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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purified by
(Single-spin negative chromotography), (Time: 30 minutes or less)
feature
Compatible Application (Suitable for most common downstream applications, including genotyping, PCR, and NGS), Intended use (For the purification of genomic DNA from liquid blood samples), Typical/expected yield (Varies by sample. Please reference user guide for more information.)
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Waste Prevention
Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.
sustainability
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technique(s)
DNA purification: suitable
input
blood (liquid or dried)
test parameters
: 3 min hands on time, sample volume: 200-1000 μL blood
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storage temp.
2-8°C
Categorie correlate
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| purified by (Single-spin negative chromotography) | purified by (Single-spin negative chromotography), (Time: 45 minutes or less) | purified by - | purified by - |
| feature Compatible Application (Suitable for most common downstream applications, including genotyping, PCR, and NGS) | feature 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), Typical/expected yield (Varies by sample. Please reference user guide for more information.) | feature - | feature - |
| greener alternative product characteristics Waste Prevention | greener alternative product characteristics Waste Prevention | greener alternative product characteristics - | greener alternative product characteristics - |
| sustainability Greener Alternative Product | sustainability Greener Alternative Product | sustainability - | sustainability - |
| greener alternative category | greener alternative category | greener alternative category - | greener alternative category - |
General description
- Isolation of DNA in under an hour with minimal sample handling
- Better purity, leading to improved performance in PCR and other applications
- Significant reduction in plastic and hazardous chemical waste
Traditional silica-based, bind-wash-elute purification kits require multiple wash steps to remove impurities from the spin columns. These steps increase the risk of cross contamination, subject the DNA to centrifugation sheering forces, and introduce chaotropic salts that can carry over into the final sample, inhibiting downstream applications.
GenElute™-E kits employ size exclusion negative chromatography to separate large nucleic acid molecules from smaller protein, lipid, and ionic components in cell, tissue, blood, and other samples. Single-spin columns efficiently absorb and retain cellular debris and sample contaminants while allowing nucleic acids to pass through, reducing the number of steps and plastic materials required for purification. This novel method for high-quality purification is made possible by our innovative SmartLyse® Protease, which enables fast and efficient lysis of a wide range of sample types.
Isolate nucleic acid in a fraction of time compared to traditional silica bind-wash-elute procedures. Simply mix sample with lysis components and incubate according to kit protocol, pipette sample onto the spin column, and centrifuge directly into a collection tube. Cellular debris and contaminants remain bound in the column to be discarded, while purified DNA is ready to be used in downstream applications or stored.
Application
Features and Benefits
Other Notes
Legal Information
Solo come componenti del kit
- Erythrocyte Lysis Buffer
- Blood Lysis Buffer HY
- SmartLyse® HY Protease
- Clearing Solution HY
- 1x Tris Buffer
- Spin Columns
signalword
Danger
Hazard Classifications
Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Met. Corr. 1 - Resp. Sens. 1
Classe di stoccaggio
3 - Flammable liquids
wgk
WGK 3
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Articoli
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.
Contenuto correlato
Animation showing technology principle of GenElute™-E single spin negative chromatography nucleic acid purification kits
Demo video showing how to purify DNA and RNA GenElute™-E single spin nucleic acid purification kits
Answers to frequently asked questions related to GenElute™-E single spin DNA and RNA purification and negative chromatography
Reduce plastic waste and eliminate hazardous liquid waste for more sustainable laboratories with GenElute™-E Single Spin DNA and RNA prep kits.
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What is the composition of the lysis buffer and clearing buffer after flowing through the resin?
1 answer-
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.
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).
Helpful?
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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.
Helpful?
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