprep Kit (larger binding capacity, 25–100 µl elution, suited for standard culture volumes). Both kits include ZR BashingBead Lysis Tubes with pre-loaded 0.1 mm and 0.5 mm beads and Zymo-Spin columns for inhibitor-free RNA purification.
On-column DNase I treatment is optional in Zymo Quick-RNA Fungal/Bacterial kits and requires a brief additional step using the supplied DNase I Reaction Mix. The step adds approximately 15 minutes to the protocol but is strongly recommended for RT-qPCR and RNA-seq applications, where gDNA contamination from bacterial genomes creates false-positive amplification signals and inflates expression measurements.
The Zymo Quick-RNA Fungal/Bacterial Miniprep Kit processes up to 2×10⁸ bacteria or 2×10⁷ yeast cells per extraction, with RNA yields of 5–50 µg depending on organism, growth phase, and culture volume processed. The Microprep format is designed for smaller inputs (up to 1×10⁷ bacteria) and elutes in as little as 6 µl for applications requiring high RNA concentration.
Bacterial RNA turns over rapidly; harvest cultures in late-log phase (OD₆₀₀ 0.4–0.8 for E. coli) and immediately transfer to Zymo DNA/RNA Shield, snap-freeze the pellet in liquid nitrogen, or proceed directly to lysis. Any delay between sample collection and lysis — even at 4°C — causes significant mRNA degradation. RNAprotect Bacteria Reagent (QIAGEN) can also be added directly to liquid cultures to stabilize RNA before pelleting.
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