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 | Warenkorb auf Verfügbarkeit prüfen | CHF 46.90 | |
| 50 reactions | Warenkorb auf Verfügbarkeit prüfen | CHF 192.00 | |
| 250 reactions | Warenkorb auf Verfügbarkeit prüfen | CHF 862.00 |
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 depletion of impurities and partial fractions (<50 bp) from DNA solutions), Typical/expected yield (Varies by sample. Please reference user guide for more information.)
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Designing Safer Chemicals
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sustainability
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technique(s)
DNA purification: suitable
test parameters
: 3 min hands on time, sample volume: 90-110 μL
greener alternative category
storage temp.
room temp
General description
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 |
| 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 |
| sustainability Greener Alternative Product | sustainability Greener Alternative Product | sustainability Greener Alternative Product | sustainability Greener Alternative Product |
| 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) |
| greener alternative category | greener alternative category , Aligned | greener alternative category | greener alternative category |
| storage temp. room temp | storage temp. room temp | storage temp. room temp | storage temp. 2-8°C |
Nur Kit-Komponenten
- DNA Cleanup Spin Columns
- 1x Tris Buffer
Lagerklasse
10 - Combustible liquids
wgk
WGK 3
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Artikel
Impatto del metodo di purificazione sull'accuratezza della quantificazione del DNA e sulle procedure enzimatiche successive. Valutazione mediante spettrofotometria UV, elettroforesi su gel e successiva qPCR della purezza del DNA genomico purificato con i kit GenElute™-E.
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.
GenElute™-E DNA purification kits ensure accurate DNA quantitation and downstream enzymatic processes.
Verwandter Inhalt
Major technological advances have made the production of monoclonal antibodies quicker and more efficient. There are three established platforms for antibody discovery. We offer reagents for production of monoclonal antibody libraries using each of these techniques.
Risposte alle domande frequenti in merito al metodo GenElute™-E per la purificazione di DNA e RNA con un’unica centrifugazione grazie alla cromatografia negativa
I kit GenElute™-E per la purificazione del DNA e dell'RNA con un’unica centrifugazione aiutano a ridurre il consumo di plastica ed eliminano gli scarti di liquidi pericolosi, migliorando così l’impronta ambientale del laboratorio.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| EC600-50RXN | 04061842202782 |
| EC600-250RXN | 04061842202799 |
| EC600-10RXN | 04061842202775 |
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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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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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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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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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