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MilliporeSigma

NA1111

GenElute Gel Extraction Kit

sufficient for 70 purifications

Synonym(s):

gel purification kit, Rapid purification of linear DNA

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1 KIT

$170.00

$170.00


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About This Item

UNSPSC Code:
41105501
NACRES:
NA.52

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usage

sufficient for 70 purifications

technique(s)

DNA purification: suitable

storage temp.

15-25°C

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This Item
PLN70PLN350PLX15
technique(s)

DNA purification: suitable

technique(s)

DNA purification: suitable

technique(s)

DNA purification: suitable

technique(s)

DNA purification: suitable

usage

sufficient for 70 purifications

usage

sufficient for 70 purifications

usage

sufficient for 350 purifications

usage

sufficient for 15 purifications

storage temp.

15-25°C

storage temp.

15-25°C

storage temp.

15-25°C

storage temp.

15-25°C

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

General description

The GenElute Gel Extraction Kit is designed for the rapid purification of linear and plasmid DNA fragments from standard or low-melting agarose gels. This kit can also be used to purify DNA from polyacrylamide gels. Typical recovery of DNA is up to 80%. Each column can bind up to 10 μg of DNA from up to a 3.5 g agarose slice.

Application

GenElute Gel Extraction Kit has been used for the purification of DNA fragments from agarose gels.[1][2][3]
The isolated DNA is suitable for a variety of downstream applications, such as sequencing, PCR, restriction digestion, cloning and labeling.

Biochem/physiol Actions

The GenElute Gel Extraction Kit combines silica-binding technology with the convenience of a spin or vacuum column format. DNA fragments of interest are extracted from slices of an agarose gel and are bound to a silica membrane. Contaminants are removed by a simple spin or vacuum wash. The bound DNA is then eluted.

The purified DNA is suitable for a variety of downstream applications, such as automated DNA sequencing, PCR, restriction digestion, cloning, and labeling.
The GenElute Gel Extraction Kit combines silica-binding technology with the convenience of a spin or vacuum column format. DNA fragments of interest are extracted by solubilizing slices of an agarose gel. The Gel Solubilization Solution dissolves an agarose gel slice from gels run in TBE or TAE buffer. The extracted DNA fragments selectively adsorb onto the silica membrane in the presence of the Gel Solubilization Solution. Contaminants are removed by a simple spin or vacuum wash. Finally, the bound DNA is eluted in Tris buffer.

Features and Benefits

  • Bind up to 10 μg of DNA
  • Recoveries up to 80%
  • Up to 3.5 g can be processed per column
  • Compatible with both standard and low-melting agarose in TAE or TBE buffer

Legal Information

GenElute is a trademark of Sigma-Aldrich Co. LLC

Kit Components Only

Product No.
Description

  • Gel Solubilization Solution

  • Elution Solution (10 mM Tris-HCl, pH 9.0)

Kit Components Also Available Separately

Product No.
Description
SDS

  • C2112Column Preparation SolutionSDS

related product

Product No.
Description
Pricing

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1C - STOT SE 3

target_organs

Respiratory system

supp_hazards

Storage Class

8A - Combustible corrosive hazardous materials

flash_point_f

Not applicable

flash_point_c

Not applicable


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Daniel Pérez-Mendoza et al.
Journal of bacteriology, 188(21), 7488-7499 (2006-08-19)
Genetic and biochemical characterization of TraA, the relaxase of symbiotic plasmid pRetCFN42d from Rhizobium etli, is described. After purifying the relaxase domain (N265TraA), we demonstrated nic binding and cleavage activity in vitro and thus characterized for the first time the
Sara N Mitchell et al.
PloS one, 9(3), e92662-e92662 (2014-03-29)
The development of resistance to insecticides has become a classic exemplar of evolution occurring within human time scales. In this study we demonstrate how resistance to DDT in the major African malaria vector Anopheles gambiae is a result of both
Cassandra M Barrett et al.
International journal of molecular sciences, 21(2) (2020-01-18)
A persistent challenge for mammalian cell engineering is the undesirable epigenetic silencing of transgenes. Foreign DNA can be incorporated into closed chromatin before and after it has been integrated into a host cell's genome. To identify elements that mitigate epigenetic
K Michael Lee et al.
Yeast (Chichester, England), 22(6), 431-440 (2005-04-26)
The Saccharomyces cerevisiae ADH2 promoter (P(ADH2)) is repressed several hundred-fold in the presence of glucose; transcription is initiated once the glucose in the medium is exhausted. The promoter can thus be utilized for effective regulation of recombinant gene expression in
Attempts to Construct an Enlarged pUC19 via Insertion of HindIII-digested Coliphage ? DNA
Muhamed Amirie
Journal of Experimental Microbiology and Immunology, 18, 96-101 (2014)

Protocols

The GenElute Gel Extraction kit is designed for the rapid purification of 50 bp to 10 kb linear DNA fragments and plasmids from standard or low-melting agarose gels.

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