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Invitrogen™ PureLink™ Microbiome DNA Purification Kit
Description
The Invitrogen™ PureLink™ Microbiome DNA Purification Kit uses proven PureLink™ spin column technology for robust yields of purified DNA ready for downstream PCR, sequencing or other applications. The highly efficient triple lysis approach, fast removal of inhibitors, and versatility makes PureLink the ultimate kit for microbiome research projects as well as programs aimed at rapid detection of pathogenic bacteria in various samples.
- Efficient lysis of all microorganisms (including durable species with thicker and more complex cell walls) by a combination of heat, chemical, and mechanical disruption with specialized beads
- Elimination of inhibitory compounds by precipitation using a novel cleanup buffer
- Streamlined protocols for numerous biological samples
- Recovery of highly pure DNA compatible with common downstream applications such as qPCR and next-generation sequencing
Certifications
Certificates of Analysis for each lot
Warranty and Services
Product performance guaranteed for 1 year from date of sale
Specifications
Specifications
| Column Type | Spin Column |
| Content And Storage | • 40 mL S1 Lysis Buffer; room temperature • 5 mL S2 Lysis Enhancer; room temperature • 12.5 mL S3 Cleanup Buffer; room temperature • 45 mL S4 Binding Buffer; room temperature • 13 mL S5 Wash Buffer (concentrated); room temperature • 5 mL S6 Elution Buffer; room temperature • 50 PureLink Columns with Collection Tubes; room temperature • 100 PureLink Collection Tubes; room temperature • 50 Bead Tubes; room temperature |
| Isolation Technology | Silica Spin Column |
| Scale | Mini |
| Sample Type | Microbial Culture, Saliva, Soil, Stool, Host DNA from Stool, Swabs (Buccal, Vaginal, Skin, Rectal, or Environmental), Cells, Food and Environmental |
| Elution Volume | 50 to 200 μL |
| Final Product Type | Microbial and host DNA |
| For Use With (Application) | PCR, Southern blotting, sequencing, nucleic acid labeling, hybridization |
| High-throughput Compatibility | Not High-throughput Compatible (Manual) |
| Quantity | 50 Preps kit |
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Frequently Asked Questions (FAQs)
The swab should be removed after incubation, prior to bead beating.
Yes, the elution buffer in the PureLink Microbiome DNA Purification Kit contains EDTA. An alternative that does not contain EDTA is Tris Buffer (10 mM Tris-HCl, pH 8.0-9.0). Eluting in water is possible, but the low pH of water could lead to reduced stability and less accurate OD readings.
For some samples, including soil and stool samples, it can be difficult to withdraw 400 µL supernatant while avoiding debris. If less than 250 µL of supernatant is transferred, add S1-Lysis buffer to bring the volume to 400 µL, before adding S3-Cleanup Buffer.
Low yield could be caused by inefficient lysis and/or low levels of DNA in the sample. Please try heating samples at 95 degrees C for 5-10 minutes instead of 65 degrees C for 10 minutes after adding S2-Lysis Enhancer. Bead beat for a longer time or at a higher power setting. You can also try to perform the experiment with more starting material, but do not exceed what we specify in the protocol. However for some challenging samples, too much starting material can also result in low yield. In this case, please try less starting material and/or increase the volume of S1-Lysis Buffer.
There are several options to rescue your DNA obtain good PCR results including diluting your DNA sample, using specific enzymes, and/or using an additive. The methods are described below:
- Dilute your DNA sample 10-100 times prior to PCR which will dilute out the contaminants while the PCR signal in many cases will remain strong.
- Use tough enzymes that were specifically designed and optimized to be effective in harsh environments, and work in the presence of high levels of inhibitors, for instance, TaqPath qPCR Master Mix, CG Reagent.
- Use a BSA additive for the PCR reaction. In most cases, if used at appropriate concentration, BSA can rescue your sample.
You can also try repeating the purification with less starting material or increased volume of S1-Lysis buffer. Additionally, after the addition of the S3- Cleanup buffer, you can try incubating the sample for 10 minutes on ice before centrifugation.
Safety and Handling
For research use only. Not for use in diagnostic procedures.
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