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.
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 10 reactions | Please contact Customer Service for Availability | PLN 217.00 | |
| 50 reactions | Please contact Customer Service for Availability | PLN 941.00 | |
| 250 reactions | Please contact Customer Service for Availability | PLN 4,240.00 |
About This Item
purified by
(Single-spin negative chromotography), (Time: 3 minutes or less)
feature
Compatible Application (Suitable for most common downstream applications, including genotyping, PCR, and NGS), Intended use (For the removal of organic solvent traces from DNA solutions), Typical/expected yield (Varies by sample. Please reference user guide for more information.)
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technique(s)
DNA purification: suitable
input
RNA
test parameters
: 3 min hands on time, sample volume: 90-110 μL
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, Aligned
storage temp.
room temp
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This Item | ||
|---|---|---|
| storage temp. room temp | storage temp. - | storage temp. - |
| purified by (Single-spin negative chromotography) | purified by (Single-spin negative chromotography), (Time: 45 minutes or less) | purified by (Single-spin negative chromotography), (Time: 30 minutes or less) |
| feature Compatible Application (Suitable for most common downstream applications, including genotyping, PCR, and NGS) | feature Compatible Application (Suitable for most common downstream applications, including genotyping, PCR, and NGS), Intended use (For the purificiation of genomic DNA from human or animal tissue), Typical/expected yield (Varies by sample. Please reference user guide for more information.) | feature Compatible Application (Suitable for most common downstream applications, including genotyping, PCR, and NGS), Intended use (For the purification of genomic DNA from liquid blood samples), Typical/expected yield (Varies by sample. Please reference user guide for more information.) |
| greener alternative product characteristics Waste Prevention | greener alternative product characteristics Waste Prevention | greener alternative product characteristics Waste Prevention |
| sustainability Greener Alternative Product | sustainability Greener Alternative Product | sustainability Greener Alternative Product |
| greener alternative category , Aligned | greener alternative category | greener alternative category |
General description
GenElute™-E kits are based on the principle of negative chromatography, where impurities like salt, detergent, proteins and organic solvents are removed by the column material and the purified nucleic acid is collected in the flow-through in just one single centrifugation step. This convenient procedure enables a significantly faster purification of nucleic acid samples than standard bind-wash-elute procedures, with less handling, drastically reduced plastic consumable usage, and no use of hazardous materials like chaotropic salts or organic solvents.
With conventional methods, traces of chaotropic salt and ethanol are usually coeluted with these purification procedures, which often leads to inhibition of real-time PCR experiments. GenElute™-E kits do not contain any chaotropic salts, organic solvents or EDTA, resulting in improved performance in downstream applications such as PCR.
Because of the negative chromatography principle, there is no limitation to the amount of DNA that is cleaned up. Maximum sample volume is 100 μl. The purified nucleic acid is eluted in water and can immediately be used for downstream applications. A 1x TE Buffer, pH 8.5, is supplied to enable storage of samples.
Application
Features and Benefits
Preparation Note
Other Notes
Legal Information
Kit Components Only
- Organic Solveent DNA Cleanup Spin Columns
- 1x Tris Buffer
Storage Class
10 - Combustible liquids
wgk
WGK 3
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Articles
Zestawy do oczyszczania DNA GenElute™-E zapewniają dokładną kwantyfikację DNA i dalsze procesy enzymatyczne.
GenElute™-E DNA purification kits ensure accurate DNA quantitation and downstream enzymatic processes.
Related Content
Reduce plastic waste and eliminate hazardous liquid waste for more sustainable laboratories with GenElute™-E Single Spin DNA and RNA prep kits.
Demo video showing how to purify DNA and RNA GenElute™-E single spin nucleic acid purification kits
Answers to frequently asked questions related to GenElute™-E single spin DNA and RNA purification and negative chromatography
GenElute™-E Single Spin DNA and RNA purification technology enables rapid DNA and RNA extraction and purification from mammalian cells, blood, tissue, and plant tissue samples.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| EC700-50RXN | 04061842202812 |
| EC700-10RXN | 04061842202805 |
| EC700-250RXN | 04061842202829 |
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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-
Helpful?
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Does the technology introduce any bias into the sample?
1 answer-
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.
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).
Helpful?
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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.
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