ZymoBIOMICS DNA/RNA Miniprep Kit
- Unbiased Lysis: Efficient and unbiased lysis of microbes including Grampositive/negative bacteria, fungi, protozoans, and viruses from any sample (feces, soil, plant, water, biofilms, swabs, saliva, body fluids, etc.)
- Ultra-Pure: DNA and Total RNA (including small/micro RNAs) is inhibitor-free and ready for qPCR and microbiome measurements using Next-Gen Sequencing.
- High Sensitivity: Increased detection limit of very low abundance organisms.
|Equipment||Microcentrifuge, vortex, cell disrupter (recommended)|
|Purity||DNA and RNA is ready for Next-Gen sequencing, RTPCR, microarray, hybridization, etc. A260/A280, A260/A230: >1.8.|
|Sample Source||Bacterial, fungal, protozoan, algae, viral, mitochondrial, and host RNA is efficiently isolated from ≤ 200 mg of mammalian feces, ≤ 250 mg soil, ≤ 200 mg plant/seed, 50-100 mg (wet weight) fungal bacterial cells, biofilms, and water.|
|Size Range||DNA and Total RNA ≥17 nt|
|Yield||100 µg DNA/RNA (binding capacity), ≥50 µl (elution volume)|
DNA and RNA were coextracted from human and mouse stomach biopsy using the ZymoBIOMICS DNA/RNA kit for downstream 16S rRNA sequencing targeting the hypervariable region V4. Microbiota analysis revealed Firmicutes being more transcriptionally active than Bacteroidetes along with selective enrichment and depletion of specific bacteria in the stomach.Wurm, P et al. Qualitative and Quantitative DNA- and RNA-Based Analysis of the Bacterial Stomach Microbiota in Human, Mice, and Gerbils. mSystems. 2018.
Researchers used 16s rRNA gene sequencing to identify the microbial community in a sulfur-rich, low-temperature environment and showed not only the presence of sulfur oxidizing microbes but also aerobic Flavobacterium. The DNA was extracted from mineral precipitate using ZymoBIOMICS DNA/RNA.Trivedi, CB et al. Low-Temperature Sulfidic-Ice Microbial Communities, Borup Fiord Pass, Canadian High Artice. Frontiers in Microbiology. 2018.
The ZymoBIOMICS DNA/RNA kit was used for co-extraction from 0.22 μm nitrocellulose water filters preserved in DNA/RNA Shield as well as biofilm membranes. Metagenomic and metatranscriptomic sequencing showed decreased microbial diversity and load after microfiltration and reverse osmosis. Water treatment also reduced the presence of antibiotic resistance genes and viruses.Stamps, BW et al. Characterization of the Microbiome at the World’s Largest Potable Water Reuse Facility. Frontiers in Microbiology. 2018.