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.
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| Packungsgröße | SKU | Verfügbarkeit | Preis |
|---|---|---|---|
| 10 reactions | Ab HEUTE lieferbarvonSchnelldorf | 43,70 € | |
| 50 reactions | Ab HEUTE lieferbarvonSchnelldorf | 191,00 € | |
| 250 reactions | Ab HEUTE lieferbarvonSchnelldorf | 855,00 € |
Über diesen Artikel
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.)
greener alternative product characteristics
Waste Prevention
Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
technique(s)
DNA purification: suitable
input
RNA
test parameters
: 3 min hands on time, sample volume: 90-110 μL
greener alternative category
, Aligned
storage temp.
room temp
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
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Dieser Artikel | |||
|---|---|---|---|
| technique(s) DNA purification: suitable | technique(s) DNA purification: suitable | technique(s) RNA purification: suitable | technique(s) DNA purification: suitable |
| storage temp. room temp | storage temp. room temp | storage temp. room temp | storage temp. 2-8°C |
| input RNA | input - | input DNA | input cells |
| purified by (Single-spin negative chromotography), (Time: 3 minutes or less) | purified by (Single-spin negative chromotography), (Time: 3 minutes or less) | purified by (Single-spin negative chromotography), (Time: 3 minutes or less) | purified by (Single-spin negative chromotography), (Time: 30 minutes or less) |
| test parameters : 3 min hands on time, sample volume: 90-110 μL | test parameters : 3 min hands on time, sample volume: 90-110 μL | test parameters : 3 min hands on time, sample volume: 90-110 μL | test parameters : 3 min hands on time |
| greener alternative product characteristics Waste Prevention | greener alternative product characteristics Waste Prevention | greener alternative product characteristics Waste Prevention | greener alternative product characteristics Waste Prevention |
Nur Kit-Komponenten
- Organic Solveent DNA Cleanup Spin Columns
- 1x Tris Buffer
Lagerklasse
10 - Combustible liquids
wgk
WGK 3
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Artikel
GenElute™-E DNA purification kits ensure accurate DNA quantitation and downstream enzymatic processes.
Auswirkungen der Aufreinigungsmethode auf die Genauigkeit der DNA-Quantifizierung und nachgeschaltete enzymatische Prozesse Bewertung der Reinheit genomischer DNA durch UV-Spektralphotometrie, Gelelektrophorese und nachgeschaltete qPCR bei Verwendung von GenElute™-E DNA-Aufreinigungskits.
Verwandter Inhalt
Animation showing technology principle of GenElute™-E single spin negative chromatography nucleic acid purification kits
Answers to frequently asked questions related to GenElute™-E single spin DNA and RNA purification and negative chromatography
Reduce plastic waste and eliminate hazardous liquid waste for more sustainable laboratories with GenElute™-E Single Spin DNA and RNA prep kits.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| EC700-250RXN | 04061842202829 |
| EC700-50RXN | 04061842202812 |
| EC700-10RXN | 04061842202805 |
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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 Antwort-
Hilfreich?
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Do we know how stable the purified DNA is through several freeze-thaw cycles?
1 Antwort-
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).
Hilfreich?
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What is the composition of the lysis buffer and clearing buffer after flowing through the resin?
1 Antwort-
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.
Hilfreich?
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Does the technology introduce any bias into the sample?
1 Antwort-
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.
Hilfreich?
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