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LSKGEL050

Millipore

Montage Gel Extraction Kit

DNA Gel Extraction

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Synonym(s):
Ultrafree-DA
eCl@ss:
32039006

material

polypropylene

Quality Level

manufacturer/tradename

Montage®

application(s)

genomic analysis

shipped in

ambient

Related Categories

General description

Recover 100 to 10,000 bp DNA from agarose gel slices in a single 10-minute spin. The kit consists of a pre-assembled filter device with an agarose gel nebulizer, a microcentrifuge vial, and modified TAE gel extraction buffer (dry).

The device utilizes gel compression to extract DNA from the agarose. Centrifugal force collapses the gel structure, drives the agarose through a small orifice in the gel nebulizer and the resultant gel slurry is sprayed into the sample filter cup.

Prepared DNA requires no further purification for most applications, including cloning and radioisotopic or fluorescent DNA sequencing. Since agarose gel electrophoresis has high resolving power, the small and large non-specific amplification products that frequently interfere with cloning and sequencing after PCR are completely removed from the product.

  • Minimal hands-on time
  • 10-minute spin
  • Fully-functional DNA


Performance
Typical DNA Recoveries from Agarose Gels

DNA Size (bp) Percent DNA Recoveries

100 78
700 71
1000 77
2027 47
4361 35
9416 32
23130 29

Protocol
1. Excise the band of interest after routine electrophoretic analysis of PCR products or other DNA through an agarose gel.
2. Place the gel slice into the pre-assembled device. Note: Protocol is not compatible with low melting point agarose.
3. Spin at 5,000 x g for 10 minutes to extract gel slurry into filter cup.
4. DNA can be stored in the capped filtrate vial after discarding the sample filter cup and gel nebulizer.

Components

includes 50 Ultrafree-DA devices and 500 mL of 50x concentrated modified TAE Buffer

Legal Information

MONTAGE is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

10 - Combustible liquids

WGK

WGK 1


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Stephen Wandro et al.
mSphere, 3(3) (2018-06-08)
The assembly and development of the gut microbiome in infants have important consequences for immediate and long-term health. Preterm infants represent an abnormal case for bacterial colonization because of early exposure to bacteria and frequent use of antibiotics. To better
Hung-Ju Hsu et al.
Structure (London, England : 1993), 14(10), 1499-1510 (2006-10-10)
Structure propensities of amino acids are important determinants in guiding proteins' local and global structure formation. We constructed a phage display library--a hexa-HIS tag upstream of a CXXC (X stands for any of the 20 natural amino acids) motif appending
Sarah D Perkins et al.
Applied and environmental microbiology, 75(16), 5363-5372 (2009-07-08)
Potential pathogens from shower water and aerosolized shower mist (i.e., shower aerosol) have been suggested as an environmental source of infection for immunocompromised patients. To quantify the microbial load in shower water and aerosol samples, we used culture, microscopic, and
Stig Mølgaard Rask Jensen et al.
PloS one, 7(8), e43095-e43095 (2012-08-23)
Gene silencing by RNA interference (RNAi) can be achieved by the ectopic expression of tailored short hairpin RNAs (shRNAs) which after export to the cytoplasm are processed by Dicer and incorporated into the RNA induced silencing complex (RISC). Design rules
Arman Kulyyassov et al.
Life (Basel, Switzerland), 12(2) (2022-02-26)
Protein tags are peptide sequences genetically embedded into a recombinant protein for various purposes, such as affinity purification, Western blotting, and immunofluorescence. Another recent application of peptide tags is in vivo labeling and analysis of protein-protein interactions (PPI) by proteomics

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