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.
Größe auswählen
€ 43,90
€ 191,00
€ 857,00
Über diesen Artikel
Fortfahren mit
purified by
(Single-spin negative chromotography), (Time: 3 minutes or less)
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.)
greener alternative product characteristics
Waste Prevention
Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
technique(s)
RNA purification: suitable
input
DNA
test parameters
: 3 min hands on time, sample volume: 90-110 μL
greener alternative category
storage temp.
room temp
1 of 4
Dieser Artikel | |||
|---|---|---|---|
| storage temp. room temp | storage temp. room temp | storage temp. room temp | storage temp. - |
| purified by (Single-spin negative chromotography) | 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: 45 minutes or less) |
| feature Compatible Application (Suitable for most common downstream applications, including RT-PCR, gene expression, and NGS) | 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 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.) | 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.) |
| greener alternative product characteristics Waste Prevention | greener alternative product characteristics Waste Prevention | greener alternative product characteristics Waste Prevention | greener alternative product characteristics Waste Prevention |
| sustainability Greener Alternative Product | sustainability Greener Alternative Product | sustainability Greener Alternative Product | sustainability Greener Alternative Product |
| greener alternative category | greener alternative category , Aligned | greener alternative category | greener alternative category |
General description
GenElute™-E kits are based on the principle of negative chromatography, where impurities like salt, detergent, proteins and organic solvents are removed by the column material and the purified nucleic acid is collected in the flow-through in just one single centrifugation step. This convenient procedure enables a significantly faster purification of nucleic acid samples than standard bind-wash-elute procedures, with less handling, drastically reduced plastic consumable usage, and no use of hazardous materials like chaotropic salts or organic solvents.
With conventional methods, traces of chaotropic salt and ethanol are usually coeluted with these purification procedures, which often leads to inhibition of real-time PCR experiments. GenElute™-E kits do not contain any chaotropic salts, organic solvents or EDTA, resulting in improved performance in downstream applications such as RT-PCR, gene expression, and NGS.
Because of the negative chromatography principle, there is no limitation to the amount of DNA that is cleaned up. Maximum sample volume is 100 μl. The purified nucleic acid is eluted in water and can immediately be used for downstream applications. A 1x TE Buffer, pH 8.5, is supplied to enable storage of samples.
Application
Features and Benefits
Other Notes
Legal Information
Nur Kit-Komponenten
- RNA Cleanup Spin Columns
- 1x Tris Buffer
Lagerklasse
10 - Combustible liquids
wgk
WGK 3
Hier finden Sie alle aktuellen Versionen:
Besitzen Sie dieses Produkt bereits?
In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.
Artikel
Auswirkungen der Aufreinigungsmethode auf die Genauigkeit der DNA-Quantifizierung und nachgeschaltete enzymatische Prozesse Bewertung der Reinheit genomischer DNA durch UV-Spektralphotometrie, Gelelektrophorese und nachgeschaltete qPCR bei Verwendung von GenElute™-E DNA-Aufreinigungskits.
Verwandter Inhalt
KOD One™ PCR Master Mix overview for ultra-fast PCR with high specificity, fidelity, and yield
Animation zur Veranschaulichung des technologischen Prinzips der GenElute™-E Negativ-Chromatographie Nukleinsäure-Aufreinigungskits für einzelne Spins
Demo-Video zur Aufreinigung von DNA und RNA mit GenElute™-E Kits für die Einzel-Spin Aufreinigung von Nukleinsäuren
Antworten auf häufig gestellte Fragen (FAQ) zur GenElute™-E Einzel-Spin DNA-/RNA-Aufreinigung und Negativ-Chromatographie
Global Trade Item Number
| SKU | GTIN |
|---|---|
| EC800-50RXN | 04061842202843 |
| EC800-250RXN | 04061842202850 |
| EC800-10RXN | 04061842202836 |
-
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?
-
-
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?
-
-
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?
-
-
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.
Helpful?
-
-
Is there a minimum value for using this kit? I have eight samples with RNA concentrations ranging from 5 to 14 ug. Does the kit work for me? How much RNA will lose during the procedure?
1 answer-
The key driver for yield in the GenElute-E kits is the fragment length, as this product utilizes a fractionation method. The expected yield should be greater than 80% as long as the sample is within a 50-100 µL load and greater than 50 bases.
Helpful?
-
Active Filters
Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..
Setzen Sie sich mit dem technischen Dienst in Verbindung


