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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| Talla/SKU | Disponibilidad | Precio |
|---|---|---|
10 reactions | Póngase en contacto con nuestro Servicio de Atención al Cliente para disponibilidad | 39,60 € |
50 reactions | Póngase en contacto con nuestro Servicio de Atención al Cliente para disponibilidad | 175,00 € |
250 reactions | Póngase en contacto con nuestro Servicio de Atención al Cliente para disponibilidad | 777,00 € |
Acerca de este artículo
39,60 €
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 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
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storage temp.
room temp
General description
Application
Features and Benefits
Preparation Note
Other Notes
Legal Information
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Este artículo | ||
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| description Reagents and consumables for clean-up of pre-purified DNA. 10, 50 or 250 purifications. | description Reagents and consumables for organic solvent clean-up from DNA. 10, 50 or 250 purifications. | description Reagents and consumables for various tissue sample types. 96-well plate format. |
| technique(s) DNA purification: suitable | technique(s) DNA purification: suitable | technique(s) - |
| sustainability Greener Alternative Product | sustainability Greener Alternative Product | sustainability Greener Alternative Product |
| greener alternative category | greener alternative category , Aligned | greener alternative category , Aligned |
| feature Typical/expected yield (Varies by sample. Please reference user guide for more information.), 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) | 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.) | feature Typical/expected yield (Varies by sample. Please reference user guide for more information.), 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) |
| purified by (Single-spin negative chromotography), (Time: 3 minutes or less) | purified by (Time: 3 minutes or less), (Single-spin negative chromotography) | purified by (Single-spin negative chromotography) |
| storage temp. room temp | storage temp. room temp | storage temp. 2-8°C |
Solo componentes del kit
- DNA Cleanup Spin Columns
- 1x Tris Buffer
Clase de almacenamiento
10 - Combustible liquids
wgk
WGK 3
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Does the technology introduce any bias into the sample?
1 respuesta-
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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 respuesta-
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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What is the composition of the lysis buffer and clearing buffer after flowing through the resin?
1 respuesta-
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 respuesta-
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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