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DNeasy PowerMax Soil Kit

For the isolation of microbial DNA from large quantities of soil with low microbial load
  • Short isolation time of highly pure DNA from up to 10 g soil in 30 minutes
  • High-quality DNA recovery from low biomass samples from large sample quantities
  • Efficient elimination of humic substances and PCR inhibitors using Inhibitor Removal Technology
  • High-quality DNA that is ready to use in downstream applications    

Biodensity of a soil or other environmental sample is not a problem when using the DNeasy PowerMax Soil Kit. This kit, designed for processing large sample quantities, will give researchers DNA samples free from PCR inhibiting compounds generally associated with soil DNA. Humic substances and the color from compost, manure and sediment are eliminated through Inhibitor Removal Technology. Resulting DNA is ready to use in a variety of downstream applications such as qPCR, Sanger sequencing and next-generation sequencing. Want to try this solution for the first time? Request a quote for a trial kit.

DNeasy PowerMax Soil Kit was formerly sold by MO BIO as PowerMax Soil DNA Isolation Kit.

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Cat No./ID: 12988-10
DNeasy PowerMax Soil Kit (10)
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For the isolation of microbial DNA from large quantities of soil with low microbial load
The DNeasy PowerMax Soil Kit is intended for molecular biology applications. This product is not intended for the diagnosis, prevention, or treatment of a disease.

Product Details

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Figure 3. DNeasy PowerMax Soil Kit isolated total genomic DNA.
One µl was amplified using primers to the Streptococcus spp. 1% TAE agarose and ethidium staining was used to analyze the DNA. Quantity of PCR fragmentation in each sample is relative to that in the template sequence in the purified DNA. Genomic DNA from different sample sources contains variability due to types and quantity of organisms in the respective soils. N = Negative control lacking template. P = Positive control template.
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Figure 2. More amplified DNA across soil types.
PCR was used to amplify 1 µl of total genomic DNA isolated using primers to the Bacillus spp. Analysis on the amplified DNA used 0.8% TAE agarose and ethidium staining. Quantity of PCR fragmentation in each sample is relative to that in the template sequence in the purified DNA. Genomic DNA from different sample sources contains variability due to types and quantity of organisms in the respective soils. N = Negative control lacking template. P = Positive control template.
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Figure 1. Total genomic DNA isolated from any soil type.
The DNeasy PowerMax Soil Kit was used to isolate total genomic DNA from 8 different soil samples. Isolated DNA (0.75 µg of each) was ethidium stained and analyzed on a 1% TAE agarose gel. M = Marker DNA.
Performance



Specifications

Features
Specifications
Bead size 0.7 mm garnet
Binding capacity Up to 1 mg per filter
Format Silica Spin Filter Tubes
Processing Bead beating
Sample size Up to 10 g
Sample types Processed soil, stool, gut material, biosolids
Storage temperature Store at room temperature(15-30°C)
Throughput 2 samples
Time per run or per prep 30 minutes

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