GenElute™-E does not introduce biases that some “bind-wash-elute” technologies can add because the technology separates by size, rather than by what binds and what is released.
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Quality Level
technique(s)
DNA purification: suitable, RNA purification: suitable
input
sample(s) (swabs: nasopharyngeal and genital)
sample(s) (stool)
test parameters
: 3 min hands on time, sample volume: 10-20 mg stool, sample volume: 50 μL swabs
storage temp.
2-8°C
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Este artículo | |||
|---|---|---|---|
| input DNA | input DNA | input DNA | input RNA |
| storage temp. 2-8°C | storage temp. 2-8°C | storage temp. 2-8°C | storage temp. room temp |
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level 100 |
General description
- Isolation of viral RNA and DNA in less than 30 minutes with minimal sample handling
- Better purity, leading to improved performance in PCR and other applications
- Significant reduction in plastic and hazardous chemical waste
Traditional silica-based, bind-wash-elute purification kits require multiple wash steps to remove impurities from the spin columns. These steps increase the risk of cross contamination, and subject the nucleic acids to centrifugation sheering forces.
GenElute™-E kits employ size exclusion negative chromatography to separate large nucleic acid molecules from smaller protein, lipid, and ionic components in swab, cell, tissue, blood, and other samples. Single-spin columns efficiently absorb and retain cellular debris and sample contaminantswhile allowing nucleic acids to pass through, reducing the number of steps and plastic materials required for purification. This novel method for high-qualitypurification is made possible by our innovative SmartLyse® Buffer, which enables fast and efficient isolation.
Isolate nucleic acid in a fraction of time compared to traditional silica bind-wash-elute procedures. Simply prepare spin column, mix sample with lysis components, pipette sample onto the spin column, and centrifuge directly into a collection tube. Cellular debris and contaminants remain bound in the column to be discarded, while purified viral RNA and DNA is ready to be used in downstream applications or stored.
Application
The sample lysis utilizes the SmartLyse® Viral Buffer for fast and efficient isolation of nucleic acids from a variety of swab types and stool samples.
Purified viral RNA and DNA is eluted in Tris buffer, pH 7.8 and can immediately be used for most common downstream applications, including PCR, genotyping, NGS, and others. Final yield is comparable to most common silica-based methods. GenElute™-E purified genomic DNA preparations commonly show an A260/280 ratio of around 1.8.
Features and Benefits
- Fast and efficient purification: no lysis incubation and minimal hands-on, preparation steps
- Higher quality nucleic acids: negative chromotography-based purification reduces carryover of PCR inhibitors and other contaminents
- Reduced environmental impact: 55% less plastic waste, as well as a significant reduction in hazardous chemicals
Other Notes
Legal Information
Solo componentes del kit
- SmartLyse® Viral Buffer
- GenElute™-E Spin Columns
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Artículos
GenElute™-E DNA purification kits ensure accurate DNA quantitation and downstream enzymatic processes.
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Does the technology introduce any bias into the sample?
1 answer-
Helpful?
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Do we know how stable the purified DNA is through several freeze-thaw cycles?
1 answer-
This will fluctuate due to sample variability (sample collection, concentration, fragment length, sequence [GC content], storage before isolation, etc.). However, the sample is buffer exchanged into a standard storage buffer that is included in the kit (1X TE).
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What is the composition of the lysis buffer and clearing buffer after flowing through the resin?
1 answer-
The presence of EDTA, SDS, or excess salt can affect my PCR/ sequencing reaction. The lysis buffer information is proprietary, but we can say it is free of chaotropic salts. The resins are desalting resins so EDTA, SDS, and salts are depleted.
Helpful?
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Genelute-e single spin DNA and RNA purification kits use negative chromatographty to isolate nucleic acids. Can you explain how this approach simplifies workflows?
1 answer-
Instead of optimizing the bind, wash, and release steps in conventional silica-based spin purification preps, the technology focuses on a separation by performing a single step fractionation based on the size of the biomolecules, which results in depleted impurities.
Helpful?
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