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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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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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
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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 organic solvent clean-up from RNA. 10, 50 or 250 purifications. | description Reagents and consumables for various cell culture sample types. 10, 50 or 250 purifications. |
| technique(s) DNA purification: suitable | technique(s) DNA purification: suitable | technique(s) RNA purification: suitable | technique(s) DNA purification: suitable |
| greener alternative category | greener alternative category , Aligned | greener alternative category | greener alternative category |
| feature Compatible Application (Suitable for most common downstream applications, including genotyping, PCR, and NGS), Typical/expected yield (Varies by sample. Please reference user guide for more information.), 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 Compatible Application (Suitable for most common downstream applications, including RT-PCR, gene expression, and NGS), Intended use (For depletion of impurities from RNA solutions), Typical/expected yield (Varies by sample. Please reference user guide for more information.) | feature Compatible Application (Suitable for most common downstream applications, including genotyping, PCR, and NGS), Intended use (For purification of genomic DNA from cell lines), Typical/expected yield (Varies by sample. Please reference user guide for more information.) |
| 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
- DNA Cleanup Spin Columns
- 1x Tris Buffer
Lagerklasse
10 - Combustible liquids
wgk
WGK 3
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Does the technology introduce any bias into the sample?
1 answer-
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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-
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 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).
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