Product Filters

Environmental RNA Kits for Soil, Water, and Biofilm

 

Environmental RNA extraction kits isolate total RNA from soil, sediment, water concentrates, biofilm, feces, and plant material for metatranscriptomic profiling of active microbial communities. Specialized inhibitor-removal chemistry and bead-beating lysis address the humic acids, polyphenols, and polysaccharides that co-extract from environmental matrices and block downstream RT-PCR and sequencing.

MBP carries Zymo Research Quick-RNA Fecal/Soil Microbe kits and ZymoBIOMICS DNA/RNA formats for paired metatranscriptomic and metagenomic workflows, available to registered vendors including Howard Hughes Medical Institute, Vanderbilt University, and MD Anderson Cancer Center. Request a quote today by contacting customerservice@mbpinc.net.

Environmental

Per Page:
Sort By:
ZR Soil/Fecal RNA MicroPrep (50 Preps.)
List Price:
USD167.58 - USD551.95
Online Price:
USD119.70 - USD394.25
Your Price:
ZR Urine RNA Isolation Kit™
List Price:
USD49.21 - USD469.49
Online Price:
USD35.15 - USD335.35
Your Price:
Zymo Environ Water RNA Kit (50 preps)
List Price:
USD10.64 - USD638.40
Online Price:
USD7.60 - USD456.00
Your Price:

Showing 1 to 3 of 3 results

What are Environmental RNA Extraction Kits?

 

Environmental RNA (eRNA) extraction kits isolate total RNA from complex non-cellular matrices - soil, sediment, water, biofilm, fecal material, plant tissue, and air filter samples - for use in metatranscriptomic profiling of active microbial community gene expression. Unlike RNA kits designed for pure cultures or tissue, environmental RNA kits incorporate specialized bead-beating lysis, inhibitor co-precipitation, and sequential wash steps to remove the humic acids, polyphenols, and polysaccharides that co-extract from environmental matrices and inhibit downstream RT-PCR and RNA-seq workflows. Use an environmental RNA kit - not a standard total RNA or microbial RNA kit - whenever your sample is soil, sediment, water concentrate, biofilm, or feces, where co-purified inhibitors are the primary obstacle to usable RNA.

 

What you will find:

 

Spin-column:

 

  • Zymo Environ Water RNA and ZR Soil/Fecal RNA MicroPrep systems for purification of total RNA from environmental and microbiome samples.
  • Spin-column extraction technologies designed to recover high-quality RNA from water, soil, sediment, and fecal specimens.
  • Inhibitor-removal workflows that help eliminate humic acids and other contaminants common in environmental samples.
  • RNA isolation solutions optimized for downstream RT-PCR, qPCR, sequencing, and microbial gene expression studies.
  • Research-grade purification systems that support environmental monitoring, microbiome analysis, and metatranscriptomics applications.

 

How to Choose an Environmental RNA Extraction Kit

 

Soil Type and Inhibitor Load

High-organic-matter soils (peat, forest soils) carry more humic acid inhibitors than low-organic sandy soils. A 2024 peer-reviewed comparison published in Microbiology Society Journals found the QIAGEN RNeasy PowerSoil Total RNA Kit outperformed competing products across diverse soil types for long-read metatranscriptomics, delivering superior RNA integrity and yield. The Zymo Quick-RNA Fecal/Soil Microbe Microprep Kit is faster (approximately 2 hours) and provides a higher throughput option suited for lower-humic or fecal samples.

DNA Co-Extraction

For paired DNA/RNA metatranscriptomics from the same environmental sample, select a kit validated for co-extraction, such as the Zymo ZymoBIOMICS DNA/RNA Miniprep Kit. Processing both analytes from the same physical sample reduces extraction variability and sample volume requirements - important when sample mass is limiting, as in microdissected biofilms or filtered water aliquots.

Sample Input Amount

Standard environmental RNA kits accept 0.1-0.5 g of soil or feces per extraction; exceeding this limit overloads the inhibitor-removal chemistry and silica membrane. For samples with very low microbial biomass (e.g., subsoil, oligotrophic water), pool multiple extractions and concentrate using an RNA Clean & Concentrator kit before downstream assays.

rRNA Depletion Compatibility

Confirm that the extracted RNA is compatible with your rRNA depletion method. Residual inhibitors from soil RNA extractions can impair enzymatic depletion reactions; a cleanup or concentration step between extraction and depletion improves performance. The Zymo RNA Clean & Concentrator-5 kit is commonly used for this purpose.

Speed vs. RNA Quality Trade-off

The Zymo Fecal/Soil kit completes extraction in approximately 2 hours with mini-spin columns and provides higher throughput; the QIAGEN PowerSoil kit takes 5-7 hours, including optional incubation steps, but delivers superior RNA integrity for long-read sequencing applications requiring intact RNA molecules longer than 500 nt.

