Highlights
- Rapid, high-throughput (96-well) method 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.
- Zymo-Spin plate unique filtration technologies effectively removes PCR inhibitors from the DNA product.
Description
| Applicable For | All sensitive downstream applications such as qPCR and Next-Generation Sequencing. |
|---|---|
| Elution Volume | ≥ 50 µl |
| Equipment | Centrifuge w/ microplate carriers, 96-well plate/block disruptor or pulverizer. |
| Processing Volume | ≤80mg feces, ≤ 135 mg soil, ≤20 mg fungal/bacterial cells (wet weight) |
| Purity | A260/A280 nm ≥1.8. |
| Sample Source | Feces or soil |
| Sample Storage | DNA stored at ≤ -20°C. |
| Size Range | 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. |
| Type | Total DNA |
| Yield | ≤ 5 µg total DNA |
Q1: My lysate seems viscous. What is causing this to happen? How can I fix this?
A viscous sample can indicate incomplete sample lysis. Try using less of your sample and optimize bead beating conditions (duration, speed, time) to ensure samples are thoroughly lysed. After bead beating, pellet the cell debris before moving on. Adding more Genomic Lysis buffer to the lysate can help dilute and deproteinate the sample, making the sample less viscous and more suitable for DNA recovery.
Q2: What is the purpose of Silicon-A-HRC Plate step?
Environmental samples often contain inhibitors such as polyphenolics, humic/fulvic acids, tannins, melanins, etc. that affect downstream applications such as PCR. Once the DNA is eluted off the binding spin plate, the DNA is then passed through the Silicon-A-HRC Plate to remove the PCR inhibitors, and the DNA is then ready for downstream applications. The Silicon-A-HRC Plate does not bind DNA, it simply removes the PCR inhibitors. The Silicon-A-HRC Plate can be purchased separately as the OneStep-96 PCR Inhibitor Kit (D6035).
Q3: Is it necessary to add beta-mercaptoethanol? Can this step be substituted or omitted?
Addition of beta-mercaptoethanol is recommended to enhance sample lysis, but can be substituted with dithiothreitol (DTT, final concentration of 10 mM). However, if bead beating is optimized and lysis is efficient, the addition of BME is not necessary and can be omitted.
Q4: When can an RNase A treatment be implemented in the protocol?
No additional RNase A treatment is required when processing samples within kit capacity. The selective chemistry allows for binding of double stranded DNA to the column and for RNA to flow through.
| Cat # | Name | Size | Price | |
|---|---|---|---|---|
| S6002-96-3 | ZR-96 BashingBead Lysis Rack | 0.5 mm & 0.1 mm | $192.00 | |
| C2009 | Silicon-A-HRC Plate | 2 Plates | $405.00 | |
| C2003 | Elution Plate | 2 Plates | $19.00 | |
| C2002 | Collection Plate | 2 Plates | $22.00 | |
| C2007-4 | 96-Well Plate Cover Foil | 4 Foils | $10.00 | |
| P1001-2 | 96-Well Block | 2 Blocks | $18.00 | |
| C2001 | Silicon-A Plate | 2 Plates | $129.00 | |
| D6035-1-30 | Prep Solution | 30 ml | $18.00 | |
| D6001-3-40 | BashingBead Buffer | 40 ml | $29.00 | |
| D3004-5-50 | DNA Pre-Wash Buffer | 50 ml | $26.00 | |
| D3004-4-10 | DNA Elution Buffer | 10 ml | $14.00 | |
| D3004-2-100 | g-DNA Wash Buffer | 100 ml | $30.00 | |
| D3004-1-150 | Genomic Lysis Buffer | 150 ml | $73.00 |
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