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 | Vérifier la disponibilité des articles du panier | 39,50 € | |
| 50 reactions | Vérifier la disponibilité des articles du panier | 175,00 € | |
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A propos de cet article
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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Waste Prevention
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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Cet article | |||
|---|---|---|---|
| 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 |
Composants de kit seuls
- DNA Cleanup Spin Columns
- 1x Tris Buffer
Classe de stockage
10 - Combustible liquids
wgk
WGK 3
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Articles
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.
Contenu apparenté
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.
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.
Animation montrant le principe de fonctionnement des kits de purification d'acides nucléiques par chromatographie négative en une seule centrifugation GenElute™-E
Numéro d'article de commerce international
| Référence | 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 réponse-
Utile ?
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What is the composition of the lysis buffer and clearing buffer after flowing through the resin?
1 réponse-
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.
Utile ?
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Do we know how stable the purified DNA is through several freeze-thaw cycles?
1 réponse-
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).
Utile ?
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Does the technology introduce any bias into the sample?
1 réponse-
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.
Utile ?
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