ZR Fecal DNA MicroPrep™

Rapid methods for the isolation of inhibitor-free, PCR-quality DNA from fecal samples in minutes including those from humans, birds, rats, mice, cattle, etc.
Ultra-high density BashingBeads™ are fracture resistant and chemically inert.
Fast-Spin column and unique filtration technologies effectively removes PCR inhibitors from the DNA product.

Product Name Size Catalog # Price Qty
ZR Fecal DNA MicroPrep™ 50 Preps. D6012
$192.00

About ZR Fecal DNA MicroPrep™

The ZR Fecal DNA MicroPrep™ is designed for the simple and rapid isolation of inhibitor-free, PCR-quality host cell and microbial DNA from a variety of sample sources including humans, birds, rats, mice, cattle, etc. The procedure is easy and can be completed in minutes: fecal samples are rapidly and efficiently lysed by bead beating with our state of the art, ultra-high density BashingBeads™. Fast-Spin column technology is then used to isolate the DNA which is subsequently filtered to remove humic acids/polyphenols that can inhibit PCR. Eluted DNA is ideal for downstream molecular-based applications including PCR, arrays, genotyping, methylation detection, etc.

Specifications

Format Spin Column
DNA Recovery Up to 5 μg total DNA is eluted into ≥ 10 μl DNA Elution Buffer per sample.
Processing Time 15 min
Equipment Microcentrifuge, vortex, cell disruptor/pulverizer (optional)
DNA Size Limits Capable of recovering genomic DNA up to and above 40 kb. In most instances, mitochondrial DNA and viral DNA (if present) will also be recovered.
Sample Sources Bacterial, protist, as well as host DNA can be effectively isolated from a ≤150 mg sample of mammalian feces.
DNA Purity High quality, inhibitor-free DNA is eluted with DNA Elution Buffer suitable for the amplification of bacterial, protist, and/or mammalian templates. A260/A280 >1.8

Comparison of DNA yields from rat feces using the ZR Fecal DNA MiniPrep™ and kits from suppliers A and B. Equivalent amounts of feces were processed using each kit and then equal volumes of eluted DNA were analyzed in a 0.8% (w/v) agarose/ethidium bromide gel. Samples were processed in triplicate.