 

Specifications Context

 

RNA quality targets from environmental extractions: A260/A280 >= 1.8, A260/A230 >= 1.5 (lower ratios indicate inhibitor carryover), and RIN >= 5 for metatranscriptomics. Soil metatranscriptomics is an active area of environmental microbiology - with applications in carbon cycling research, agricultural soil health assessment, and bioremediation monitoring - and RNA extraction quality is a primary bottleneck cited in published workflows. For long-read sequencing (Oxford Nanopore direct RNA sequencing), RIN >= 7 and RNA concentration >= 20 ng/ul are required; this requirement makes kit selection and inhibitor removal more critical for long-read than for short-read workflows.

 

Contact the expert team at MBP Inc. today and get high-purity environmental RNA extraction purification systems for your lab.

FAQ

Environmental RNA (eRNA) extraction kits isolate total RNA from complex non-cellular matrices — soil, water, sediment, biofilm, feces, plant material, and air filter samples — used in metatranscriptomic studies of active microbial community gene expression. Unlike RNA kits designed for pure cultures or tissue, environmental RNA kits incorporate co-purification inhibitor removal steps to address the humic acids, polyphenols, polysaccharides, and heavy metals that co-extract from environmental matrices and inhibit downstream enzymatic assays.
Environmental samples contain high concentrations of co-purified PCR inhibitors — humic acids in soil, tannins in plant material, and complex organic polymers in biofilm — that bind to silica membranes and inhibit RT-qPCR enzymes. Additionally, microbial RNA turnover in environmental samples is rapid; RNA degrades within seconds to minutes at room temperature without stabilization. Environmental RNA kits address both challenges with specialized inhibitor-removal wash steps and chaotropic lysis buffers that simultaneously inactivate RNases at the point of disruption.
Zymo Research Quick-RNA Fecal/Soil Microbe Microprep Kit processes soil (0.1–0.25 g), fecal material, water (after concentration), biofilm, plant tissue, and agricultural samples. QIAGEN RNeasy PowerSoil Total RNA Kit is optimized for high-humic-content soils across multiple soil types. Norgen Soil Total RNA Purification Kit accepts soil samples from 0.1–0.25 g per extraction. Confirm the kit's validated sample list against your specific matrix before purchasing.
Environmental RNA kits remove PCR inhibitors through sequential wash steps using specialized buffers targeting humic acids and polyphenols, PowerBead bead beating to release RNA and denature inhibitors simultaneously, in-column precipitation steps that selectively precipitate polysaccharides, and phenol-chloroform clearing of lipids and proteins in protocol variants requiring higher purity. The RNeasy PowerSoil Total RNA Kit uses a proprietary Inhibitor Removal Technology (IRT) step validated across diverse soil types.
Typical total RNA yields from 0.25 g of agricultural soil range from 500 ng to 5 µg depending on soil microbial biomass, organic matter content, and extraction protocol. High-organic-matter soils yield more RNA but also more co-purified inhibitors. The QIAGEN RNeasy PowerSoil Total RNA Kit was shown in a 2024 peer-reviewed comparative study to deliver the highest RNA yield and quality from soil across multiple kit comparisons for long-read metatranscriptomics.
Aquatic environmental RNA from water samples requires a concentration step before extraction — filtration through 0.2–0.45 µm sterivex or membrane filters to capture microbial biomass, followed by elution of cells from the filter into an RNA lysis buffer. Zymo Research Quick-RNA Fecal/Soil Microbe Microprep Kit processes the resulting cell pellet or filter eluate. For large water volumes (1–10 L), Sterivex filtration followed by direct in-filter lysis with RNA buffer is the most widely used approach.
Yes, for metatranscriptomic RNA-seq. Ribosomal RNA (rRNA) constitutes 85–97% of total RNA from environmental microbial communities; without depletion, mRNA signals from active genes are overwhelmed by rRNA reads in sequencing data. After extraction, add a prokaryotic or pan-microbial rRNA depletion step using a Zymo-Seq RiboFree Total RNA Library Kit or a ribodepletion bead kit before library preparation.
Soil and fecal samples should be snap-frozen in liquid nitrogen within minutes of collection and stored at -80°C for maximum RNA integrity. For field settings without liquid nitrogen access, Zymo DNA/RNA Shield added directly to the sample tube at a 1:1 ratio immediately after collection preserves RNA at ambient temperature for up to 30 days, enabling room-temperature transport from remote sites. Water filter samples should be frozen at -80°C immediately or stored in RNAlater for short-term stabilization.
We provide the highest quality of products and anytime customer service.
Featured Categories
    online payment
    online payment
    fast delivery
    fast delivery
    technical support
    technical support
    24/7 support
    24/7 support
    copy right
    2026 All Right Reserved