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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| 10 reactions | Veuillez contacter notre Service Clients pour connaître la disponibilité de ce produit. | 43,60 € | |
| 50 reactions | Veuillez contacter notre Service Clients pour connaître la disponibilité de ce produit. | 190,00 € | |
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A propos de cet article
43,60 €
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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sustainability
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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
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Cet article | |||
|---|---|---|---|
| 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 |
Composants de kit seuls
- Organic Solveent DNA Cleanup Spin Columns
- 1x Tris Buffer
Classe de stockage
10 - Combustible liquids
wgk
WGK 3
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Articles
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.
Impact de la méthode de purification sur l'exactitude de la quantification de l'ADN et les procédés enzymatiques en aval. Évaluation de la pureté de l'ADN génomique par spectrophotométrie UV, électrophorèse sur gel et qPCR en aval à l'aide des kits de purification d'ADN GenElute™-E.
Contenu apparenté
Antworten auf häufig gestellte Fragen (FAQ) zur GenElute™-E Einzel-Spin DNA-/RNA-Aufreinigung und Negativ-Chromatographie
Mit den GenElute™-E Einzel-Spin DNA- und RNA-Prep-Kits kann/können Plastikmüll reduziert und gefährliche Flüssigabfälle vermieden werden, um die Nachhaltigkeit im Labor zu verbessern.
Animation showing technology principle of GenElute™-E single spin negative chromatography nucleic acid purification kits
Numéro d'article de commerce international
| Référence | 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 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.
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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.
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